[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Bartın Unıversity\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":303},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,10,0,[8,48,79,119,145,174,204,226,253,276],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":30,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":4},"100631901","digital-education-for-hypertension-management-effects-on-self-care-and-health-literacy-100631901",false,"NCT07506707","Digital Education for Hypertension Management: Effects on Self-Care and Health Literacy","Digital Education Approach in Hypertension Management: Its Effect on Self-Care Behaviors and Health Literacy","DIGIHYPE-HTN","Inclusion Criteria:\n\n* Adults aged 50 years or older\n* Individuals with a clinical diagnosis of hypertension or those regularly using antihypertensive medication\n* Individuals actively registered at the Life Center and receiving regular services\n* Participants who provide written and verbal informed consent to voluntarily join the study\n* Individuals able to fully participate in the designated digital health education sessions\n* Participants capable of maintaining consistency throughout the intervention and follow up periods\n\nExclusion Criteria:\n\n* Individuals without a diagnosis of hypertension\n* Individuals unable to complete questionnaires or education sessions due to communication barriers or cognitive limitations\n* Illiterate individuals, as data collection requires reading and completing written questionnaires\n* Individuals unable to maintain participation or adhere to the follow up schedule during the study period","ALL","50 Years","80 Years",{"count":21,"type":22},166,"ESTIMATED","INTERVENTIONAL",[25],"NA","The goal of this clinical trial is to learn whether a digital education program can help people with high blood pressure (hypertension) manage their condition better. The program aims to improve self-care behaviors and health literacy by teaching participants how to use digital tools, follow healthy lifestyle habits, and take their medicines regularly.\n\nResearchers will compare two groups. One group will receive digital education that includes short videos, brochures, and podcasts about blood pressure control and how to use online health platforms such as e-Nabız (Turkey's national e-health system). The other group will not receive this education. Participants will attend two sessions during two weeks.\n\nThe main questions are:\n\nDoes digital education improve self-care and e-health literacy in people with hypertension? Does it help participants take their medicine as prescribed and maintain healthy habits such as diet and exercise?",[28,29],"Hypertension","High Blood Pressure",[28,31,32,33,34,35],"Digital education","Self-care behaviors","Health literacy","e-Health literacy","Medication adherence","NOT_YET_RECRUITING","2026-04-03",{"date":39,"type":40},"2026-04-08","ACTUAL",{"date":42,"type":22},"2026-04-11",{"date":44,"type":22},"2026-05-30",{"name":46,"class":47},"Bartın Unıversity","OTHER",{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":54,"eligibilityCriteria":55,"healthyVolunteers":56,"sex":57,"minAge":58,"maxAge":19,"enrollmentInfo":59,"targetDuration":4,"studyType":23,"phases":61,"briefSummary":62,"conditions":63,"keywords":65,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":70,"lastUpdatePostDateStruct":71,"startDateStruct":73,"completionDateStruct":75,"leadSponsor":77,"locationsCount":78},"100630315","osteoporosis-education-and-its-impact-on-osteoporosis-health-beliefs-and-awareness-in-women-at-risk-of-osteoporosis-100630315","NCT07486076","OSTEOPOROSIS EDUCATION AND ITS IMPACT ON OSTEOPOROSIS HEALTH BELIEFS AND AWARENESS IN WOMEN AT RISK OF OSTEOPOROSIS","THE EFFECT OF A HEALTH BELIEF MODEL-BASED EDUCATION PROGRAMME ON OSTEOPOROSIS AWARENESS AND HEALTH BELIEFS IN WOMAN AT RISK OF OSTEOPOROSIS: A RANDOMISED CONTROLLED TRIAL","HBM-osteo-edu","Inclusion Criteria:\n\n* Inclusion Criteria: Individuals meeting the following criteria will be included in the study:\n\n  * Being a woman aged 45 and over\n  * Not having been diagnosed with osteoporosis\n  * Having at least one of the risk factors for osteoporosis development as stated in the literature (being in menopause, family history of osteoporosis, low level of physical activity, insufficient calcium\u002Fvitamin D intake, low body mass index, etc.)\n  * Having applied to the Physical Therapy and Rehabilitation Outpatient Clinic of Bartın State Hospital\n  * Volunteering to participate in the study and signing the informed consent form\n  * Having the cognitive and physical capacity to participate in the training sessions\n\nExclusion Criteria:Exclusion Criteria: Individuals with the following characteristics will be excluded from the study:\n\n* Having a previous diagnosis of osteoporosis\n* Having a serious endocrine or rheumatological disease affecting bone metabolism\n* Having a history of long-term (≥ 3 months) systemic corticosteroid use\n* Having participated in a structured education program related to osteoporosis within the last 6 months\n* Having hearing, vision, or cognitive impairment that would prevent participation in the education program\n* Wishing to withdraw from the study or being unable to complete the follow-up process-",true,"FEMALE","45 Years",{"count":60,"type":22},74,[25],"Osteoporosis is a significant public health problem characterized by low bone mass and deterioration in the microarchitecture of bone tissue, leading to an increased risk of fractures. Risk factors such as advanced age, female gender, inadequate calcium and vitamin D intake, physical inactivity, smoking, and alcohol use play a critical role in its development. As in many countries, the prevalence of osteoporosis is increasing in Turkey, accelerated by an aging population and lifestyle changes. However, it is reported that the level of awareness and knowledge about osteoporosis in the community is often insufficient.\n\nThis study is a randomized controlled experimental trial with a two-group pretest-posttest design, conducted between February 1 and June 1, 2026, among women aged 45 and older who have not been diagnosed with osteoporosis but carry at least one osteoporosis risk factor, attending the Physical Therapy and Rehabilitation outpatient clinic at Bartın State Hospital. From the study population, participants who meet the inclusion criteria and volunteer will be randomly assigned to intervention and control groups. The sample size is determined as 74, calculated with a 95% confidence level and a 5% margin of error. While the intervention group receives a structured education program based on the Health Belief Model, the control group will receive no education.\n\nThe dependent variables of the study are osteoporosis awareness and health beliefs. These variables will be measured before and after the intervention using the Osteoporosis Awareness Scale and the Osteoporosis Health Belief Scale, which includes subdimensions of perceived susceptibility, seriousness, benefits, and barriers. The effectiveness of the education program will be evaluated through inter-group and intra-group comparisons.",[64],"Health Belief Model-Based Osteoporosis Education Programme",[66,67,68,69],"Health Belief Model-Based Education","Osteoporosis Awareness","Health Beliefs in Woman","Osteoporosis risk","2026-03-28",{"date":72,"type":40},"2026-04-02",{"date":74,"type":22},"2026-04-25",{"date":76,"type":22},"2026-12-20",{"name":46,"class":47},1,{"id":80,"slug":81,"hasResults":11,"nctId":82,"briefTitle":83,"officialTitle":84,"acronym":4,"eligibilityCriteria":85,"healthyVolunteers":56,"sex":17,"minAge":86,"maxAge":4,"enrollmentInfo":87,"targetDuration":4,"studyType":23,"phases":89,"briefSummary":90,"conditions":91,"keywords":105,"overallStatus":110,"whyStopped":4,"lastUpdateSubmitDate":111,"lastUpdatePostDateStruct":112,"startDateStruct":114,"completionDateStruct":116,"leadSponsor":118,"locationsCount":78},"100624078","the-effect-of-surgical-mask-and-n95-mask-use-on-surgical-smoke-in-operating-room-nurses-100624078","NCT07404956","THE EFFECT OF SURGICAL MASK AND N95 MASK USE ON SURGICAL SMOKE IN OPERATING ROOM NURSES","COMPARISON OF THE EFFECTS OF SURGICAL MASK AND N95 MASK USE ON PHYSICAL SYMPTOMS OF SURGICAL SMOKE IN OPERATING ROOM","Inclusion Criteria:\n\n* Willingness to participate in the study\n* Aged 18 years or older\n* Working as a sterile operating room nurse at least 4 hours per day, 5 days per week\n* Compliance with the protocol requiring continuous use of both surgical mask and N95 mask for at least 4 hours per day\n* Ability to communicate verbally and provide informed consent\n\nExclusion Criteria:\n\n* Diagnosed psychiatric disorders\n* Presence of chronic respiratory, musculoskeletal, or neurological diseases\n* Presence of chronic dermatological conditions or allergies affecting the facial or respiratory area\n* Speech or communication impairments\n* Pregnancy\n* Holding a supervisory role (e.g., charge nurse) or non-sterile nursing role\n* Planned unit change or rotation during the study period","18 Years",{"count":88,"type":22},38,[25],"This study was conducted to compare the effect of surgical mask and N95 mask use on physical symptoms due to surgical smoke in operating theatre nurses. The study, which was conducted in a single-group prospective quasi-experimental design, was completed with 38 nurses in the operating theatre unit of a state hospital in the Western Black Sea Region. Data were collected for four weeks using the Descriptive Information Form, Numerical Rating Scale and Symptom Follow-up Form. According to the findings, muscle weakness, myalgia in the upper extremities and muscle cramps were statistically significantly less in nurses using N95 masks. Respiratory parameters, watery eyes and redness were significantly lower in nurses using surgical masks. As a result, it was determined that the type of mask was effective on the incidence of physical symptoms related to surgical smoke.",[92,93,94,95,96,97,98,99,100,101,102,103,104],"Surgical Smoke Exposure","Occupational Exposure to Surgical Smoke","Headache","Dizziness","Nause and Vomiting","Fatigue Symptom","Eye Allergies","Abdominal Pain (AP)","Heart Rate Determination","SpO2","Muscle Weakness | Patient","Muscle Aches","Dispnea",[106,107,108,109],"Surgical Smoke","Masks","Operating Room Nurses","Occupational Exposure","RECRUITING","2026-02-09",{"date":113,"type":40},"2026-02-12",{"date":115,"type":40},"2024-09-15",{"date":117,"type":22},"2026-02-28",{"name":46,"class":47},{"id":120,"slug":121,"hasResults":11,"nctId":122,"briefTitle":123,"officialTitle":124,"acronym":4,"eligibilityCriteria":125,"healthyVolunteers":56,"sex":17,"minAge":86,"maxAge":4,"enrollmentInfo":126,"targetDuration":4,"studyType":23,"phases":128,"briefSummary":129,"conditions":130,"keywords":133,"overallStatus":110,"whyStopped":4,"lastUpdateSubmitDate":137,"lastUpdatePostDateStruct":138,"startDateStruct":140,"completionDateStruct":142,"leadSponsor":144,"locationsCount":78},"100620201","effects-of-different-relaxation-therapies-on-pain-and-sleep-in-hip-and-knee-arthroplasty-patients-100620201","NCT07354542","Effects of Different Relaxation Therapies on Pain and Sleep in Hip and Knee Arthroplasty Patients","Comparison of the Effects of Virtual Reality-based and Traditional Relaxation Therapy on Postoperative Pain and Sleep Quality in Patients Undergoing Hip and Knee Replacement Surgery","Inclusion Criteria:\n\n* Those who volunteered to participate in the research,\n* 18 years and older,\n* No diagnosed mental or sleep problems, epilepsy, or depression,\n* No vision, hearing, or speech problems,\n* Those who speak Turkish,\n* Knee and hip replacement surgery ,\n* No active nausea or vomiting prior to the virtual reality application,\n* According to the Numerical Rating Scale, the patient reports pain.\n* Those receiving analgesia treatment according to clinical protocol,\n* Anyone who owns a mobile phone or tablet capable of playing videos, using any brand of internet provider,\n* Patients who had not previously practiced breathing exercises were included .\n\nExclusion Criteria:\n\n* Having a problem that prevents communication,\n* Being admitted to the ward where the surgery and study were performed at another center,\n\n  . Complications develop after knee and hip replacement surgery,\n* Nausea and vomiting may occur during the procedure.\n* Wanting to withdraw from the research,\n* Experiencing chronic pain.",{"count":127,"type":22},82,[25],"Hip and knee replacement surgery is commonly performed in older adults. After surgery, many patients experience pain, limited movement, and sleep problems. These difficulties can make daily activities such as walking or climbing stairs more challenging and may reduce quality of life during recovery.\n\nRelaxation exercises are often used to help reduce pain and improve sleep after surgery. Virtual reality (VR) is a technology that provides a multisensory experience and may help people relax by shifting their attention away from pain and discomfort.\n\nThis study is designed to compare two different relaxation approaches used after hip and knee replacement surgery. One group of patients will perform relaxation exercises using virtual reality, while another group will perform traditional relaxation exercises. The study will examine pain levels and sleep quality in both groups.\n\nThe results of this study may help to better understand whether virtual reality-based relaxation can be used as an alternative or supportive method for managing pain and sleep problems after joint replacement surgery.",[131,132],"Osteoarthritis (OA) of the Hip","Osteoarthritis (OA) of the Knee",[134,135,136],"Postoperative Pain","Sleep Quality","Virtual Reality","2026-01-22",{"date":139,"type":40},"2026-01-23",{"date":141,"type":40},"2024-11-01",{"date":143,"type":22},"2026-01-30",{"name":46,"class":47},{"id":146,"slug":147,"hasResults":11,"nctId":148,"briefTitle":149,"officialTitle":150,"acronym":4,"eligibilityCriteria":151,"healthyVolunteers":56,"sex":17,"minAge":152,"maxAge":153,"enrollmentInfo":154,"targetDuration":4,"studyType":23,"phases":156,"briefSummary":157,"conditions":158,"keywords":160,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":166,"lastUpdatePostDateStruct":167,"startDateStruct":169,"completionDateStruct":171,"leadSponsor":173,"locationsCount":78},"100610631","exercise-and-physical-fitness-in-children-with-specific-learning-disabilities-100610631","NCT07230093","Exercise and Physical Fitness in Children With Specific Learning Disabilities","The Effect of Combined Exercise Training on Physical Fitness Parameters in Children With Specific Learning Disabilities","Inclusion Criteria:\n\n* Exercise Group: Children aged 7-14 years diagnosed with Specific Learning Difficulty (SLD), with signed parental consent and child assent form\n* Control Group: Children aged 7-14 years without SLD (healthy), with signed parental consent and child assent form\n\nExclusion Criteria:\n\n* Children with physical disabilities preventing participation\n* Children unable to cooperate with the assessments","7 Years","14 Years",{"count":155,"type":22},18,[25],"Specific learning disabilities (SLD) are characterized by difficulties in reading, comprehension, arithmetic, and written expression, often accompanied by impairments in motor skills, balance, and coordination. However, physical difficulties in children with SLD are often overlooked in educational settings, and parental awareness of these issues remains limited.\n\nThis study aims to examine the effect of an 8-week combined exercise program-including balance, strength, and stretching exercises-on the physical fitness of children aged 7-14 years with SLD. Participants will be randomly assigned to either an exercise group or a control group.\n\nThe exercise intervention will be conducted three times per week for 45 minutes per session over eight weeks. Physical fitness will be evaluated through standardized field-based measures of balance, strength, flexibility, and endurance before and after the intervention. Data will be analyzed using SPSS 26.0, employing Wilcoxon, Mann-Whitney U, independent t-test, and paired t-test as appropriate.\n\nThe study is expected to emphasize the importance of physical activity for children with SLD and promote the inclusion of physiotherapy-based exercise programs in individualized support plans.\n\nPrimary Outcome Question: Does an 8-week combined exercise program improve balance, strength, flexibility, and endurance-key components of physical fitness-in children with specific learning disabilities compared to a control group?",[159],"Learning Disabilities",[161,162,163,164,165],"Learning Disability","Physical Fitness","Combined Exercise","Children","Exercise Intervention","2025-11-13",{"date":168,"type":40},"2025-11-17",{"date":170,"type":22},"2025-11-25",{"date":172,"type":22},"2026-02-15",{"name":46,"class":47},{"id":175,"slug":176,"hasResults":11,"nctId":177,"briefTitle":178,"officialTitle":179,"acronym":4,"eligibilityCriteria":180,"healthyVolunteers":11,"sex":181,"minAge":182,"maxAge":4,"enrollmentInfo":183,"targetDuration":4,"studyType":23,"phases":185,"briefSummary":186,"conditions":187,"keywords":192,"overallStatus":110,"whyStopped":4,"lastUpdateSubmitDate":196,"lastUpdatePostDateStruct":197,"startDateStruct":199,"completionDateStruct":201,"leadSponsor":203,"locationsCount":78},"100600764","effects-of-hypopressive-exercises-on-urinary-incontinence-and-erectile-dysfunction-after-radical-prostatectomy-100600764","NCT07101731","Effects of Hypopressive Exercises on Urinary Incontinence and Erectile Dysfunction After Radical Prostatectomy","The Effects of Hypopressive Exercises on Urinary Incontinence and Erectile Dysfunction After Radical Prostatectomy: A Randomized Controlled Trial","Inclusion Criteria\n\n* Male individuals diagnosed with prostate cancer who have undergone radical prostatectomy\n* Experiencing both urinary incontinence and erectile dysfunction\n* Age \\> 55 years\n* A score of 24 or higher on the Mini-Mental State Examination (MMSE)\n* Literate (able to read and write)\n* Willingness to participate in the study (signed informed consent)\n* Ability to voluntarily contract pelvic floor muscles\n* Ability to cooperate with the assessments and interventions used in the study\n\nExclusion Criteria\n\n* History of urinary incontinence before surgery\n* Congenital abnormalities of the urinary system\n* Presence of neurological disorders\n* History of transurethral resection of the prostate (TURP)\n* Diagnosis of chronic obstructive pulmonary disease (COPD) and\u002For chronic restrictive pulmonary disease\n* History of inguinal hernia\n* Previous or current history of radiation therapy\n* Surgical or postoperative complications that prevent early physiotherapy intervention (e.g., urinary tract infection, bladder neck stenosis)","MALE","55 Years",{"count":184,"type":22},30,[25],"This randomized controlled trial investigates the effects of hypopressive exercises on urinary incontinence and erectile dysfunction in men following radical prostatectomy. Participants will be randomly assigned to one of two groups: a control group receiving home-based pelvic floor muscle exercises and an experimental group receiving both pelvic floor muscle exercises and supervised hypopressive exercises twice per week. The study aims to determine whether the addition of hypopressive techniques, which target coordinated activation of the pelvic floor and abdominal muscles without increasing intra-abdominal pressure, offers greater improvements in urinary and sexual function. Primary outcomes include pelvic floor muscle strength and endurance, while secondary outcomes include urinary incontinence severity, erectile function, and quality of life.",[188,189,190,191],"Prostate Cancer (Post Prostatectomy)","Urinary Incontinence","Erectile Dysfunction Following Radical Prostatectomy","Pelvic Floor Muscle Training",[193,189,194,191,195],"Radical Prostatectomy","Erectile Dysfunction","Hypopressive Exercises","2025-07-28",{"date":198,"type":40},"2025-08-03",{"date":200,"type":40},"2024-06-01",{"date":202,"type":22},"2025-11-15",{"name":46,"class":47},{"id":205,"slug":206,"hasResults":11,"nctId":207,"briefTitle":208,"officialTitle":208,"acronym":4,"eligibilityCriteria":209,"healthyVolunteers":11,"sex":17,"minAge":210,"maxAge":211,"enrollmentInfo":212,"targetDuration":4,"studyType":23,"phases":214,"briefSummary":215,"conditions":216,"keywords":4,"overallStatus":110,"whyStopped":4,"lastUpdateSubmitDate":218,"lastUpdatePostDateStruct":219,"startDateStruct":221,"completionDateStruct":223,"leadSponsor":225,"locationsCount":78},"100586197","the-effect-of-educational-animation-on-anxiety-and-fear-in-children-with-tympanostomy-tube-placement-in-pediatric-surgery-a-randomized-controlled-trial-100586197","NCT06912243","The Effect of Educational Animation on Anxiety and Fear in Children With Tympanostomy Tube Placement in Pediatric Surgery: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Being between 6-10 years old\n* Having ear tube surgery\n* Signing the informed consent form by the patient's legal guardian\n\nExclusion Criteria:\n\n* Previous surgical operation of the child\n* The child has had a cleft palate or lip operation before\n* Conditions that may prevent communication with parents (e.g. language problem)","6 Years","10 Years",{"count":213,"type":22},60,[25],"The study was planned as a randomized controlled experimental research to determine the effect of educational video screening on anxiety and fear in children. All children between the ages of 6-10 years old who underwent ear tube surgery will be included. Children will be randomly assigned to two groups (training video group, control group-standard care). In the training video group, a nurse will explain the process of ear tube surgery to the children with an educational video. The scenario of this educational animation will include information about the preoperative fears of a child who will undergo ear tube surgery, the structure of the ear, what they are most curious about, what the ear tube is, what will happen during and after surgery. In the control-standard care group, the standard information given to all children who had ear tube surgery in the relevant service will be given to the children in the control group. Data will be collected with the Sociodemographic Questionnaire, Child Anxiety Scale-Condition Child Fear Scale before and after surgery.",[217],"Pediatric Surgical Patients","2025-04-06",{"date":220,"type":40},"2025-04-08",{"date":222,"type":40},"2024-11-15",{"date":224,"type":22},"2025-12-15",{"name":46,"class":47},{"id":227,"slug":228,"hasResults":11,"nctId":229,"briefTitle":230,"officialTitle":231,"acronym":4,"eligibilityCriteria":232,"healthyVolunteers":11,"sex":17,"minAge":233,"maxAge":4,"enrollmentInfo":234,"targetDuration":4,"studyType":23,"phases":236,"briefSummary":237,"conditions":238,"keywords":240,"overallStatus":110,"whyStopped":4,"lastUpdateSubmitDate":245,"lastUpdatePostDateStruct":246,"startDateStruct":248,"completionDateStruct":250,"leadSponsor":252,"locationsCount":78},"100571528","the-effect-of-dual-task-training-on-balance-exercise-capacity-cognitive-status-and-quality-of-life-100571528","NCT06721429","The Effect of Dual-task Training on Balance, Exercise Capacity, Cognitive Status, and Quality of Life","The Effect of Dual-task Training on Balance, Exercise Capacity, Cognitive Status, and Quality of Life in Individuals With Type 2 Diabetes Mellitus","Inclusion Criteria:\n\n* Being followed up with a diagnosis of Type 2 Diabetes Mellitus for at least 6 months (fasting plasma glucose of 7.0 mmol\u002FL or higher)\n* Not having participated in any structured exercise program for at least 6 months prior.\n* Being willing to volunteer for the study\n\nExclusion Criteria:\n\n* Nephropathy\n* Retinopathy\n* Having dementia or Alzheimer's disease\n* Using a walking aid\n* Having ulceration\n* Using balance-curing drugs\n* Surviving myocardial infarction at least 6 months ago\n* Stable or unstable angina pectoris\n* Left ventricular ejection fraction below 40%\n* Peripheral arterial diseases\n* Resting blood pressure above 160\u002F100 mmHg\n* Body mass index above 35 kg\u002Fm2\n* Having a history of deep vein thrombosis, pulmonary embolism or stroke in the past","65 Years",{"count":235,"type":22},36,[25],"The aim of this study is to investigate the effects of dual-task training on balance, exercise capacity, cognitive function, and quality of life in individuals with Type 2 Diabetes Mellitus (DM). As a result of this study, it is hoped that dual-task training will be an alternative to single-task training in the rehabilitation of individuals with Type 2 DM, with the goal of preventing falls and supporting a more active lifestyle. Additionally, it is intended to include dual-task training in preventive physiotherapy approaches. The main questions the study aims to answer are as follows:\n\nIs dual-task training, conducted concurrently with exercise training, more effective in improving balance when compared to exercise training alone and the control group?\n\nIs dual-task training, conducted concurrently with exercise training, more effective in improving exercise capacity, cognitive function, and quality of life when compared to exercise training alone and the control group?\n\nThe researchers will compare the effects of dual-task training in individuals with Type 2 diabetes by comparing the participants in the single-task exercise training group and the control group. Participants will be randomized into the dual-task exercise training group, the single-task exercise training group, and the control group. Individuals in the training group will undergo exercise training three days a week for 8 weeks.",[239],"Diabetes Mellitus, Type 2",[241,242,243,244],"exercise","balance","exercise tolerance","Mental Status","2024-12-05",{"date":247,"type":40},"2024-12-06",{"date":249,"type":22},"2024-12-25",{"date":251,"type":22},"2025-05-28",{"name":46,"class":47},{"id":254,"slug":255,"hasResults":11,"nctId":256,"briefTitle":257,"officialTitle":258,"acronym":4,"eligibilityCriteria":259,"healthyVolunteers":56,"sex":17,"minAge":260,"maxAge":261,"enrollmentInfo":262,"targetDuration":4,"studyType":23,"phases":263,"briefSummary":264,"conditions":265,"keywords":4,"overallStatus":110,"whyStopped":4,"lastUpdateSubmitDate":268,"lastUpdatePostDateStruct":269,"startDateStruct":271,"completionDateStruct":273,"leadSponsor":275,"locationsCount":78},"100559665","effect-of-leg-and-heel-massage-on-pain-during-heel-blood-collection-newborns-100559665","NCT06567093","Effect of Leg and Heel Massage on Pain During Heel Blood Collection Newborns","Effect of Leg and Heel Massage on Pain Experienced During Heel Blood Collection and Physiological Parameters in Newborns: Randomized Controlled Study","Inclusion Criteria:\n\n* Gestational age is 38-41 weeks,\n* The birth weight of the newborn is \\>2500 g\n* Vital signs should be stable before the procedure,\n* Postanatal age is between 2-28 days,\n* There are no contraindications for the application of massage\n* Delivery of the newborn to the mother after birth\n* Permission of the parents of the newborn participating in the research\n* Fasting period less than 3 hours\u002Ffed 30 minutes before\n* A newborn who does not cry before heel blood is taken\n\nExclusion Criteria:\n\n* Newborns who need respiratory support,\n* Newborns with any neurological disorders (seizures)\n* Newborns using opioids or babies born to mothers using opioids\n* Newborns taking muscle relaxants, sedatives, analgesics\n* Babies with major congenital anomalies\n* Babies with an APGAR score of less than 7 in 5 minutes,\n* Newborns who have undergone any surgery\n* Newborns with birth trauma (especially rapid births)\n* There are situations that may prevent communication with parents (e.g. language problems).\n* problem)\n* Newborns planned to be transferred to another hospital","1 Day","28 Days",{"count":213,"type":22},[25],"This study was planned to evaluate the effect of leg and heel massage on newborns, the pain experienced during heel blood collection, and the effects on physiological parameters.\n\nH1: Newborn Infants Pain Scale scores are lower in leg and heel massage group than control group.\n\nH2: Heart rates are lower in leg and heel massage group than control group. H3: Oxygen saturation levels are higher in leg and heel massage group than control group.",[266,267],"Pain","Infant ALL","2024-08-20",{"date":270,"type":40},"2024-08-22",{"date":272,"type":40},"2024-08-15",{"date":274,"type":22},"2025-06-15",{"name":46,"class":47},{"id":277,"slug":278,"hasResults":11,"nctId":279,"briefTitle":280,"officialTitle":281,"acronym":4,"eligibilityCriteria":282,"healthyVolunteers":11,"sex":17,"minAge":86,"maxAge":283,"enrollmentInfo":284,"targetDuration":4,"studyType":23,"phases":286,"briefSummary":287,"conditions":288,"keywords":292,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":295,"lastUpdatePostDateStruct":296,"startDateStruct":298,"completionDateStruct":300,"leadSponsor":302,"locationsCount":4},"100513912","the-effect-of-progressive-relaxation-exercises-on-postoperative-pain-100513912","NCT05971641","The Effect of Progressive Relaxation Exercises on Postoperative Pain","The Effect of Progressive Relaxation Exercises on Postoperative Pain Intensity, Sleep Quality, and Recovery in Patients Undergoing Total Knee Arthroplasty","Inclusion Criteria:\n\n* 18 years and older,\n* Without diagnosed mental disorders,\n* Without visual, hearing, and speech impairments,\n* Proficient in Turkish,\n* Diagnosed with gonarthrosis and scheduled for total knee replacement,\n* No postoperative complications following total knee replacement surgery,\n* Literate with an educational level,\n* Pain level of 4 or above on the NRS,\n* Receiving analgesic treatment according to the clinical protocol,\n* Ownership of a mobile device such as a smart phone or tablet capable of accessing internet-based video content with the latest technology from any brand,\n* Patients without diagnosed sleep problems will be included in the thesis study.\n\nExclusion Criteria:\n\n* Illiterate individuals,\n* Under the age of 18,\n* Having a condition that hinders communication,\n* Referred from another center after surgery,\n* Pain level of 4 or below on the NRS,\n* Developing complications after total knee replacement surgery,\n* Receiving analgesic treatment and methods outside of the clinical protocol,\n* Not owning a mobile device such as a smart phone or tablet capable of accessing internet-based video content with the latest technology from any brand,\n* Having diagnosed sleep problems,\n* Having diagnosed mental disorders, will be excluded from the scope of the thesis study.","90 Years",{"count":285,"type":22},96,[25],"The indicators of patient recovery in the postoperative period include sleep, physical functionality, mental health, cognitive functionality, pain, and psychosocial functionality.\n\nThis thesis aims to investigate the effects of progressive relaxation exercises on postoperative pain intensity, sleep quality, and recovery in patients undergoing total knee arthroplasty.This study, designed as a randomized controlled experimental study, will be conducted between September 1, 2023, and August 1, 2024, at ÇAYCUMA State Hospital in ZONGULDAK province, Turkey, among patients undergoing total knee arthroplasty. A total of 96 patients will be recruited based on the sample size calculated using G-power analysis. Through block randomization, 48 patients will be assigned to the intervention group and 48 patients to the control group. Data will be collected using the Numeric Rating Scale for pain, the Richard-Campbell Sleep Scale, a sleep tracker smart wristband to measure sleep quality and duration, the Postoperative Recovery Index, and a Patient Information Form.",[289,290,291],"Arthroplasty","Replacement","Knee",[293,294],"Total Knee Replacement","Progressive relaxation exercises","2024-07-28",{"date":297,"type":40},"2024-07-30",{"date":299,"type":22},"2024-12-09",{"date":301,"type":22},"2025-09-01",{"name":46,"class":47},""]