[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"geriatric\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:geriatric":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,25,0,[8,48,85,112,139,173,207,228,249,271,291,312,341,371,410,434,459,488,512,531,554,587,615,653,679],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":17,"targetDuration":4,"studyType":20,"phases":21,"briefSummary":23,"conditions":24,"keywords":29,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":4},"100628162","comparson-of-the-effcacy-of-conventonal-exercse-and-plates-n-pre-fral-and-fral-older-adults-100628162",false,"NCT07458048","Comparıson of the Effıcacy of Conventıonal Exercıse and Pılates ın Pre-fraıl and Fraıl Older Adults","Inclusion Criteria:\n\n* Age 60 years and older Classified as prefrail or frail according to the FRAIL Scale A score of 24 or higher on the Mini-Mental State Examination (MMSE) Provided written informed consent after being informed about the study\n\nExclusion Criteria:\n\nPresence of unstable cardiovascular disease Having received physical therapy and rehabilitation within the past 6 months History of severe neurological disorders History of major surgery affecting mobility within the past 6-12 months Severe musculoskeletal or orthopedic conditions that limit or preventt independent mobility.\n\n\\-","ALL","60 Years",{"count":18,"type":19},40,"ESTIMATED","INTERVENTIONAL",[22],"NA","Brief Summary\n\nThis clinical study aims to compare the effects of a conventional exercise program and a Pilates exercise program in prefrail and frail older adults. A total of 40 participants aged 60 years and older who are classified as prefrail or frail according to the FRAIL Scale will be included in the study.\n\nParticipants will be randomly assigned to either the conventional exercise group or the Pilates group. Both exercise programs will be conducted twice weekly for 6 weeks. The interventions will focus on stretching exercises, balance and perturbation training, and strength exercises targeting major muscle groups.\n\nPrimary outcomes will include changes in frailty status assessed before and after the intervention. Secondary outcomes will include functional mobility and balance assessed by the Timed Up and Go Test, dynamic balance assessed by the Functional Reach Test, lower extremity strength assessed by the 30-Second Sit-to-Stand Test, gait speed assessed by the 10-Meter Walk Test, depressive symptoms and psychological well-being assessed by the Yesavage Geriatric Depression Scale, independence in daily activities assessed by the Lawton Instrumental Activities of Daily Living Scale, cognitive status assessed by the Mini-Mental State Examination, and fatigue assessed by the Modified Borg Scale. Frailty status will be evaluated using the FRAIL Scale.\n\nThroughout the study, participant safety will be monitored, and any adverse events, such as injuries or discomfort occurring during exercise sessions, will be recorded and managed appropriately.\n\nThis study is expected to provide valuable clinical evidence regarding the effectiveness of conventional exercise and Pilates programs in improving physical health and reducing frailty in prefrail and frail older adults, thereby contributing to the identification of best practice approaches for the management of this vulnerable population.",[25,26,27,28],"Frailty Syndrome","Prefrail Elderly","Frail Elderly","Geriatric",[30,31,32,33,34,35],"Pilates","geriatric","conventional","frailty","exercises","prefrail","NOT_YET_RECRUITING","2026-06-20",{"date":39,"type":40},"2026-06-25","ACTUAL",{"date":42,"type":19},"2026-06-22",{"date":44,"type":19},"2027-02",{"name":46,"class":47},"Istanbul University - Cerrahpasa","OTHER",{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":54,"eligibilityCriteria":55,"healthyVolunteers":56,"sex":15,"minAge":57,"maxAge":58,"enrollmentInfo":59,"targetDuration":4,"studyType":20,"phases":60,"briefSummary":61,"conditions":62,"keywords":70,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":75,"lastUpdatePostDateStruct":76,"startDateStruct":78,"completionDateStruct":80,"leadSponsor":82,"locationsCount":84},"100643382","the-act-on-a-geriatric-5-ms-guided-physical-therapy-intervention-for-knee-osteo-arthritis-in-older-adults-100643382","NCT07640529","The ACT-ON: A Geriatric 5-Ms-Guided Physical Therapy Intervention for Knee Osteo-Arthritis in Older Adults.","The ACT-ON: A Geriatric 5-Ms-Guided Physical Therapy Intervention for Knee Osteo-Arthritis in Older Adults: A Randomised Control Trial","5Ms\u002FPT\u002FKOA\u002FOA","Inclusion Criteria:\n\n* Prospective participants will be Saudi Nationals\n* aged 60 years or older\n* with a clinical diagnosis of knee osteoarthritis.\n* individuals must be capable of walking 10 meters independently or with an assistive device\n* self-report the ability to tolerate a one-hour assessment session.\n\nExclusion Criteria:\n\n* severe cognitive impairment\n* knee surgery within the past 6 months.\n* diagnosis of rheumatoid arthritis\n* the presence of unstable comorbidities (e.g., uncontrolled hypertension, heart failure, arrhythmia, severe pulmonary disease requiring oxygen, or a cardiac event in the past 6 months).\n* severe joint instability or deformity.\n* unmanaged severe osteoporosis.\n* a recent intra-articular corticosteroid injection (\\\u003C3 months).\n* active cancer treatment within the past 6 months.\n* non-elective hospitalization for a major illness.\n* surgery within the past 6 months.",true,"55 Years","90 Years",{"count":18,"type":19},[22],"The study is a Random control trail study conducted at King Khalid University Hospital in Riyadh, Saudi Arabia, focusing on Application of 5 framework in rehabilitation program of knee arthritis. The study will involve a in each group sample of 20 KOA patients, with a 12-month duration. The sample size was estimated using G\\*Power 3.1 software, and the initial power analysis indicated that 40 participants would be required to achieve 80.0% statistical power. The study's participants will be aged between 55 and 80 years, diagnosed with Knee osteoarthritis, without cognitive impairment, knee surgery in the past 6 months, or unstable comorbidities. The study will involve in-person 16 sessions, with the first two lasting approximately one hour and the remaining session 30-45 minutes. The main outcome measures that will be used in this study are Stay Independent Brochure, Iconographical Falls Efficacy Scale (icon-FES), Timed Up and Go, 2-Minute Walk Test, 5 Time Set to Stand Test AND Arthritis Self-Efficacy Scale 8 Item (ASES-8), Patient-Specific Functional Scale (PSFS), and Patient satisfaction level with Physical Therapy service MedRisk. Data will be taken from direct questions to patients, by filling out the questionnaire via Google Form, and through some tests and SPSS will be used for data analysis, with ANOVA Test intervention scores of the outcome measures.",[63,64,28,65,66,67,68,69],"Rehabilitation","Excercise","Physical Therapy","Rehabilitation Exercise","Rehabilitation Outcome","Knee Osteoarthristis","Knee Osteoarthritis",[71,72,73,74],"5Ms","PT","KOA","OA","2026-06-06",{"date":77,"type":40},"2026-06-10",{"date":79,"type":19},"2026-05-15",{"date":81,"type":19},"2026-10-15",{"name":83,"class":47},"King Saud University",1,{"id":86,"slug":87,"hasResults":11,"nctId":88,"briefTitle":89,"officialTitle":90,"acronym":4,"eligibilityCriteria":91,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":92,"targetDuration":4,"studyType":20,"phases":94,"briefSummary":95,"conditions":96,"keywords":98,"overallStatus":101,"whyStopped":4,"lastUpdateSubmitDate":102,"lastUpdatePostDateStruct":103,"startDateStruct":105,"completionDateStruct":107,"leadSponsor":109,"locationsCount":84},"100591778","effect-of-enzymatic-containing-mouth-spray-oral7-on-xerostomia-symptoms-salivary-flow-rate-and-oral-health-related-quality-of-life-in-older-patients-100591778","NCT06984848","Effect of Enzymatic-Containing Mouth Spray (Oral7®) on Xerostomia Symptoms, Salivary Flow Rate, and Oral Health-Related Quality of Life in Older Patients","Effect of Enzymatic-Containing Mouth Spray (Oral7®) on Xerostomia Symptoms, Salivary Flow Rate, and Oral Health-Related Quality of Life in Older Patients: A Randomised Placebo-Control Trial","Inclusion Criteria:\n\n* Aged 60 years and above\n* Patients with often or always having dry mouth\u002Fxerostomia by asking single-item xerostomia question: \"How often does your mouth feel dry?\" (Adakah mulut anda sering merasakan kekeringan?). The response options were \"Never (Tidak Pernah),\" \"Sometimes (Kadang-kadang),\" \"Often (Kerap),\" or \"Always (Sentiasa\u002FSepanjang masa).\"\n* Patients who are taking nutrition orally\n* Patients who are able to speak\n* Patients who are physically fit to take oral spray on their own.\n\nExclusion Criteria:\n\n* • Patients on salivary substitutes for the past one week\n\n  * Oral condition that required immediate attention such as mucosal or gingival bleeding, orofacial swelling, oral pain and oral ulcer.\n  * Patients who are deaf and mute\n  * Those with mental disabilities or documented cognitive deficits that would impair their ability to answer questions independently.",{"count":93,"type":19},100,[22],"Background: Xerostomia, or dry mouth, is a prevalent condition among older adults and has significant implications for oral and systemic health. It is associated with impaired chewing, swallowing, and speech, and increases the risk of oral infections, dental caries, and gum disease. Xerostomia may also contribute to malnutrition and aspiration pneumonia.\n\nObjective: This study aims to evaluate the effectiveness of an enzymatic-containing mouth spray (Oral7®) on xerostomia symptoms, unstimulated salivary flow rate, and oral health-related quality of life (OHRQoL) in older patients with xerostomia.\n\nMethods: A single-center, randomized, double-blind, placebo-controlled trial will be conducted at Hospital Universiti Sains Malaysia from August 2025 to July 2026. Eligible participants aged 60 and above with self-reported xerostomia will be randomly assigned to receive either Oral7® Mouth Spray or a placebo spray for four weeks. The primary outcome is the mean change in Summated Xerostomia Inventory (SXI) scores between groups from baseline to post-intervention. Secondary outcomes include changes in unstimulated salivary flow rate using the sialometry technique and OHRQoL measured by the Geriatric Oral Health Assessment Index (GOHAI) at baseline and three months post-intervention. Data will be analyzed using SPSS version 29.\n\nConclusion: This trial will provide evidence on the efficacy of Oral7® Mouth Spray in alleviating xerostomia symptoms and improving salivary function and oral health-related quality of life in older adults, potentially guiding future clinical management of this condition.",[97,28],"Xerostomia",[97,99,31,100],"dry mouth","older patient","RECRUITING","2026-05-20",{"date":104,"type":40},"2026-05-22",{"date":106,"type":40},"2025-09-18",{"date":108,"type":19},"2027-05-01",{"name":110,"class":111},"ZAINAB MAT YUDIN","INDUSTRY",{"id":113,"slug":114,"hasResults":11,"nctId":115,"briefTitle":116,"officialTitle":117,"acronym":4,"eligibilityCriteria":118,"healthyVolunteers":56,"sex":15,"minAge":119,"maxAge":4,"enrollmentInfo":120,"targetDuration":121,"studyType":122,"phases":4,"briefSummary":123,"conditions":124,"keywords":127,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":132,"lastUpdatePostDateStruct":133,"startDateStruct":135,"completionDateStruct":136,"leadSponsor":138,"locationsCount":84},"100640366","validity-and-reliability-of-the-turkish-form-of-the-enjoyment-of-physical-activity-scale-8-in-geriatrics-with-minimal-cognitive-impairment-100640366","NCT07588685","Validity and Reliability of the Turkish Form of the Enjoyment of Physical Activity Scale-8 in Geriatrics With Minimal Cognitive Impairment","Validity and Reliability of the Turkish Form of the Enjoyment of Physical Activity Scale-8 (PACES-8) in Geriatric Individuals With Minimal Cognitive Impairment","Inclusion Criteria:\n\n* Being 65 years of age or older,\n* Having a diagnosis of Minimal Cognitive Impairment (MCI),\n* Having a Standardized Mini Mental Test (SMMT) score between 24 and 27 (mild cognitive impairment level),\n* Being largely independent in daily living activities (absence of functional dependency),\n* Being able to mobilize independently,\n* Having the communication level to understand and answer the survey questions,\n* Volunteering to participate in the study and providing written informed consent.\n\nExclusion Criteria:\n\n* Diagnosis of dementia or advanced cognitive impairment,\n* Acute medical conditions that prevent participation in physical activity,\n* Severe vision or hearing loss,\n* Presence of neurological or psychiatric disorders that prevent completion of questionnaire forms,\n* Serious neurological event within the last 6 months (stroke, traumatic brain injury, etc.).","65 Years",{"count":93,"type":19},"1 Week","OBSERVATIONAL","The main objective of this study is to examine the validity and reliability of the Turkish form of the Enjoyment of Physical Activity Scale-8 (PACES-8) in individuals aged 65 and over with Minimal Cognitive Impairment (MCI).",[28,125,126],"Elderly","Cognitive Abnormality",[128,129,130,131],"physical activity","enjoyment","cognitive impairment","elderly","2026-05-14",{"date":134,"type":40},"2026-05-18",{"date":79,"type":19},{"date":137,"type":19},"2026-08-01",{"name":46,"class":47},{"id":140,"slug":141,"hasResults":11,"nctId":142,"briefTitle":143,"officialTitle":144,"acronym":4,"eligibilityCriteria":145,"healthyVolunteers":11,"sex":15,"minAge":119,"maxAge":4,"enrollmentInfo":146,"targetDuration":4,"studyType":20,"phases":148,"briefSummary":149,"conditions":150,"keywords":154,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":163,"lastUpdatePostDateStruct":164,"startDateStruct":166,"completionDateStruct":168,"leadSponsor":170,"locationsCount":4},"100638990","effect-of-lateral-decubitus-position-after-spinal-anesthesia-on-hemodynamic-stability-in-high-risk-geriatric-patients-100638990","NCT07597148","Effect of Lateral Decubitus Position After Spinal Anesthesia on Hemodynamic Stability in High-Risk Geriatric Patients","The Effects of Lateral Decubitus Positioning After Spinal Anesthesia on Hemodynamic Stability in High-Risk Geriatric Patients Undergoing Lower Extremity Orthopedic Surgery: A Prospective Randomized Controlled Trial","Inclusion Criteria:\n\n* Age 65 years or older\n* ASA physical status classification III or IV\n* Scheduled for unilateral lower extremity orthopedic surgery (hip fracture, femur fracture, knee arthroplasty, tibia-fibula fracture, or similar procedures)\n* Eligible for spinal anesthesia\n* Written informed consent obtained\n\nExclusion Criteria:\n\n* Contraindications to spinal anesthesia (coagulopathy, recent anticoagulant or antiplatelet use without adequate washout period, local infection at injection site)\n* Severe neurological disease or pre-existing motor or sensory deficit\n* Significant spinal deformity (severe scoliosis, kyphosis) or history of previous spinal surgery\n* Known allergy to local anesthetics\n* Decompensated heart failure (ejection fraction below 30%)\n* Uncontrolled hypertension (systolic blood pressure above 180 mmHg or diastolic blood pressure above 110 mmHg)\n* Emergency surgery\n* Severe hypovolemia or active bleeding\n* Advanced dementia or inability to communicate\n* Body mass index above 40 kg\u002Fm²\n* Refusal to participate",{"count":147,"type":19},70,[22],"Spinal anesthesia is a common and preferred anesthetic technique for lower extremity orthopedic surgery in elderly patients. However, it can cause a significant drop in blood pressure (hypotension), especially in high-risk older patients with multiple medical conditions. This complication can lead to serious consequences such as heart attack, stroke, or death in vulnerable patients.\n\nThis study investigates whether keeping patients in a lateral (side-lying) position for 15 minutes after spinal anesthesia - instead of immediately turning them onto their back (supine position) - can reduce the risk of hypotension. When a patient lies on their side after receiving spinal anesthesia with a heavy (hyperbaric) local anesthetic, the medication tends to stay concentrated on the lower (operative) side, resulting in a more limited nerve block. This may help preserve blood pressure stability.\n\nWe will enroll 70 patients aged 65 years or older with high anesthetic risk (ASA physical status III or IV) scheduled for unilateral lower extremity orthopedic surgery under spinal anesthesia. Patients will be randomly assigned to two groups: one group will be kept in the lateral decubitus position (operative side down) for 15 minutes before being turned supine, and the other group will be turned supine immediately after spinal anesthesia. Blood pressure, heart rate, and oxygen saturation will be monitored continuously. The primary outcome is the incidence of hypotension during the first 15 minutes after spinal anesthesia.",[151,152,28,153],"Hypotension Drug-Induced","Spinal Aneshtesia","Orthopedic Surgery Patients",[155,156,157,31,158,159,160,161,162],"hypotension","spinal anesthesia","lateral decubitus position","hyperbaric bupivacaine","unilateral spinal block","hemodynamic stability","orthopedic surgery","ASA III-IV","2026-05-12",{"date":165,"type":40},"2026-05-19",{"date":167,"type":19},"2026-06-01",{"date":169,"type":19},"2026-08-10",{"name":171,"class":172},"University of Health Sciences Balikesir Hospital Eduation and Research","OTHER_GOV",{"id":174,"slug":175,"hasResults":11,"nctId":176,"briefTitle":177,"officialTitle":178,"acronym":179,"eligibilityCriteria":180,"healthyVolunteers":56,"sex":15,"minAge":119,"maxAge":4,"enrollmentInfo":181,"targetDuration":4,"studyType":20,"phases":183,"briefSummary":184,"conditions":185,"keywords":190,"overallStatus":101,"whyStopped":4,"lastUpdateSubmitDate":199,"lastUpdatePostDateStruct":200,"startDateStruct":201,"completionDateStruct":203,"leadSponsor":205,"locationsCount":84},"100625207","this-study-investigates--hydroxy--methylbutyrate-hmb-and-2-hydroxybenzylamine-2-hoba-when-administered-either-individually-or-in-combination-contributes-to-an-increased-quality-of-health-specifically-improving-muscular-strength-and-cognitive-functioning-in-adults-over-the-age-of-65-100625207","NCT07419633","This Study Investigates β-hydroxy-β-methylbutyrate (HMB) and 2-hydroxybenzylamine (2-HOBA), When Administered Either Individually or in Combination Contributes to an Increased Quality of Health, Specifically Improving Muscular Strength and Cognitive Functioning in Adults Over the Age of 65.","The Effects of Beta-Hydroxy-Beta-methylbutyrate (HMB) and\u002For 2-hydroxybenzylamine (2-HOBA) on Markers of Health Span in Older Adults. A Randomized Control Trial.","H2AGE","Inclusion Criteria:\n\n•. 65 years of age\n\n* English or French speaking\n* Females not of childbearing potential\n* Willing to maintain current lifestyle and dietary habits, including level of physical activity, allowed medication\u002Fsupplements habits for the duration of the study\n\nExclusion Criteria:\n\n* Known cardiac diseases, known arterial fibrillation, hepatic diseases, immune diseases (e.g. Individuals with an acute infectious disease, autoimmune disease or are immune compromised), ulcers, asthma, gout, severe anemia, hay fever, nasal polyps.\n\n  * Chronic kidney disease \\[estimated glomerular filtration rate (GFR) \\\u003C 35 mL\u002Fmin\\].\n  * Neurological injury\u002Fdisorder with significant persistent neurological or functional deficit (e.g., stroke with hemiparesis, spinal cord injury, muscular dystrophy, myopathy, myasthenia gravis, Parkinson's disease, peripheral polyneuropathy).\n  * Neuropsychological condition and\u002For cognitive impairment that, in the QI's opinion, could interfere with study participation\n  * History of confirmed chronic obstructive pulmonary disease with a severity grade \\> 2 on the Medical Research Council Dyspnea Scale.\n  * Uncontrolled hypothyroidism or hyperthyroidism. Hypothyroid patients who have changed their dose of hormone replacement therapy in the 6 weeks before screening are not eligible.\n  * Underlying muscle diseases, including a history of or currently active myopathy (e.g., dermatomyositis, polymyositis, etc.) or muscular dystrophies.\n  * Confirmed rheumatoid arthritis, acquired immunodeficiency syndrome (AIDS), type 1 or type 2 diabetes mellitus.\n  * History of cancer in the last 6 months.\n  * Not on any medications including NHPs\u002Fliving with medical conditions that would compromise the study outcome or the safety of the research participant.\n  * Known allergy to study medication or its components (non-medicinal ingredients).\n  * Allergy to aspirin\u002Fsalicylate or if using other drugs containing acetylsalicylic acid or other salicylates and a history of ASA-sensitive asthma\u002Fbronchospasm\n\nThe following list of medications\u002FNHPs will be excluded (and weaned as seen necessary by the study physician) prior to and during the study:\n\n* Participants on newly initiated cholesterol-lowering medication will be excluded. Those on stable regimens for ≥3 months will be included and will be monitored for potential interactions as per the HMB monograph.\n* Medications associated with muscle weakness or immune effects (i.e., oral glucocorticoids).\n* Medications or supplements affecting skeletal muscle metabolism or weight including: Use of MAO-I's (monoamine oxidase inhibitors), additional consumption of 2-HOBA, Vitamin D or HMB, anabolic steroids, selective androgen receptor modulators (SARMs), corticosteroids, GLP-1s, or other weight loss medications).\n* Excessive protein supplementation (i.e., \\>2.0 g\u002Fkg\u002Fday).\n* All participants must be on a stable dose of allowed supplements\u002Fmedications for at least 3 months prior to enrollment. All concomitant therapies will be documented.\n\nNon-pharmacological interventions that could influence study outcomes (e.g., pulmonary rehabilitation, structured exercise programs) will not be permitted.\n\nParticipants undergoing such therapies will be excluded. Any new interventions started during the study must be reported and if judged inappropriate, will result in withdrawal from the trial.",{"count":182,"type":19},120,[22],"In this study, participants will be assigned to receive HMB, 2-HOBA, a combination of both, or a comparison supplement for a set period of time. During the study, participants will attend scheduled visits where researchers will assess muscle strength, physical function, and overall health. Blood samples may be collected to measure markers related to metabolism, inflammation, and oxidative stress. Study staff will also monitor safety and any side effects throughout the study.",[186,187,28,188,189],"Muscle","Cognitive Functioning","Ageing and Geriatric Health","Ageing",[191,186,192,193,194,195,196,197,198],"Health","Cognitive","Memory","natural product","ageing","natural","supplement","preservation","2026-05-11",{"date":132,"type":40},{"date":202,"type":40},"2026-03-06",{"date":204,"type":19},"2027-02-05",{"name":206,"class":47},"McGill University Health Centre\u002FResearch Institute of the McGill University Health Centre",{"id":208,"slug":209,"hasResults":11,"nctId":210,"briefTitle":211,"officialTitle":211,"acronym":4,"eligibilityCriteria":212,"healthyVolunteers":56,"sex":15,"minAge":119,"maxAge":4,"enrollmentInfo":213,"targetDuration":121,"studyType":122,"phases":4,"briefSummary":215,"conditions":216,"keywords":217,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":221,"lastUpdatePostDateStruct":222,"startDateStruct":224,"completionDateStruct":226,"leadSponsor":227,"locationsCount":84},"100636222","validity-and-reliability-of-the-exercise-related-health-beliefs-attitude-scale-in-geriatric-individuals-100636222","NCT07562880","Validity and Reliability of the Exercise-Related Health Beliefs Attitude Scale in Geriatric Individuals","Inclusion Criteria:\n\n* Being 65 years of age or older,\n* Volunteering to participate in the research\n* Not having a disease that affects cognitive function\n* Being able to understand the questions asked by the researchers\n* Volunteering\n\nExclusion Criteria:\n\n* Severe vision\u002Fhearing loss,\n* Having cognitive diseases such as dementia, Alzheimer's, etc.\n* Inability to walk\n* Not being a volunteer",{"count":214,"type":19},200,"The main purpose of this research is to test the validity and reliability of the \"Exercise Health Beliefs Attitude Scale\" (EYSİTÖ), developed by Caz, Paktaş and Yazıcı (2023) for adult individuals, in geriatric individuals aged 65 and over.",[28,125],[218,219,220,131],"exercise behavior","pyhsical activity","motivatıon","2026-05-09",{"date":223,"type":40},"2026-05-13",{"date":225,"type":19},"2026-05-05",{"date":137,"type":19},{"name":46,"class":47},{"id":229,"slug":230,"hasResults":11,"nctId":231,"briefTitle":232,"officialTitle":233,"acronym":4,"eligibilityCriteria":234,"healthyVolunteers":56,"sex":15,"minAge":119,"maxAge":4,"enrollmentInfo":235,"targetDuration":236,"studyType":122,"phases":4,"briefSummary":237,"conditions":238,"keywords":239,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":221,"lastUpdatePostDateStruct":244,"startDateStruct":245,"completionDateStruct":247,"leadSponsor":248,"locationsCount":84},"100636220","comparison-of-hand-grip-strength-in-different-shoulder-positions-in-geriatric-individuals-position-dependent-strength-analysis-100636220","NCT07562854","Comparison of Hand Grip Strength in Different Shoulder Positions in Geriatric Individuals: Position-Dependent Strength Analysis","Comparison of Hand Grip Strength in Different Shoulder Positions in Geriatric Individuals: Position-Dependent Strength Analysis - A Cross-Sectional Analytical Study With Repeated Measurements","Inclusion Criteria:\n\n* Being 65 years of age or older\n* Being an independent volunteer living in the community\n* Being able to actively use the upper extremities\n* Having the cognitive level to understand and follow the measurement instructions\n* Providing written informed consent to participate in the study.\n\nExclusion Criteria:\n\n* Presence of severe shoulder pain or rotator cuff pathology\n* Loss of upper extremity function due to rheumatological disease\n* Presence of significant visual or vestibular impairment that may affect measurements\n* Presence of another systemic or musculoskeletal disease that may prevent the safe and accurate completion of tests\n* History of upper extremity surgery or fracture within the last 6 months\n* Failure to provide informed consent",{"count":18,"type":19},"1 Day","The aim of this study is to examine the relationship between hand grip strength, measured in different shoulder positions, and upper extremity muscle strength, and to reveal the clinical significance of position-dependent strength variation.",[28,125],[240,241,242,243],"muscle strenght","hand grip strength","geriatrics","upper extremity muscle strength",{"date":223,"type":40},{"date":246,"type":19},"2026-05-02",{"date":137,"type":19},{"name":46,"class":47},{"id":250,"slug":251,"hasResults":11,"nctId":252,"briefTitle":253,"officialTitle":254,"acronym":4,"eligibilityCriteria":255,"healthyVolunteers":56,"sex":15,"minAge":119,"maxAge":4,"enrollmentInfo":256,"targetDuration":121,"studyType":122,"phases":4,"briefSummary":258,"conditions":259,"keywords":261,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":264,"lastUpdatePostDateStruct":265,"startDateStruct":267,"completionDateStruct":268,"leadSponsor":270,"locationsCount":84},"100636225","comparison-of-physical-performance-balance-and-functional-mobility-parameters-according-to-walking-speed-in-geriatric-individuals-100636225","NCT07562919","Comparison of Physical Performance, Balance, and Functional Mobility Parameters According to Walking Speed in Geriatric Individuals","Comparison of Physical Performance, Balance, and Functional Mobility Parameters According to Walking Speed Threshold Values in Geriatric Individuals","Inclusion Criteria:\n\n* Being 65 years of age or older\n* Being able to perform walking functions\n* Having sufficient mobility to perform the physical performance tests included in the research, such as 5 sit-stand tests, TUG (Trip and Go) tests, and stair climbing\u002Fdescending tests. • Having a walking speed of at least 0.4 m\u002Fs or more as a result of the 4 Meter Walking Test (having limited or independent mobility within the community).\n* Voluntarily agreeing to participate in the study and providing informed consent.\n\nExclusion Criteria:\n\n1. Having a history of advanced cognitive impairment or diagnosed dementia that would impair the ability to understand and follow test instructions.\n2. Those diagnosed with moderate or severe cognitive impairment (MMSE \\\u003C 24 and\u002For MoCA \\\u003C 21)\n3. Having a walking speed below 0.4 m\u002Fs on the 4-Meter Walk Test (individuals who are wheelchair-bound or bedridden).\n4. Advanced Parkinson's disease, active stroke sequelae, lower extremity fracture within the last 6 months, or a history of acute orthopedic surgery that primarily affects motor performance and balance.\n5. Those with severe hearing or vision loss\n6. Individuals experiencing significant difficulty communicating\n7. Participants who did not sign the voluntary consent form",{"count":257,"type":19},76,"The aim of this study is to examine the determining role of walking speed on physical performance parameters in individuals aged 65 and over. The study aims to compare flexibility, lower extremity muscle strength (5-count sit-stand test), static balance (single-leg balance), upper extremity muscle strength (hand grip), dynamic balance (FUT), functional mobility (TUG), and stair climbing\u002Fclimbing skills in individuals with walking speeds of 0.4-0.8 m\u002Fs (limited community mobility) and above 0.8 m\u002Fs (independent community mobility).",[28,260],"Elderly (People Aged 65 or More)",[262,263,31,131],"walkinp speed","physical fıtness","2026-04-25",{"date":266,"type":40},"2026-05-01",{"date":266,"type":19},{"date":269,"type":19},"2026-08-30",{"name":46,"class":47},{"id":272,"slug":273,"hasResults":11,"nctId":274,"briefTitle":275,"officialTitle":276,"acronym":4,"eligibilityCriteria":277,"healthyVolunteers":56,"sex":15,"minAge":4,"maxAge":4,"enrollmentInfo":278,"targetDuration":121,"studyType":122,"phases":4,"briefSummary":280,"conditions":281,"keywords":282,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":264,"lastUpdatePostDateStruct":286,"startDateStruct":287,"completionDateStruct":289,"leadSponsor":290,"locationsCount":84},"100636223","evaluating-the-clinical-suitability-of-microsoft-xbox-one-games-in-geriatric-rehabilitation-100636223","NCT07562893","Evaluating the Clinical Suitability of Microsoft Xbox One Games in Geriatric Rehabilitation","Evaluating the Clinical Suitability of Microsoft Xbox One Games in Geriatric Rehabilitation: A Delphi Study","Inclusion Criteria:\n\n1. To be a Physiotherapist with at least 5 years of clinical\u002Facademic experience in geriatric rehabilitation or neurological rehabilitation,\n2. To be a researcher in game technologies, Exergame applications, or Kinect systems, and to be a Physiotherapist with clinical\u002Facademic experience,\n3. To approve the 'Informed Consent Form' regarding participation in the study.\n\nExclusion Criteria:\n\n1. Not having conducted research\u002Facademic activities in the specified areas of expertise (Physiotherapy, Gerontology, Play Technologies),\n2. Failure to provide feedback within the specified timeframes,\n3. Withdrawing voluntarily at any stage of the study.",{"count":279,"type":19},20,"This study aims to determine the potential for 'safe' and 'effective' use of Microsoft Xbox One-based motion games for the geriatric population through expert consensus using a unique set of assessments, and to provide clinicians with an evidence-based guide to game selection.",[28,260],[283,31,284,285],"exergame","Kinect sensory","security",{"date":266,"type":40},{"date":288,"type":19},"2026-04-30",{"date":269,"type":19},{"name":46,"class":47},{"id":292,"slug":293,"hasResults":11,"nctId":294,"briefTitle":295,"officialTitle":296,"acronym":4,"eligibilityCriteria":297,"healthyVolunteers":56,"sex":15,"minAge":119,"maxAge":4,"enrollmentInfo":298,"targetDuration":300,"studyType":122,"phases":4,"briefSummary":301,"conditions":302,"keywords":303,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":264,"lastUpdatePostDateStruct":307,"startDateStruct":308,"completionDateStruct":309,"leadSponsor":311,"locationsCount":84},"100636224","validity-and-reliability-of-the-exergame-enjoyment-questionnaire-eeq-in-turkish-100636224","NCT07562906","Validity and Reliability of the Exergame Enjoyment Questionnaire (EEQ) in Turkish","Validity and Reliability of the Exergame Enjoyment Questionnaire (EEQ) in a Geriatric Population in Turkish","Inclusion Criteria:\n\n* Being 65 years of age or older\n* Having participated in an exergaming application at least once before\n* Not having a physical, sensory or cognitive disability that would prevent participation in the exergaming application\n* Agreeing to participate voluntarily and providing informed consent\n\nExclusion Criteria:\n\n1. Individuals with active neurological, vestibular, or psychiatric disorders\n2. Individuals diagnosed with moderate or severe cognitive impairment (MMSE \\\u003C 24 and\u002For MoCA \\\u003C 21)\n3. Individuals with severe hearing or vision loss\n4. Individuals who are physically unable to participate in exergaming due to cardiopulmonary or orthopedic reasons\n5. Individuals with no prior exergaming experience\n6. Individuals who experience significant communication difficulties\n7. Participants who do not sign the voluntary consent form",{"count":299,"type":19},46,"2 Weeks","The aim of this research is to adapt the Exergame Enjoyment Questionnaire (EEQ) into Turkish and to evaluate its suitability for the Turkish elderly population through validity and reliability analyses. After the cultural adaptation process is completed, the construct validity of the scale will be evaluated using exploratory and confirmatory factor analyses; its reliability will be assessed through internal consistency coefficients (Cronbach's alpha) and test-retest reliability over time (ICC). Accordingly, the study aims to provide a valid and reliable assessment tool for clinicians and researchers who wish to evaluate individual experiences in exergaming-based interventions.",[28,125],[304,305,242,306],"exercise","exercise enjoyment","validation",{"date":266,"type":40},{"date":288,"type":19},{"date":310,"type":19},"2026-09-30",{"name":46,"class":47},{"id":313,"slug":314,"hasResults":11,"nctId":315,"briefTitle":316,"officialTitle":317,"acronym":318,"eligibilityCriteria":319,"healthyVolunteers":56,"sex":15,"minAge":119,"maxAge":4,"enrollmentInfo":320,"targetDuration":4,"studyType":122,"phases":4,"briefSummary":322,"conditions":323,"keywords":327,"overallStatus":101,"whyStopped":4,"lastUpdateSubmitDate":332,"lastUpdatePostDateStruct":333,"startDateStruct":335,"completionDateStruct":337,"leadSponsor":339,"locationsCount":84},"100624567","internal-jugular-vein-ultrasound-for-predicting-hypotension-in-geriatric-patients-undergoing-spinal-anesthesia-100624567","NCT07411313","Internal Jugular Vein Ultrasound for Predicting Hypotension in Geriatric Patients Undergoing Spinal Anesthesia","The Role of Internal Jugular Vein Ultrasonography in Predicting Hypotension in Geriatric Patients Undergoing Spinal Anesthesia: A Prospective Observational Study (Protocol ID: 2023-12\u002F509)","IJV-SPINAL","Inclusion Criteria:\n\n* Age ≥65 years\n* Scheduled to undergo surgery under spinal anesthesia\n* American Society of Anesthesiologists (ASA) physical status I-III\n* Able and willing to provide written informed consent\n\nExclusion Criteria:\n\n* Did not provide written informed consent\n* Undergoing emergency surgery\n* Body mass index (BMI) ≥40 kg\u002Fm²\n* Receiving angiotensin-converting enzyme (ACE) inhibitors\n* Pre-spinal systolic blood pressure \\\u003C90 mmHg or mean arterial pressure \\\u003C70 mmHg\n* Unable to tolerate the supine position\n* Left ventricular ejection fraction \\\u003C40%\n* Requiring sedoanalgesia in addition to spinal anesthesia or conversion to general anesthesia",{"count":321,"type":19},85,"Spinal anesthesia-induced hypotension is a common and clinically significant complication in geriatric patients. Accurate preoperative assessment of intravascular volume status may help identify patients at risk. Internal jugular vein (IJV) ultrasonography is a noninvasive and easily applicable bedside method that reflects venous volume status. This prospective observational study aims to evaluate the role of preoperative IJV ultrasonographic measurements in predicting hypotension following spinal anesthesia in geriatric patients. Patients aged 65 years and older undergoing elective surgery under spinal anesthesia will be included. Preoperative IJV diameter, cross-sectional area, and collapsibility index will be measured using ultrasonography. Hemodynamic parameters will be monitored intraoperatively, and the occurrence of hypotension after spinal anesthesia will be recorded. The predictive value of IJV ultrasonographic parameters for post-spinal hypotension will be analyzed",[324,28,325,326],"Spinal Anesthesia Induced Hypotension","Internal Jugular Vein","Ultrasonography",[328,329,330,326,331],"Geriatric patients","Spinal anesthesia","Hypotension","Internal jugular vein","2026-02-11",{"date":334,"type":40},"2026-02-13",{"date":336,"type":40},"2024-01-03",{"date":338,"type":19},"2026-02-10",{"name":340,"class":47},"Dr Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital",{"id":342,"slug":343,"hasResults":11,"nctId":344,"briefTitle":345,"officialTitle":346,"acronym":347,"eligibilityCriteria":348,"healthyVolunteers":11,"sex":15,"minAge":349,"maxAge":350,"enrollmentInfo":351,"targetDuration":4,"studyType":122,"phases":4,"briefSummary":353,"conditions":354,"keywords":361,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":363,"lastUpdatePostDateStruct":364,"startDateStruct":366,"completionDateStruct":367,"leadSponsor":369,"locationsCount":84},"100621551","complications-of-surgical-geriatrics-hospitalized-in-the-orinoco-region-100621551","NCT07372092","Complications of Surgical Geriatrics Hospitalized in the Orinoco Region","Surgical Geriatrics o Geriatric Surgery? Outcomes in a Novel Hospital Model of Attention. A Comparative Cohort Study.","SURGER","Inclusion Criteria:\n\n* Adults\n* Hospitalized in the surgical ward\n* Surgical procedures\n\nExclusion Criteria:\n\n* Derived to other institution\n* Operated previously in other institution","18 Years","100 Years",{"count":352,"type":19},150,"The life expectancy of the Colombian population is increasing. Older patients are frequently hospitalized and treated in surgical wards, and are treated as the general surgical population. However, geriatric patients are frequently found with additional comorbidities, besides the primary surgical diagnosis. Some diseases, like hip fractures, diverticulitis, and cancer, are common in this age range. The preoperative, intraoperative, and postoperative period requires a special care and planning to avoid complications related to the physical status, medications, and comorbidities. Studies about the geriatric surgical population are limited in the Orinoco region. The implementation of a comprehensive geriatric assesment in surgical services requires follow-up of outcomes.",[355,356,357,28,358,359,360],"Operative Surgical Procedures","Aged","Aged 65 Years or Older","Geriatric Assessment","Postoperative Care","Postoperative Complications",[355,356,362,358,359,360],"Geriatrics","2026-01-20",{"date":365,"type":40},"2026-01-28",{"date":137,"type":19},{"date":368,"type":19},"2027-12-31",{"name":370,"class":47},"Hospital Departamental de Villavicencio",{"id":372,"slug":373,"hasResults":11,"nctId":374,"briefTitle":375,"officialTitle":376,"acronym":377,"eligibilityCriteria":378,"healthyVolunteers":11,"sex":15,"minAge":4,"maxAge":4,"enrollmentInfo":379,"targetDuration":4,"studyType":122,"phases":4,"briefSummary":381,"conditions":382,"keywords":391,"overallStatus":101,"whyStopped":4,"lastUpdateSubmitDate":401,"lastUpdatePostDateStruct":402,"startDateStruct":404,"completionDateStruct":406,"leadSponsor":407,"locationsCount":409},"100616764","hip-fracture-surgery-timing-and-blood-transfusion-risk-in-patients-on-doacs-100616764","NCT07309848","Hip Fracture Surgery Timing and Blood Transfusion Risk in Patients on DOACs","Blood Transfusion Risk After Early vs. Delayed Surgery in Hip Fracture Patients on Direct Oral Anticoagulants: A Natural Experiment","OPTIMIZEDOAC","Inclusion Criteria:\n\n* Isolated hip fracture classified as AO\u002FOTA 31A or 31B requiring surgical intervention.\n* Current DOAC use with the last dose taken ≤24 hours before emergency department (ED) presentation\n\nExclusion Criteria:\n\n* Pathologic or periprosthetic hip fractures.\n* Fracture sustained \\>24 hours before ED presentation.\n* Inter-hospital transfer.\n* Hematologic disorders (e.g., thalassemia, sickle cell disease, aplastic anemia, myelodysplastic syndromes, leukemia).\n* Use of a non-EMA-approved DOAC (e.g., betrixaban).",{"count":380,"type":19},374,"This study looks at patients with hip fractures who are taking direct oral anticoagulants (DOACs), a type of blood thinner. In many hospitals, surgery for these patients is delayed because of concerns about bleeding, but waiting longer can also increase risks such as complications and longer hospital stays. The purpose of this study is to find out whether operating within 24 hours is as safe as delaying surgery beyond 24 hours. Specifically, the investigators want to know if early surgery does not lead to a higher need for blood transfusions compared to delayed surgery.",[383,384,28,385,386,387,388,389,390],"Blood Transfusion","Hip Fracture Surgeries","Bleeding Complications","Bleeding as Surgical Complication (Treatment)","Bleeding","Blood Transfusions","Blood Transfusion Complication","Direct Oral Anticoagulants (DOACs)",[392,393,394,395,31,396,397,398,399,400],"natural experiment","doac","direct oral anticoagulant","hip fracture","surgery","bleeding","blood transfusion","early","delayed","2025-12-15",{"date":403,"type":40},"2025-12-30",{"date":405,"type":40},"2025-11-01",{"date":368,"type":19},{"name":408,"class":47},"St. Antonius Hospital",7,{"id":411,"slug":412,"hasResults":11,"nctId":413,"briefTitle":414,"officialTitle":415,"acronym":416,"eligibilityCriteria":417,"healthyVolunteers":11,"sex":15,"minAge":349,"maxAge":4,"enrollmentInfo":418,"targetDuration":4,"studyType":122,"phases":4,"briefSummary":420,"conditions":421,"keywords":4,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":425,"lastUpdatePostDateStruct":426,"startDateStruct":428,"completionDateStruct":430,"leadSponsor":432,"locationsCount":84},"100603838","collection-of-digital-parameters-from-parts-of-the-neurological-examination-using-an-eye-tracker-100603838","NCT07141719","Collection of Digital Parameters From Parts of the Neurological Examination Using an Eye Tracker","A Digital Protocol for Neurological Examination Using Eye-Tracking","NEX-Eye","Inclusion Criteria:\n\n* ≥ 18 years of age.\n* Diagnosed or treated for a neurological disease.\n* Hospitalized or outpatient of the Department of Neurology, UKSH Campus Kiel.\n* Ability of the person to understand oral study information and study information sheet, and willingness to provide a signed and dated informed consent form.\n\nExclusion criteria:\n\n* Being under legal guardianship\n* Impaired decision-making capacity, or temporal or spatial disorientation which may be revealed within ordinary conversation or by a confirmed diagnosis of dementia. In case of doubt, the Montreal Cognitive Assessment (MoCA, pass cutoff score \\> 18 16) will be administered.",{"count":419,"type":19},600,"The neurological examination (NE) is a cornerstone of clinical neurology, with ocular motor assessment being a key component. Technology offers an opportunity to augment and standardize parts of the NE. Eye-tracking systems provide objective quantitative data on eye movements by continuously tracking the eye over time. This data can be used to derive parameters like saccadic latency, gaze velocity, and fixation stability with a precision that is impossible to achieve through human observation by neurologists. The integration of such technology could enhance the traditional NE.\n\nBefore such technology can be widely adopted, its feasibility and acceptability in a clinical population must be established. The primary purpose of this study is to assess the usability of a novel eye-tracking system from the patient's perspective when used in a clinical settings. A secondary purpose is to determine if quantitative data from the eye-tracker correlate with the findings of the traditional clinical neurological examination and to explore whether eye-tracking can provide additional, complementary information not typically captured by standard clinical assessment.\n\nTo achieve these aims, the study will assess several outcome measures. The primary outcome measure is the Usability of the Eye-Tracking System, which will be measured using the System Usability Scale (SUS).\n\nBeyond the primary objectives, this study will investigate two secondary objectives.\n\nThe first involves assessing the relationship between quantitative eye-tracking parameters and clinical ocular motor assessment. Specifically, the investigators will analyze objective, numerical data obtained from eye-tracking systems and the clinician's subjectively graded assessment of ocular movements derived from the standard neurological examination.\n\nThe second is the exploratory analysis of novel eye-tracking biomarkers. This involves quantifying and analyzing eye-tracking parameters not typically assessed during a routine NE. For example, the dynamics of the pupillary light reflex or the frequency of microsaccades. The aim is to identify potential digital biomarkers that could provide additional objective insights into ocular motor function and neurological status.",[28,422,423,424],"Parkinsons Disease (PD)","Progressive Supranuclear Palsy(PSP)","Neurological Diseases or Conditions","2025-08-24",{"date":427,"type":40},"2025-08-26",{"date":429,"type":19},"2025-08-31",{"date":431,"type":19},"2026-12-31",{"name":433,"class":47},"University of Kiel",{"id":435,"slug":436,"hasResults":11,"nctId":437,"briefTitle":438,"officialTitle":439,"acronym":4,"eligibilityCriteria":440,"healthyVolunteers":56,"sex":15,"minAge":349,"maxAge":441,"enrollmentInfo":442,"targetDuration":4,"studyType":20,"phases":444,"briefSummary":445,"conditions":446,"keywords":4,"overallStatus":101,"whyStopped":4,"lastUpdateSubmitDate":450,"lastUpdatePostDateStruct":451,"startDateStruct":453,"completionDateStruct":455,"leadSponsor":457,"locationsCount":84},"100527735","a-novel-multisensory-rhythmic-intervention-in-geriatric-rehabilitation-100527735","NCT06151626","A Novel Multisensory-Rhythmic Intervention in Geriatric Rehabilitation","Linking From an Artificial-Intelligence Driven Assessment of Upper Extremity Motor Adaptation to a Novel Multisensory-Rhythmic Intervention in Geriatric Rehabilitation","Inclusion Criteria:\n\n1. Montreal Cognitive Assessment (MoCA) score of 23 or higher,\n2. Clinical Dementia Rating (CDR) of 0 (for normal subjects) or 1 (for mild cognitive impairment subjects),\n3. Healthy young participants aged between 20-39 years, healthy older adults and mild cognitive impairment participants aged between 65-85 years,\n4. No skeletal, muscular, or neurological problems in the upper limbs in the past year, and\n5. Sufficient visual acuity to complete the tasks.\n\nExclusion Criteria:\n\n* Any subjects with significant mental illness, central nervous system disorders, or medical history","85 Years",{"count":443,"type":19},108,[22],"Human performance takes shape from the dynamic interaction between person, environment, and task. Goal-directed action is a complex task, which requires the elderly to adapt their motor response according to the environment constraints and task requirements to accomplish the task goal. Among age-related problems, motor control deficits are often the main problems which restricts the frail elderly from maintaining independence for activities of daily living. Therefore, to preserve the quality of life, motor function of the elderly must be taken into consideration, including early detection of motor control problems and development of appropriate intervention strategy for persons with either healthy or pathological brain aging. Rhythmic skill training which is a new mode of dual tasks using rhythmic cueing as an external agent for facilitating an automatized motor task. During training, rhythmic skill training can provide multi-component of sensory stimulation, strengthen motor planning and optimize motor execution, therefore, it will improve the motor performance for the elderly or patients with mild cognitive impairment. In addition, the neuroplastic changes related to sensory processing, selective attention, or working memory demands through music rhythm training can facilitate the cognitive function for the elderly which is a current trend of geriatric rehabilitation. Moreover, the advantage of virtual reality is that it provides important information related to knowledge of result, which can induce better motor and cognitive training effects. Therefore, this research project will focus on assessing and intervening motor adaptation of upper extremity for the healthy elderly and patients with mild cognitive impairment. The first purpose of the project will analyze the difference in efficiency of responsive and predictive grasping motor adaptation among the healthy young adults, healthy elderly and patients with mild cognitive impairment through a test of perturbation-based of pinch-holding-up-activity, and use artificial intelligence for more accurate classification for the grasp pattern of healthy young adults, elderly and patients with mild cognitive impairment. The second one is to verify the effects of virtual-reality based rhythmic skill training system on the motor adaptation capability of upper limb and cognition for the elderly and patients with mild cognitive impairment.",[447,448,28,449],"Virtual Reality","Hand Mirror","Kinesiology, Applied","2025-08-15",{"date":452,"type":40},"2025-08-21",{"date":454,"type":40},"2023-12-05",{"date":456,"type":19},"2026-12",{"name":458,"class":47},"National Cheng-Kung University Hospital",{"id":460,"slug":461,"hasResults":11,"nctId":462,"briefTitle":463,"officialTitle":464,"acronym":465,"eligibilityCriteria":466,"healthyVolunteers":11,"sex":15,"minAge":467,"maxAge":4,"enrollmentInfo":468,"targetDuration":4,"studyType":122,"phases":4,"briefSummary":469,"conditions":470,"keywords":473,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":479,"lastUpdatePostDateStruct":480,"startDateStruct":482,"completionDateStruct":484,"leadSponsor":486,"locationsCount":84},"100598554","three-month-follow-up-analysis-of-social-recommendations-issued-by-the-mobile-geriatric-team-100598554","NCT07073001","Three-month Follow-up Analysis of Social Recommendations Issued by the Mobile Geriatric Team","UMG-CHUSE Study: Three-month Follow-up Analysis of Social Recommendations Issued by the Mobile Geriatric Team.","UMG-CHUSE","Inclusion Criteria:\n\n* Patients aged 75 years or older\n* Patients assessed by the Mobile Geriatric Team of the Saint-Etienne University Hospital with the formulation of social recommendations\n* Patients residing at home or in a long-term care facility for dependent elderly individuals (nursing home \u002F EHPAD)\n* Informed consent obtained from the patient or their legal representative\n\nExclusion Criteria:\n\n* Patients under 75 years old\n* Refusal to participate in the study by the patient (or by the legally authorized representative\u002Ftrusted person).\n* Patients receiving exclusive palliative care\n* Inability to ensure follow-up: in case of non-response at three months or in the event of death","75 Years",{"count":93,"type":19},"This single-center, prospective, observational cohort study aims to evaluate the actual implementation rate of social recommendations formulated by the Mobile Geriatric Team at Saint-Étienne University Hospital three months after hospital discharge. These recommendations may include human assistance, technical aids, financial aid applications, legal protective measures, or referrals to appropriate care structures.\n\nA structured telephone interview at three months will assess the degree of implementation, explore associated barriers (administrative, cognitive, organizational, ...), and investigate any potential link with hospital readmissions or changes in patients' living situations.",[28,471,472],"Care Coordination","Readmission, Hospital",[362,474,475,476,477,478],"Mobile Geriatric Team","Care coordination","Social recommandations","Elderly care","Hospital readmission","2025-08-06",{"date":481,"type":40},"2025-08-11",{"date":483,"type":19},"2025-09",{"date":485,"type":19},"2026-01",{"name":487,"class":47},"Centre Hospitalier Universitaire de Saint Etienne",{"id":489,"slug":490,"hasResults":11,"nctId":491,"briefTitle":492,"officialTitle":492,"acronym":493,"eligibilityCriteria":494,"healthyVolunteers":11,"sex":15,"minAge":467,"maxAge":4,"enrollmentInfo":495,"targetDuration":4,"studyType":122,"phases":4,"briefSummary":497,"conditions":498,"keywords":499,"overallStatus":101,"whyStopped":4,"lastUpdateSubmitDate":502,"lastUpdatePostDateStruct":503,"startDateStruct":505,"completionDateStruct":507,"leadSponsor":509,"locationsCount":511},"100597258","association-between-early-consultation-by-the-primary-care-physician-after-hospitalization-in-geriatric-medicine-department-and-the-risk-of-re-hospitalization-at-1-and-3-months-100597258","NCT07056153","Association Between Early Consultation by the Primary Care Physician After Hospitalization in Geriatric Medicine Department, and the Risk of Re-hospitalization at 1 and 3 Months","GEREHOSP","Inclusion Criteria:\n\n1. Age ≥ 75 years\n2. Patients hospitalized in the geriatric department of one of the investigating centers\n3. Patient discharged home from the geriatrics department of one of the investigating centers\n4. No objection from patient or legal representative to participate in study\n\nExclusion Criteria:\n\n1. Patients who do not have a primary care physician\n2. Patients living in an institution or transferred to an institution",{"count":496,"type":19},301,"The time it takes for patients to be readmitted to hospital is a major public health issue, both in terms of medical time and costs.\n\nIn fact, 15% of patients of all ages are likely to be re-hospitalized within a month of hospitalization.\n\nToday, hospitalizations present a significant nosocomial risk, all the more so in fragile populations. If these hospitalizations are long or repeated, it is crucial to develop solutions to reduce their number.\n\nElderly people often have a number of complementary pathologies and frailties, which are frequently destabilized during hospitalization or on discharge.\n\nIn this context of medico-social and financial stakes, a 2012 survey showed that 86% of French physicians would be prepared to make themselves available within 24-48 hours of hospital discharge if the situation justified it. Changes in medical demographics are forcing primary care physicians to adapt their practices, and the evidence of a reduced risk of re-hospitalization would make it possible to prioritize the provision of this consultation on discharge from hospital.\n\nPost-hospitalization follow-up consultations with the primary care physician are recommended, but investigators have very little data on their benefits.\n\nInvestigators hypothesise that an early consultation (1 month post-hospitalization at most) by an elderly patient's primary care physician after hospitalization in geriatric medicine promotes: patient follow-up; reduced risk of re-hospitalization within 3 months.\n\nThe aim of this study is to determine the association of an early consultation by the primary care physician in the month following discharge from geriatric medicine hospitalization with rehospitalization rates within 3 months.",[28],[500,501],"primary care physician","early post-hospitalization consultation","2025-07-10",{"date":504,"type":40},"2025-07-15",{"date":506,"type":40},"2025-06-19",{"date":508,"type":19},"2026-03",{"name":510,"class":47},"Groupe Hospitalier Mutualiste de Grenoble",3,{"id":513,"slug":514,"hasResults":11,"nctId":515,"briefTitle":516,"officialTitle":516,"acronym":4,"eligibilityCriteria":517,"healthyVolunteers":56,"sex":15,"minAge":119,"maxAge":4,"enrollmentInfo":518,"targetDuration":4,"studyType":122,"phases":4,"briefSummary":519,"conditions":520,"keywords":4,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":523,"lastUpdatePostDateStruct":524,"startDateStruct":526,"completionDateStruct":528,"leadSponsor":529,"locationsCount":4},"100592528","investigation-of-respiratory-muscle-sarcopenia-in-geriatric-individuals-100592528","NCT06994598","Investigation of Respiratory Muscle Sarcopenia in Geriatric Individuals","Inclusion Criteria:\n\n* Being 65 years of age or older.\n* Being clinically stable\n* Being able to adapt to tests (visual, cognitive, cooperative)\n\nExclusion Criteria:\n\n* Those with neurological and\u002For musculoskeletal problems that may affect the study\n* Presence of severe joint contracture or painful ulcers that may affect muscle strength measurement and walking\n* Presence of serious infection or sepsis\n* Having a known additional rheumatologic disease diagnosis\n* Any stage of cancer",{"count":321,"type":19},"The increase in the elderly population worldwide necessitates further research on age-related physiological changes and health problems related to these changes in geriatric individuals. One of these problems, sarcopenia, is a syndrome characterized by a decrease in muscle mass, muscle strength, and physical performance due to aging (Cruz-Jentoft et al., 2019). Sarcopenia affects not only the extremity muscles but also the respiratory muscles, significantly reducing the individual's functional capacity and quality of life (Shafiee et al., 2017). Sarcopenia is a progressive and widespread loss of skeletal muscles, characterized by a decrease in muscle strength, muscle mass, and physical performance. Although it is usually seen in older individuals, it can also occur in people with certain diseases or who lead a sedentary lifestyle. The European Working Group on Sarcopenia in Older People (EWGSOP) has developed a guideline for the diagnosis of sarcopenia and determination of its severity (Cruz-Jentoft et al., 2019). In line with this guideline, the EWGSOP considers sarcopenia in three basic stages: pre-sarcopenia, sarcopenia, and severe sarcopenia (Cruz-Jentoft et al., 2010). Pre-sarcopenia is the stage in which muscle mass is low but muscle strength or physical performance is not yet affected. Sarcopenia is the stage in which low muscle mass is accompanied by decreased muscle strength or low physical performance. Severe sarcopenia is defined as the most advanced stage in which all these criteria are met (Cruz-Jentoft et al., 2010). Respiratory muscle sarcopenia is defined as muscle fiber atrophy and weakness in the respiratory muscles. The Japanese Respiratory Sarcopenia Study Group defines this condition as whole-body sarcopenia with low respiratory muscle mass, decreased respiratory muscle strength, and\u002For respiratory dysfunction (Nagano et al., 2021). Kera et al. (2019) evaluated respiratory muscle sarcopenia according to the peak expiratory flow rate value. However, whole-body sarcopenia and respiratory muscle strength are considered important parameters in the definition and diagnosis of respiratory muscle sarcopenia. It is reported that the rate of respiratory muscle sarcopenia is higher in the presence of sarcopenia (Nagano et al., 2021). Sarcopenic respiratory failure is diagnosed in the presence of sarcopenia accompanied by functional disability, while individuals without functional disability but at risk for respiratory muscle sarcopenia are considered \"at risk of sarcopenic respiratory failure\" (Nagano et al., 2021). Sarcopenia is thought to be associated with insulin resistance and oxidative stress, leading to decreased muscle strength and muscle mass, as well as muscle atrophy (Ding et al., 2019). Respiratory muscles may also be affected in a similar way. Thus, weakening of respiratory muscles may lead to decreased respiratory function and decreased quality of life. In the current literature, studies examining the effects of aging on respiratory muscles are limited. Therefore, determining the potential effects of aging on respiratory muscles and evaluating respiratory muscle sarcopenia in this context may provide an important contribution to the development of new approaches and the literature.",[28,521,522],"Sarcopenia","Diaphragm","2025-05-20",{"date":525,"type":40},"2025-05-29",{"date":527,"type":19},"2025-05",{"date":483,"type":19},{"name":530,"class":47},"Kirsehir Ahi Evran Universitesi",{"id":532,"slug":533,"hasResults":11,"nctId":534,"briefTitle":535,"officialTitle":536,"acronym":4,"eligibilityCriteria":537,"healthyVolunteers":56,"sex":15,"minAge":119,"maxAge":4,"enrollmentInfo":538,"targetDuration":4,"studyType":20,"phases":540,"briefSummary":541,"conditions":542,"keywords":4,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":546,"lastUpdatePostDateStruct":547,"startDateStruct":548,"completionDateStruct":550,"leadSponsor":552,"locationsCount":4},"100591429","comparing-music-supported-and-traditional-aerobic-training-in-geriatric-health-outcomes-100591429","NCT06980311","Comparing Music-Supported and Traditional Aerobic Training in Geriatric Health Outcomes","Comparison of the Effects of Music Therapy-Based Aerobic Exercise and Traditional Aerobic Exercise Training on Cardiopulmonary Functions, Functional Capacity, Balance, Peripheral Muscle Strength, Cognitive Functions, Depression, and Quality of Life in Geriatrics","Inclusion Criteria:\n\n* Being 65 years of age or older\n* Willingness to participate in the study\n\nExclusion Criteria:\n\n* Presence of uncontrolled hypertension (≥180\u002F110 mmHg) or severe complications of diabetes (e.g., diabetic neuropathy, proliferative retinopathy, uncontrolled hypoglycemic episodes)\n* Presence of respiratory diseases such as Chronic Obstructive Pulmonary Disease (COPD), asthma, etc.\n* Presence of chronic neurological disorders such as Multiple Sclerosis (MS), Parkinson's Disease, Amyotrophic Lateral Sclerosis (ALS), etc.\n* Diagnosis of any oncological disease\n* Presence of acute musculoskeletal conditions that would prevent participation in exercise (e.g., fracture, advanced osteoarthritis, severe musculoskeletal injuries)\n* Having undergone any surgical operation within the past 6 months\n* Presence of visual or auditory impairments that could interfere with the assessment procedures\n* A score of ≤24 on the Mini-Mental State Examination (MMSE), indicating cognitive impairment\n* Participation in a regular exercise program within the last six months",{"count":539,"type":19},33,[22],"The aim of this study is to comparatively evaluate the effects of a music therapy-based aerobic exercise program and traditional aerobic exercise training on cardiopulmonary functions, functional capacity, balance, peripheral muscle strength, cognitive functions, depression level and quality of life in geriatric individuals.",[28,543,544,545],"Aerobic Exercise","Music Therapy","Physiotherapy and Rehabilitation","2025-05-17",{"date":523,"type":40},{"date":549,"type":19},"2025-06-01",{"date":551,"type":19},"2027-06-01",{"name":553,"class":47},"Bezmialem Vakif University",{"id":555,"slug":556,"hasResults":11,"nctId":557,"briefTitle":558,"officialTitle":559,"acronym":4,"eligibilityCriteria":560,"healthyVolunteers":11,"sex":15,"minAge":119,"maxAge":4,"enrollmentInfo":561,"targetDuration":4,"studyType":20,"phases":563,"briefSummary":564,"conditions":565,"keywords":573,"overallStatus":101,"whyStopped":4,"lastUpdateSubmitDate":578,"lastUpdatePostDateStruct":579,"startDateStruct":581,"completionDateStruct":583,"leadSponsor":585,"locationsCount":84},"100585459","geriatric-trauma-care-program-for-living-alone-older-adults-with-injuries-100585459","NCT06902636","Geriatric Trauma Care Program for Living Alone Older Adults With Injuries","Patient Experience of Older Adults Living Alone With Injuries and Long-Term Effects of Geriatric Trauma Care Program for Living Alone Older Adults With Injuries","Inclusion Criteria:\n\n1. willing to join this study for three months\n2. with limb injuries\n3. living alone in a household\n4. aged 65 years old or older\n5. independent before a traumatic injury\n6. having a smartphone.\n\nExclusion Criteria:\n\n1. with an ISS greater than 16 (severe injuries)\n2. having cognitive impairments\n3. diagnosed with psychiatric illness",{"count":562,"type":19},90,[22],"To examine the long-term effects of the Geriatric Trauma Care Program (GTCP) regarding pain, functional disability, depression, loneliness, and health-related quality of life among older adults with traumatic injuries who live alone.",[566,567,28,568,569,570,571,572],"Limb Injury","Older Adults","Pain","Geriatric Depression","Barthel Index","Quality of Life","Loneliness",[574,575,576,577],"Limb injury","geriatric trauma","older adults","loneliness","2025-05-13",{"date":580,"type":40},"2025-05-16",{"date":582,"type":40},"2025-03-27",{"date":584,"type":19},"2026-07-31",{"name":586,"class":47},"Kaohsiung Medical University",{"id":588,"slug":589,"hasResults":11,"nctId":590,"briefTitle":591,"officialTitle":592,"acronym":593,"eligibilityCriteria":594,"healthyVolunteers":11,"sex":15,"minAge":119,"maxAge":4,"enrollmentInfo":595,"targetDuration":4,"studyType":122,"phases":4,"briefSummary":597,"conditions":598,"keywords":601,"overallStatus":101,"whyStopped":4,"lastUpdateSubmitDate":607,"lastUpdatePostDateStruct":608,"startDateStruct":610,"completionDateStruct":611,"leadSponsor":613,"locationsCount":84},"100588832","nutritional-status-and-patient-characteristics-upon-length-of-stay-clinical-outcome-and-survival-in-older-hospitalized-patients-100588832","NCT06946537","Nutritional Status and Patient Characteristics Upon Length of Stay, Clinical Outcome, and Survival in Older Hospitalized Patients","The Influence of Nutritional Status and Phenotypic Characteristics Upon Length of Stay, Clinical Outcome, and Survival in Hospitalized Patients","INSIGHT","Inclusion Criteria:\n\n* Acutely admitted adults aged 65 years and above.\n* Be able to comply with the study information, as assessed by the research personnel.\n* Be able to understand Danish.\n\nExclusion Criteria:\n\n* \\\u003C24 hours admission\n* Terminal illness in end stage of life\n* Patients with temporary civil person registration number (CPR)",{"count":596,"type":19},1500,"Disease-related malnutrition (DRM) describes undernutrition or imbalances in energy, protein, or other nutrient-needs, caused by a concomitant disease. Nutritional status plays a vital role in the fate of hospitalized patients, and DRM is associated with loss of function and decreased survival.\n\nDRM is a common condition in patients with acute illnesses, approximately 30% among medical inpatients are malnourished when admitteed to the hospital, and rise higher among the older or critically ill. Physiologically malnutrition is associated with a) poorer tissue healing and restitution after severe disease, b) suppressed immune function and resistance towards infections, c) poorer metabolic defense towards critical disease, d) delayed and poorer progress of chronic diseases. In addition, inadequate nutrition is coupled to a prolonged hospital stay, resulting in more readmissions, and overall higher mortality in hospital patients. Yet, nutritional status of patients upon hospital admittance is seldom systematically assessed and the consequences of DRM in older acutely admitted patients still needs to be understood.\n\nThis project will provide a detailed description of nutritional, physiolgical, and biochemical status of 1500 acutely admitted patients. In relation, the study will investigate the relation between patient characteristics and disease progression. The obtained data will also be coupled to patient registers to investigate the link between length of hospital stay, readmissions and acute contact, and mortality.",[28,599,600],"Malnutrition","Length of Stay",[28,602,603,604,605,606],"Disease-related malnutrition","Physiology","Acute illness","Deep phenotyping","Nutritional status","2025-05-12",{"date":609,"type":40},"2025-05-14",{"date":607,"type":40},{"date":612,"type":19},"2028-11",{"name":614,"class":47},"Bispebjerg Hospital",{"id":616,"slug":617,"hasResults":11,"nctId":618,"briefTitle":619,"officialTitle":619,"acronym":620,"eligibilityCriteria":621,"healthyVolunteers":11,"sex":15,"minAge":119,"maxAge":4,"enrollmentInfo":622,"targetDuration":4,"studyType":20,"phases":623,"briefSummary":624,"conditions":625,"keywords":4,"overallStatus":101,"whyStopped":4,"lastUpdateSubmitDate":643,"lastUpdatePostDateStruct":644,"startDateStruct":646,"completionDateStruct":648,"leadSponsor":650,"locationsCount":652},"100493872","the-save-project-sarcopenia-and-vertigo-in-aging-patients-with-colorectal-cancer-100493872","NCT05710809","The SaVe Project-Sarcopenia and Vertigo in Aging Patients With Colorectal Cancer","SaVe","Inclusion Criteria:\n\n* Meet the criteria of the oncological departments of receiving neoadjuvant, adjuvant or first line palliative chemotherapy for colorectal cancer\n* ≥65 years of age at the time of signing the informed consent form\n* Able to speak and read Danish, and to provide a signed informed consent form\n* Have an Eastern Cooperative Oncology Group (ECOG) performance status score of ≤2\n\nExclusion Criteria:\n\n* Chemotherapy treatment within two years and sequelae of neuropathy, or symptoms of dizziness or vertigo, or balance disturbance\n* Severe physical disability that hinders physical exercise\n* Dementia, psychotic disorders, or other cognitive diseases or conditions that hinder participation in a clinical exercise-based trial\n* Inability to sign informed content\n* Patients who have had a consultation in the geriatric outpatient clinic within the past six months",{"count":352,"type":19},[22],"The goal of this clinical trial is to learn about the cause of dizziness and decline in walking ability in in older adults ≥65 years during chemotherapy treatment for colorectal cancer. Another goal is to investigate if a comprehensive geriatric assessment and three months' specialized physical group-based exercise three times\u002Fweek can counteract muscle weakness, vertigo, instability, impaired walking balance, and neuropathy",[626,627,628,629,630,521,631,632,63,633,28,125,634,567,635,636,637,638,639,640,641,642],"Colorectal Cancer","Oncologic Complications","Comprehensive Geriatric Assessment","Vestibular Rehabilitation","Geriatric Oncology","Vertigo","Cancer","Exercise","Frail","Chemotherapy","Chemotherapy-induced Peripheral Neuropathy","Resistance Training","Balance Training","Postural Stability","Pragmatic Trial","Personal Medicine","Individualised","2025-04-02",{"date":645,"type":40},"2025-04-06",{"date":647,"type":40},"2023-02-20",{"date":649,"type":19},"2027-09",{"name":651,"class":47},"Rigshospitalet, Denmark",2,{"id":654,"slug":655,"hasResults":11,"nctId":656,"briefTitle":657,"officialTitle":658,"acronym":659,"eligibilityCriteria":660,"healthyVolunteers":56,"sex":15,"minAge":119,"maxAge":4,"enrollmentInfo":661,"targetDuration":4,"studyType":122,"phases":4,"briefSummary":663,"conditions":664,"keywords":4,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":670,"lastUpdatePostDateStruct":671,"startDateStruct":673,"completionDateStruct":675,"leadSponsor":677,"locationsCount":4},"100586133","palliative-assessment-cohort-in-the-geriatric-emergency-setting-100586133","NCT06911411","PALLIATIVE ASSESSMENT COHORT IN THE GERIATRIC EMERGENCY SETTING","PALLIATIVE ASSESSMENT AND MANAGEMENT IN THE GERIATRIC EMERGENCY SETTING (PALMA)","PALMA cohort","Inclusion Criteria: Older patient \\>64 years acutely admitted to the geriatric emergency department -\n\nExclusion Criteria: Severe cognitive impairment. Not able to provide informed consent. Not reading Danish\n\n\\-",{"count":662,"type":19},300,"The PALMA project is part of a larger palliative research program COPAL in Capital Region of Denmark led by Professor Tom Møller. PALMA aims to improve palliative care for geriatric patients transitioning from emergency-hospital to primary care. The project addresses the lack of a systematic approach for assessing and managing palliative symptoms in geriatric patients to enhance communication between hospitals and municipal health care services.\n\nThe PALMA cohort investigates the applicability of systematic palliative assessment (EORTC-C15 PAL) in the geriatric emergency setting combined with measures of frailty, socio-demographic risks, and cross-sectoral healthcare support.",[28,665,666,667,572,668,669],"Palliative Care","Socio-demographic Risk","Frailty at Older Adults","Collaborative Care","Transition of Care","2025-03-28",{"date":672,"type":40},"2025-04-04",{"date":674,"type":19},"2025-04-01",{"date":676,"type":19},"2026-12-30",{"name":678,"class":47},"University Hospital Bispebjerg and Frederiksberg",{"id":680,"slug":681,"hasResults":11,"nctId":682,"briefTitle":683,"officialTitle":684,"acronym":4,"eligibilityCriteria":685,"healthyVolunteers":11,"sex":15,"minAge":119,"maxAge":4,"enrollmentInfo":686,"targetDuration":4,"studyType":122,"phases":4,"briefSummary":688,"conditions":689,"keywords":693,"overallStatus":101,"whyStopped":4,"lastUpdateSubmitDate":699,"lastUpdatePostDateStruct":700,"startDateStruct":702,"completionDateStruct":704,"leadSponsor":705,"locationsCount":84},"100576345","relationship-between-fracture-type-and-preoperative-nutritional-status-with-postoperative-pain-100576345","NCT06784089","Relationship Between Fracture Type and Preoperative Nutritional Status with Postoperative Pain","Relationship Between Fracture Type and Preoperative Nutritional Status with Postoperative Pain and Prognosis in Geriatric Hip Surgery","Inclusion Criteria:\n\n* Patients undergoing hip surgery\n* Patients with informed consent\n* Patients over the age of 65\n* Patients undergoing surgery with spinal anesthesia\n* Patients evaluated in the ASA (American Society of Anesthesiologist) 1-2-3 category\n* Those with a body mass index (BMI) between 18-35\n\nExclusion Criteria:\n\n* Patients with ASA 4 and above\n* Patients under the age of 65\n* Those with a BMI below 18 and above 35,\n* Patients with systemic inflammatory diseases,\n* Patients using continuous anti-inflammatory\u002Fanalgesic drugs,\n* Patients with chronic pain before surgery,\n* Those with pathological fractures,\n* Multiple traumas\n* Those with end-stage disease (malignancy),\n* Severe renal failure, gastrointestinal ulceration or severe asthma that prevents the use of standard analgesia protocol\n* Patients who have previously had hip surgery on the same side\n* Patients who want to have surgery with general anesthesia\n* Patients who need general anesthesia in addition to spinal anesthesia\n* Those with a history of Pulmonary Thromboembolism",{"count":687,"type":19},95,"The geriatric patient group is a population that should be considered differently than other age groups due to physiological characteristics that change with age. When literature data is examined, it is seen that patients over the age of 65 are evaluated differently in studies. The rapid aging of the general population causes more elderly patients to need surgery. However, malnutrition is a common comorbidity in surgical patients . In addition, chronic diseases, multiple drug addiction, low nutritional intake, decreased appetite and psychological conditions seen in geriatric patients are risk factors for the development of nutritional deficiencies . Therefore, it is important to specifically consider geriatric patients, who frequently have these risk factors, in terms of malnutrition and to evaluate the nutritional status of these patients before surgery. It is estimated that the prevalence of malnutrition in hospitalized geriatric patients varies between 30% and 60%, depending on the population studied and the assessment tools applied . Despite these high malnutrition rates, this issue has not received sufficient clinical attention. Furthermore, malnutrition is highly associated with the prognosis of elderly perioperative patients, which may lead to poor clinical outcomes, increased morbidity and mortality, complication rates, decreased quality of life, prolonged hospital stay, and increased hospital and healthcare costs. A number of different screening tools are currently available to assess nutritional status in the elderly. However, there is currently no gold standard. The Nutrition Risk Score 2002 (NRS2002) is a nutritional screening tool for adult inpatients, launched in 2002 by the European Society of Clinical Nutrition and Metabolism (ESPEN). The Mini Nutritional Assessment - Short Form (MNA-SF), recommended by the European Union, and the Geriatric Nutrition Risk Index (GNRI), which has recently been evaluated as a new screening tool, has been validated for the diagnosis of malnutrition and the prediction of clinical outcomes, and is based on objective measurements that do not require patient cooperation, and whose validity has been demonstrated in other studies for the prediction of short- and long-term outcomes. In addition, the Prognostic Nutrition Index (PNI) is an indicator used to assess the nutritional status of surgical patients, estimate the risk of surgery, and make prognostic judgments. Although it has been stated that all four nutritional screening tools mentioned above can be used as prognostic indicators in geriatric surgical patients, the relationship between these screening tools and postoperative pain, complications, and hospital stay in geriatric patients undergoing orthopedic hip surgery has not yet been evaluated.\n\nHip fracture is a painful event that is frequently seen in older adults. Hip fractures are generally classified as femoral head fracture, femoral neck fracture, intertrochanteric fracture, and subtrochanteric fracture. Hip fracture is treated with proximal femoral nailing, partial hip replacement, and total hip replacement surgeries. Studies have reported that patients experience very high rates of moderate to severe pain following hip fracture surgery. This situation shows that the approach to pain management in hip surgery is still inadequate and that investigators need different perspectives on postoperative pain in these patients. It is known that hip fracture is associated with serious morbidity, mortality, and disability in the elderly. Inadequate pain management in these patients is associated with low motivation and has a high impact on functional recovery. Therefore, adequate pain management is important in patients with hip fractures to prevent mental and physical complications and to ensure appropriate compliance with rehabilitation. It is known that pain is affected by many factors such as biophysiological, biochemical, demographic, psychosocial, behavioral and moral variables and age. It is known that unmanaged postoperative pain will significantly affect cardiopulmonary and thromboembolic complications, morbidity and mortality, hospital discharge, quality of life and daily activities. In this context, determining the factors that predict acute pain will allow earlier intervention. Thus, short- and long-term morbidity, medication use, hospital stay and, accordingly, healthcare expenses will be reduced.This study aimed to evaluate the relationship between preoperative hip fracture type, surgery type, nutritional status and postoperative pain and prognosis (complications and hospital stay) in geriatric patients who will undergo hip surgery due to hip fracture. Secondly, it was aimed to determine which of the above-mentioned nutritional risk screening tools would be more appropriate in these patients and which nutritional risk screening tool could predict postoperative pain and prognosis in patients who will undergo hip surgery.",[690,691,692,28],"Nutrition","Postoperative Pain","Hip Fracture",[694,695,696,697,698],"nutritional status","hip surgery.","geriatric patients","postoperative pain","postoperative prognosis","2025-02-11",{"date":701,"type":40},"2025-02-12",{"date":703,"type":40},"2025-01-15",{"date":403,"type":19},{"name":706,"class":172},"Ankara Ataturk Sanatorium Training and Research Hospital"]