[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"geriatric-assessment\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:geriatric-assessment":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,19,0,[8,45,77,106,133,158,184,212,237,265,291,318,363,385,405,427,448,481,508],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":29,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100592012","practical-geriatric-assessment-in-older-adults-with-non-small-cell-lung-cancer-undergoing-stereotactic-body-radiation-therapy-100592012",false,"NCT06987890","Practical Geriatric Assessment in Older Adults With Non-Small Cell Lung Cancer Undergoing Stereotactic Body Radiation Therapy","Lung-GAP","Inclusion Criteria:\n\n* Age ≥ 65 years old at time of study enrollment.\n* Radiographically or pathologically confirmed stage I-II non-small cell lung cancer.\n* All patients must have undergone appropriate complete imaging of their cancer consistent with the standard of care.\n* Patient is expected to undergo stereotactic body radiation therapy (SBRT)\n* Able to read questions in English or willing to complete survey questionnaires with the assistance of an interpreter.\n\nExclusion Criteria:\n\n* There are no exclusion criteria.","ALL","65 Years",{"count":19,"type":20},64,"ESTIMATED","INTERVENTIONAL",[23],"NA","National guidelines recommend that older adults with cancer undergo a special health assessment before starting cancer treatment. This type of assessment evaluates physical function, nutrition, social support, psychological well-being, medical conditions (both cancer-related and non-cancer-related), and cognitive function. The results can help doctors make better treatment decisions and determine whether additional support services-such as nutrition counseling, physical therapy, or social work-would be beneficial. Even though these assessments are recommended, they are not typically used because they need to be performed by a specialist and can take over an hour to complete. Given these challenges, a 10-15-minute assessment called the Practical Geriatric Assessment (PGA) was recently developed. The PGA can be completed by any healthcare provider and helps identify older adults who may need extra support alongside their cancer treatment. While the PGA has the potential to make geriatric assessments more accessible, the investigators do not yet know whether patients will find it useful or easy to complete.\n\nAdditionally, it is unclear whether using the PGA will lead to more referrals for recommended supportive care services. This study aims to address these questions. The investigators will evaluate whether using the PGA impacts the number of patients referred to recommended supportive care services. Investigators will also evaluate how participants feel about completing the PGA, including how easy or difficult it is, and to assess the feasibility of implementing this survey on a larger scale. Finally, the investigators will use facial photographs and audio-visual data from the PGA to develop and evaluate artificial intelligence algorithm(s) to identify vulnerable patients who might benefit from additional supportive care services; namely, FaceAge, a validated deep learning model capable of estimating biological age from still facial images.",[26,27,28],"Lung Cancer (NSCLC)","Geriatric Assessment","Stereotactic Body Radiation Therapy (SBRT)",[30,31],"Lung Cancer","Geriatric","RECRUITING","2026-06-24",{"date":35,"type":36},"2026-06-25","ACTUAL",{"date":38,"type":36},"2025-05-26",{"date":40,"type":20},"2026-06-26",{"name":42,"class":43},"Brigham and Women's Hospital","OTHER",1,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":51,"eligibilityCriteria":52,"healthyVolunteers":11,"sex":16,"minAge":53,"maxAge":4,"enrollmentInfo":54,"targetDuration":4,"studyType":56,"phases":4,"briefSummary":57,"conditions":58,"keywords":61,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":69,"completionDateStruct":71,"leadSponsor":73,"locationsCount":76},"100613958","aspects-of-adjuvant-cdk46-inhibitors-in-older-breast-cancer-patients---focusing-on-geriatric-screening-100613958","NCT07273357","Aspects of Adjuvant CDK4\u002F6 Inhibitors in Older Breast Cancer Patients - Focusing on Geriatric Screening","Follow-Up After adjuvanT CDK4\u002F6i Use in oldeR brEast Cancer Patients - Aspects on Geriatric Screening, Toxicities, and Quality of Life (FUTURE)","FUTURE","Inclusion Criteria:\n\n* ≥70 years old\n* Female\u002Fmale\n* Completed surgery (primary or after neoadjuvant therapy)\n* Starting adjuvant CDK4\u002F6i and endocrine therapy\n* Cognitive performance to be able answer questionaries\n* No language difficulties\n\nExclusion Criteria:\n\n* Impaired cognitive function not able to understand the study intention or perform questionaries\n* Declining adjuvant CDK4\u002F6i","70 Years",{"count":55,"type":20},200,"OBSERVATIONAL","Older breast cancer patients should not be categorically excluded from adjuvant therapies, including the recommended CDK4\u002F6 inhibitors (CDK4\u002F6i) administered in combination with endocrine therapy. Nevertheless, this population frequently presents with comorbidities that may increase susceptibility to treatment-related toxicities, including impacts on quality of life, which must be carefully considered when selecting therapeutic regimens. Given the limited representation of older patients in the clinical trials behind the recommendations for adjuvant CDK4\u002F6i therapy, coupled with the uncertain magnitude of clinical benefit and the reported rates of toxicity and treatment discontinuation, it is essential to critically evaluate both efficacy and safety in this specific patient subgroup. National and international guidelines recommend the integration of geriatric assessments into routine clinical practice to facilitate individualized treatment decisions; however, such assessments are not yet widely implemented in many oncology departments and are not routinely in use to guide adjuvant CDK4\u002F6i therapy.\n\nThis study aims to investigate the implementation of geriatric assessments in older breast cancer patients (≥70 years) and to examine multiple dimensions of CDK4\u002F6i treatment in this cohort, including short- and medium-term effects on quality of life, dose intensity, and clinical outcomes. By doing so, the investigators seek to more accurately delineate the benefits and risks of adjuvant CDK4\u002F6i therapy in this specific patient population.",[27,59,60],"Adjuvant Drug Therapy","Breast Cancer Early Stage Breast Cancer (Stage 1-3)",[62,63,64,65],"Older patients","Geriatric screening","Adjuvant CDK4\u002F6 inhibitors","Breast cancer","2026-06-09",{"date":68,"type":36},"2026-06-10",{"date":70,"type":36},"2026-04-01",{"date":72,"type":20},"2039-08-01",{"name":74,"class":75},"Region Jönköping County","OTHER_GOV",5,{"id":78,"slug":79,"hasResults":11,"nctId":80,"briefTitle":81,"officialTitle":82,"acronym":4,"eligibilityCriteria":83,"healthyVolunteers":11,"sex":16,"minAge":84,"maxAge":4,"enrollmentInfo":85,"targetDuration":4,"studyType":21,"phases":87,"briefSummary":88,"conditions":89,"keywords":93,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":97,"lastUpdatePostDateStruct":98,"startDateStruct":100,"completionDateStruct":102,"leadSponsor":104,"locationsCount":44},"100552157","the-impact-of-geriatric-assessment-on-the-treatment-plan-of-elderly-patients-with-t2dm-100552157","NCT06469437","The Impact of Geriatric Assessment on the Treatment Plan of Elderly Patients With T2DM","The Impact of Geriatric Assessment on the Treatment Plan of Elderly Patients With Type 2 Diabetes Mellitus: a Randomized Clinical Trial.","Inclusion Criteria:\n\n* Age 60 years or older\n* Diagnostic of type 2 diabetes mellitus according to American Diabetes Association criteria\n* Patients under follow-up in a specialized endocrinology outpatient clinic\n* Patients who have a glycated hemoglobin measurement of up to three months\n\nExclusion Criteria:\n\n* Lack of consent for research participation from the patient or the physician\n* Patients classified as Clinical Frailty Scale 9.","60 Years",{"count":86,"type":20},220,[23],"Introduction: With the aging of the world population and the increasing incidence of type 2 diabetes mellitus (T2DM) with age, the number of elderly individuals living with diabetes has been considerably rising. It is known that uncontrolled T2DM negatively impacts various health outcomes, including geriatric outcomes such as sarcopenia, frailty, immobility, incontinence, and infections. Current medical literature fails to establish appropriate glycemic targets for different elderly profiles. Although guidelines emphasize the need to individualize targets, there is no concise tool to identify which individuals benefit from each therapeutic approach. Data suggest that frailty is the best predictor of negative outcomes in elderly patients living with T2DM. The Clinical Frailty Scale (CFS) and the 10-minute Targeted Geriatric Assessment (TaGA-10) are validated tools for prognosis in elderly patients and for identifying frail elderly individuals.\n\nMethods: Randomized controlled trial. Elderly individuals diagnosed with T2DM at a tertiary care outpatient clinic will be included. All enrolled patients will undergo geriatric assessment using CFS, TaGA-10, and Charlson Comorbidity Index. Patients will be randomized into usual care and intervention groups, and the intervention involves providing the geriatric assessment to the care team to support their decisions. The adequacy of the therapeutic approach will be measured in one week by reviewing the consult record or interviewing the physician. The clinical impact on the frequency of hypoglycemia, falls, infections, hospitalizations, and mortality will be evaluated at 3 and 6 months by telephone interviews.\n\nDiscussion: Current guidelines recommend using age, comorbidities, cognitive, and functional status to individualize therapeutic targets in elderly patients with T2DM; however, it is possible that these variables alone may not be sufficient to classify all elderly individuals in their complexity adequately. A tool with such power and easy to use in clinical practice is necessary.",[90,91,92,27],"Type2diabetes","Frail Elderly Syndrome","Frailty",[94,92,95,96],"Type 2 diabetes","Geriatric assessement","Glycated hemoglobin","2026-05-27",{"date":99,"type":36},"2026-05-29",{"date":101,"type":36},"2024-07-05",{"date":103,"type":20},"2028-12-31",{"name":105,"class":43},"Hospital de Clinicas de Porto Alegre",{"id":107,"slug":108,"hasResults":11,"nctId":109,"briefTitle":110,"officialTitle":111,"acronym":112,"eligibilityCriteria":113,"healthyVolunteers":114,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":115,"targetDuration":4,"studyType":56,"phases":4,"briefSummary":117,"conditions":118,"keywords":4,"overallStatus":123,"whyStopped":4,"lastUpdateSubmitDate":124,"lastUpdatePostDateStruct":125,"startDateStruct":127,"completionDateStruct":129,"leadSponsor":131,"locationsCount":44},"100636818","implementation-of-a-clinical-decision-support-system-in-primary-care-for-the-screening-and-assessment-of-frailty-in-patients-aged-65-and-over-100636818","NCT07570628","Implementation of a Clinical Decision Support System in Primary Care for the Screening and Assessment of Frailty in Patients Aged 65 and Over","Implementation of a Clinical Decision Support System in Primary Care for the Screening and Assessment of Frailty in Patients Aged 65 and Over: A Real-World Prospective Cohort Study","FRAGICLIC","Inclusion Criteria:\n\n* Patients aged 65 years or older\n* Patient or trusted person who provided oral non-opposition after receiving full information about the protocol\n* Managed by the general practitioner if the patient or nurse during the study period. If patients are assessed by a nurse : Patients whose general practitioner is a participating physician in the study\n\nExclusion Criteria:\n\n* Patients unable to express non-opposition or without a trusted person available to express non-opposition\n* Patients whose general practitioner (GP) is not a participating GP in the study\n* Patients or trusted persons who do not speak French",true,{"count":116,"type":20},726,"This observational study aims to evaluate the real-life use of a digital tool (Fragiclic) by general practitioners (GPs) and nurses to screen and assess frailty in adults aged 65 and over. Frailty is a syndrome that increases the risk of loss of autonomy, falls, hospitalizations, or death. The tool includes simple screening questionnaires (such as SEGAm) and a comprehensive assessment (CGA - Comprehensive Geriatric Assessment) to better manage patients' health.\n\nThe main question it aims to answer is:\n\n* What proportion of patients aged 65 and over will benefit from frailty screening or assessment using Fragiclic over 12 months?\n\nA secondary question is\n\n\\- Does the use of Fragiclic reduce the risk of unplanned hospitalizations or death in these patients?\n\nFor the secondary question, researchers will compare patients who received screening or assessment (with or without a Personalized Care Plan (PCP)) to those who did not, to determine if Fragiclic improves their health outcomes.\n\nParticipants will not have additional tasks: Their GP or nurse will use Fragiclic during routine consultations. Some patients may be asked to provide information about their health or quality of life (via their healthcare provider).\n\nAll data will be collected anonymously and securely",[119,120,27,121,122],"Frailty at Older Adults","Primary Care","Implementation Research","Interprofessional Collaboration","NOT_YET_RECRUITING","2026-05-11",{"date":126,"type":36},"2026-05-13",{"date":128,"type":20},"2027-01-02",{"date":130,"type":20},"2029-01-02",{"name":132,"class":43},"CNGE Conseil",{"id":134,"slug":135,"hasResults":11,"nctId":136,"briefTitle":137,"officialTitle":138,"acronym":4,"eligibilityCriteria":139,"healthyVolunteers":114,"sex":16,"minAge":140,"maxAge":4,"enrollmentInfo":141,"targetDuration":4,"studyType":21,"phases":143,"briefSummary":144,"conditions":145,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":149,"lastUpdatePostDateStruct":150,"startDateStruct":152,"completionDateStruct":154,"leadSponsor":156,"locationsCount":44},"100530280","implementation-pilot-of-preoperative-cga-before-major-surgery-100530280","NCT06184724","Implementation Pilot of Preoperative CGA Before Major Surgery","Implementation Pilot of Preoperative CGA Referral Process for Older Patients Undergoing Major Surgery","Inclusion Criteria:\n\n1. Patient aged 80 or older who is scheduled for an elective inpatient major surgery\n2. Providers working in a clinic (aged 18 and older) where pCGA is performed or a related anesthesia pre-operative clinic\n3. Surgeons (adults older than 18) with a patient aged 80 or older who is scheduled for an elective inpatient major surgery\n\nExclusion criteria:\n\n* None","18 Years",{"count":142,"type":20},42,[23],"The goal of this clinical trial is to test whether a new implementation package can help older adults prepare for major surgery. The main question it aims to answer is: Can the implementation package help give more people access to this resource? Participants will be in two groups: older adults who are planning a major surgery and their medical and surgical healthcare providers. The results will be compared to a historic baseline.",[146,27,147,148],"Surgery","Health Services Research","Implementation Science","2026-03-18",{"date":151,"type":36},"2026-03-19",{"date":153,"type":36},"2026-01-28",{"date":155,"type":20},"2029-04",{"name":157,"class":43},"University of Wisconsin, Madison",{"id":159,"slug":160,"hasResults":11,"nctId":161,"briefTitle":162,"officialTitle":163,"acronym":164,"eligibilityCriteria":165,"healthyVolunteers":11,"sex":16,"minAge":166,"maxAge":4,"enrollmentInfo":167,"targetDuration":4,"studyType":21,"phases":169,"briefSummary":170,"conditions":171,"keywords":172,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":175,"lastUpdatePostDateStruct":176,"startDateStruct":177,"completionDateStruct":179,"leadSponsor":181,"locationsCount":183},"100611152","evaluation-of-grampa-score-measuring-motor-abilities-of-elderly-patients-100611152","NCT07236866","Evaluation of GRAMPA Score Measuring Motor Abilities of Elderly Patients","Prospective, Single-center Interventional Study to Assess the Reliability of the GRAMPA Score, Measuring the Graduation of Motor Abilities of the Elderly Patients Hospitalised","GRAMPA","Inclusion Criteria:\n\n1. Age ≥ 75 years\n2. Patients hospitalized in the geriatrics department of the Grenoble Mutualist Hospital Group\n3. Comprehension of the French language (understanding of instructions)\n4. Signature of free and informed consent\n\nExclusion Criteria:\n\n1. Patients whose sensory and\u002For mental capacities do not allow them to understand the instructions for carrying out transfers.\n2. Patients with medical or surgical contraindications making it impossible to carry out transfers.\n3. Patients under legal protection or unable to express their consent.","75 Years",{"count":168,"type":20},55,[23],"In the field of geriatrics, the Standardized Geriatric Approach (SGA) which is the benchmark for assessing elderly patients, consists of evaluating the medical, psychological and functional capacity dimensions of the elderly subject, among others.\n\nAfter a review of the literature, investigators were unable to find any scales that could study the ability to perform basic movements in a comprehensive and graded manner.\n\nScores that do assess certain aspects of motor abilities are not comprehensive, and are often based on self-reporting by the elderly or their relatives :\n\n* The AGGIR grid assesses dependency on the basis of activities performed or not performed. In addition, all basic movements are grouped together in a single item, which does not provide detailed information on the capabilities of elderly people.\n* The ADL score assesses activities of daily living, based on what patients declare. Only one item concerns basic movements, without detailing them.\n* The Tinetti score and Time up and go do not assess all basic movements, and require the patient to be able to stand to provide relevant information, whereas many geriatrics patients are unable to stand.\n\nThus, investigators created a score to assess motor abilities more comprehensively that will include the following basic movements:\n\n* Getting up in bed\n* Turning on one side in bed\n* Sitting at the edge of the bed\n* Stand up\n* Move around a small perimeter (bedroom)\n* Sitting up\n* Return to bed\n\nThe main objective is to evaluate of this study is to determine the inter-rater reliability of the GRAMPA score in elderly patients hospitalized in a geriatrics department.",[27],[173,174],"motor skills","rehabilitation","2026-03-16",{"date":149,"type":36},{"date":178,"type":36},"2025-11-07",{"date":180,"type":20},"2027-11-01",{"name":182,"class":43},"Groupe Hospitalier Mutualiste de Grenoble",2,{"id":185,"slug":186,"hasResults":11,"nctId":187,"briefTitle":188,"officialTitle":189,"acronym":190,"eligibilityCriteria":191,"healthyVolunteers":11,"sex":16,"minAge":140,"maxAge":192,"enrollmentInfo":193,"targetDuration":4,"studyType":56,"phases":4,"briefSummary":195,"conditions":196,"keywords":202,"overallStatus":123,"whyStopped":4,"lastUpdateSubmitDate":204,"lastUpdatePostDateStruct":205,"startDateStruct":206,"completionDateStruct":208,"leadSponsor":210,"locationsCount":44},"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","100 Years",{"count":194,"type":20},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.",[197,198,199,31,27,200,201],"Operative Surgical Procedures","Aged","Aged 65 Years or Older","Postoperative Care","Postoperative Complications",[197,198,203,27,200,201],"Geriatrics","2026-01-20",{"date":153,"type":36},{"date":207,"type":20},"2026-08-01",{"date":209,"type":20},"2027-12-31",{"name":211,"class":43},"Hospital Departamental de Villavicencio",{"id":213,"slug":214,"hasResults":11,"nctId":215,"briefTitle":216,"officialTitle":216,"acronym":217,"eligibilityCriteria":218,"healthyVolunteers":114,"sex":16,"minAge":219,"maxAge":220,"enrollmentInfo":221,"targetDuration":222,"studyType":56,"phases":4,"briefSummary":223,"conditions":224,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":228,"lastUpdatePostDateStruct":229,"startDateStruct":231,"completionDateStruct":233,"leadSponsor":235,"locationsCount":44},"100580188","validity---reliability-of-berg-balance-scale-in-albanian-population-100580188","NCT06834048","Validity - Reliability of Berg Balance Scale in Albanian Population","BERGA","Inclusion Criteria:\n\n* Postural pain\n* muscular contractions\n\nExclusion Criteria:\n\n* mixed fractures\n* trauma\n* luxation\n* tumor","50 Years","80 Years",{"count":55,"type":20},"7 Days","Cross-cultural adaptation, validity and Reliability of Berg Balance Scale in Albanian population",[225,226,227,27],"Balance Assessment","Balance Control in Elderly","Balance Changes","2025-11-15",{"date":230,"type":36},"2025-11-19",{"date":232,"type":36},"2025-01-17",{"date":234,"type":20},"2026-01-30",{"name":236,"class":43},"Universidad Católica San Antonio de Murcia",{"id":238,"slug":239,"hasResults":11,"nctId":240,"briefTitle":241,"officialTitle":242,"acronym":243,"eligibilityCriteria":244,"healthyVolunteers":11,"sex":16,"minAge":53,"maxAge":4,"enrollmentInfo":245,"targetDuration":4,"studyType":56,"phases":4,"briefSummary":246,"conditions":247,"keywords":250,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":255,"lastUpdatePostDateStruct":256,"startDateStruct":258,"completionDateStruct":260,"leadSponsor":262,"locationsCount":264},"100582999","practical-geriatric-assessment-pga-implementation-strategies-and-correlative-evaluations-pace-70-100582999","NCT06870617","Practical Geriatric Assessment (PGA) Implementation Strategies and Correlative Evaluations (PACE-70)","Practical Geriatric Assessment (PGA) Implementation Strategies and Correlative Evaluations for Older Adults With Cancer (PACE-70): A Hybrid Implementation-effectiveness Study","PACE-70","For PGA Implementation Cohort, patients must meet the following criteria:\n\n1. Age greater than or equal to 70 years.\n2. Diagnosis of advanced or metastatic solid malignancy\n3. Initiating a new line of palliative-intent systemic therapy with a prevalence of grade 3 toxicity exceeding 50%.\n\nFor Correlative Analysis Cohort, patients must additionally meet the following criteria:\n\n1. Must read and speak English and be able to fill out surveys\n2. Ability to walk independently or with the use of an assistive device (e.g., walker, cane)\n3. Consents to participate in correlative analysis cohort with Fitbit monitoring, body composition analysis, and self-report surveys\n4. Have a smartphone able to operate with the Fitbit\n\nFor PGA Implementation Cohort, there are no specific exclusion criteria other than not meeting inclusion criteria.\n\nFor Correlative Analysis Cohort, patients will be excluded if meeting any of the following criteria:\n\n1. Unable to effectively read and speak English\n2. Reliance on a wheelchair, ECOG of 3 or above, clinically bedbound, or unable to walk without assistance every day for the past 7 days (ECOG 3 is confined to bed or chair for more than 50% of waking hours)\n3. Concurrent enrollment in a therapeutic clinical trial (as clinical trials often have a substantial symptom-reporting structure). Non-therapeutic clinical trial enrollment is permitted\n4. Lack of clinician consent to approach patient",{"count":194,"type":20},"The use of a geriatric assessment to inform oncologic care for older persons with cancer is an evidence-based practice that improves patient-clinician communication, reduces treatment-related toxicity, and is recommended by national guidelines. However, the implementation of a geriatric assessment can be time-consuming and burdensome, leading to suboptimal use in clinical practice. Developed and endorsed by the American Society for Clinical Oncology (ASCO), the Practical Geriatric Assessment (PGA) is designed to improve clinical usability and adoption, but its implementation in real-world settings has not been evaluated. The PACE-70 study aims to evaluate PGA implementation and resultant chemotherapy dose modification among older adults with advanced cancer treated in a community setting. An exploratory aim will evaluate how the PGA, body composition (via abdominal computed tomography scan) and step count monitoring (via FitBit) correlate with chemotherapy toxicity and other clinical outcomes.",[27,248,249],"Advanced Cancer","Toxicity",[243,251,252,253,254],"Practical geriatric assessment","body composition in cancer","step count in cancer","Start low go slow","2025-10-02",{"date":257,"type":36},"2025-10-03",{"date":259,"type":36},"2025-07-01",{"date":261,"type":20},"2026-10-01",{"name":263,"class":43},"Abramson Cancer Center at Penn Medicine",3,{"id":266,"slug":267,"hasResults":11,"nctId":268,"briefTitle":269,"officialTitle":269,"acronym":270,"eligibilityCriteria":271,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":272,"targetDuration":4,"studyType":56,"phases":4,"briefSummary":273,"conditions":274,"keywords":276,"overallStatus":123,"whyStopped":4,"lastUpdateSubmitDate":282,"lastUpdatePostDateStruct":283,"startDateStruct":285,"completionDateStruct":287,"leadSponsor":289,"locationsCount":44},"100585993","transcultural-and-psychometric-validation-of-the-lubben-social-network-scale-in-older-adults-living-in-the-french-west-indies-100585993","NCT06909591","Transcultural and Psychometric Validation of the Lubben Social Network Scale in Older Adults Living in the French West Indies","VALLUB","Inclusion Criteria:\n\n* Patient ≥ 65 years old,\n* Hospitalized (Geriatric Day Hospital (HDJ) or Geriatric Medical Care and Rehabilitation Service (SMT)), or seen in geriatric external consultation,\n* MMS ≥ 20,\n* Patient able to understand and answer a self-administered questionnaire in French,\n* Patient having been informed of the research,\n* Patient agreeing to participate in the study.\n\nExclusion Criteria:\n\n* Patient with sensory disorders preventing completion of the questionnaire,\n* Patient unable to consent to participate in the study,\n* Patient under legal protection, guardianship, or curatorship,\n* Patient who has refused to participate in the study.",{"count":194,"type":20},"Social isolation and loneliness are common among older adults. They are associated with high morbidity and mortality, with an impact comparable to that of other known risk factors such as obesity, a sedentary lifestyle, smoking, etc.\n\nTo date, there is no tool to measure social isolation and loneliness for patients living in the French West Indies. Applying unadapted and unvalidated tools to them without taking into account local ethnocultural realities would be risky.\n\nThe investigators believe it is necessary to adapt the scales used to measure social isolation and loneliness for a population living in the French West Indies.\n\nThrough this study, the investigators propose adapting the Lubben Social Network Scale, a social isolation questionnaire, for this population and conducting its psychometric validation.",[27,275],"Patients Over 65 Years Old",[203,277,278,279,280,281],"Lubben Social Network Scale","Transcultural validation","Psychometric validation","Martinique","French West Indies","2025-06-12",{"date":284,"type":36},"2025-06-15",{"date":286,"type":20},"2025-09-01",{"date":288,"type":20},"2027-12-01",{"name":290,"class":43},"University Hospital Center of Martinique",{"id":292,"slug":293,"hasResults":11,"nctId":294,"briefTitle":295,"officialTitle":296,"acronym":297,"eligibilityCriteria":298,"healthyVolunteers":11,"sex":16,"minAge":299,"maxAge":4,"enrollmentInfo":300,"targetDuration":4,"studyType":56,"phases":4,"briefSummary":302,"conditions":303,"keywords":306,"overallStatus":123,"whyStopped":4,"lastUpdateSubmitDate":309,"lastUpdatePostDateStruct":310,"startDateStruct":312,"completionDateStruct":314,"leadSponsor":316,"locationsCount":44},"100588841","geriatric-assessment-ga-for-elderly-patients-undergoing-allo-hsct-100588841","NCT06946654","Geriatric Assessment (GA) for Elderly Patients Undergoing Allo-HSCT","Geriatric Assessment (GA) for Elderly Patients Undergoing Allogeneic Hematopoietic Stem Cell Transplantation: a Prospective Study.","GA","Inclusion Criteria:\n\n* (a)Age ≥55 years.\n* (b)Hematologic disorders with established indications for transplantation, including malignant and non-malignant hematologic diseases. (c)Willingness to provide informed consent.\n\nExclusion Criteria: (a)Pregnancy. (b) Uncontrolled active infection. (c) Lack of informed consent. (d)Deemed ineligible for transplantation after investigator assessment","55 Years",{"count":301,"type":20},176,"This comprehensive, multidimensional evaluation assesses patient-related factors, disease-related factors, donor-related factors, and treatment-related factors. The study aims to identify potential risk factors influencing transplant outcomes in elderly patients and enhance the outcomes of allo-HSCT.",[304,27,305],"Elderly","ALLOGENEIC HEMATOPOIETIC STEM CELL TRANSPLANTATION",[307,27,308],"elderly","allo-HSCT","2025-05-09",{"date":311,"type":36},"2025-05-11",{"date":313,"type":20},"2025-05-20",{"date":315,"type":20},"2027-03-31",{"name":317,"class":43},"Peking University People's Hospital",{"id":319,"slug":320,"hasResults":11,"nctId":321,"briefTitle":322,"officialTitle":323,"acronym":4,"eligibilityCriteria":324,"healthyVolunteers":11,"sex":16,"minAge":84,"maxAge":220,"enrollmentInfo":325,"targetDuration":4,"studyType":21,"phases":327,"briefSummary":328,"conditions":329,"keywords":340,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":354,"lastUpdatePostDateStruct":355,"startDateStruct":357,"completionDateStruct":359,"leadSponsor":361,"locationsCount":44},"100520408","the-effect-of-motor-image-training-on-balance-performance-in-geriatric-individuals-100520408","NCT06056180","The Effect of Motor Image Training on Balance Performance in Geriatric Individuals","Investigation of the Effects of Motor Imagery Training Given With Action Observation on Balance Performance in Geriatric Individuals","Inclusion Criteria:\n\n1. To be between 60-80 years old\n2. Having the ability to speak, read, understand and write Turkish\n3. To have the cognitive skills to understand and apply the trainings to be applied in the study (with ≥ 24 points from the Mini Mental State Test)\n4. Being able to do activities of daily living independently\n5. Being able to walk independently (without using a walking aid and at least 10 meters)\n6. Having a body mass index of \\\u003C35 kg\u002Fm2 (not being severely obese or morbidly obese)\n\nExclusion Criteria:\n\n1. Having visual, hearing and sensory impairment\n2. To have had a trauma, lesion or surgery that may affect balance and musculoskeletal system in the last 6 months\n3. Having a history of 2 ≥ falls in the last 6 months\n4. Having any chronic lower extremity pain\n5. Having an acute or chronic illness that may cause problems with balance and falling\n6. Being diagnosed with sensory, vestibular and cerebellar ataxia\n7. Being on any medication that may cause problems with balance, focus, attention and falling.\n8. Exercising regularly, which may affect performance results\n9. To stop participating in the study for any reason",{"count":326,"type":20},46,[23],"The goal of this study \\[type of study: clinical trial\\] is to was planned to investigate the effect of motor imagery training given to geriatric individuals with action observation on their balance performance and to compare these two methods.\n\nThe main questions it aims to answer are:\n\n1. Is virtual reality-based balance training given together with action observation and motor imagery for six weeks in geriatric individuals more effective in improving static balance than virtual reality-based balance training given alone?\n2. Is virtual reality-based balance training given together with action observation and motor imagery for six weeks in geriatric individuals more effective in improving dynamic balance than virtual reality-based balance training given alone?\n3. Is virtual reality-based balance training given together with motor imagery for six weeks in geriatric individuals more effective in increasing balance confidence than virtual reality-based balance training given alone?\n\n46 geriatric individuals will be randomized into 2 groups. Along with action observation, motor imagery training and virtual reality-based balance training will be given to the study group. On the other hand, only virtual reality-based balance training will be given to the control group. All assessments will be repeated before and after the trainings. The trainings will be applied 2 days a week for 6 weeks. Each training session; 25 minutes for the control group and 45 minutes for the study group.",[330,331,332,333,334,27,335,336,337,338,339],"Imagery (Psychotherapy)","Postural Control","Postural Balance","Virtual Reality Therapy","Surface Electromyography","Physical Therapy Techniques","Physical Therapy","Healthy Ageing","Healthy Aging","Falling",[341,342,343,344,345,346,347,348,349,350,351,352,353],"visual motor imagery","kinesthetic motor imagery","postural control","virtual reality therapy","interactive video games","balance platform with pressure sensor","surface electromyography","balance confidence","fall risk","mobility","cognitive processing speed","smartphone gyroscope sensor dataset","action observation","2025-05-05",{"date":356,"type":36},"2025-05-08",{"date":358,"type":36},"2023-11-01",{"date":360,"type":20},"2025-12",{"name":362,"class":43},"Muğla Sıtkı Koçman University",{"id":364,"slug":365,"hasResults":11,"nctId":366,"briefTitle":367,"officialTitle":367,"acronym":368,"eligibilityCriteria":369,"healthyVolunteers":11,"sex":16,"minAge":166,"maxAge":4,"enrollmentInfo":370,"targetDuration":4,"studyType":21,"phases":372,"briefSummary":373,"conditions":374,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":377,"lastUpdatePostDateStruct":378,"startDateStruct":380,"completionDateStruct":382,"leadSponsor":383,"locationsCount":44},"100555518","geriatric-assessment-at-discharge-from-the-intensive-care-unit-in-patients-aged-75-years-and-older-a-feasibility-study-100555518","NCT06513130","Geriatric Assessment at Discharge From the Intensive Care Unit in Patients Aged 75 Years and Older: a Feasibility Study","PreGEDI","Inclusion Criteria:\n\n* Patients over 75 years of age\n* Admitted to the intensive care unit, for whatever reason, and having survived their stay, considered as leaving the intensive care unit.\n* Subjects affiliated to a health insurance scheme\n* Able to understand the aims and risks of the research and to give dated, signed informed consent,\n* In the event of confusion on leaving the intensive care unit, a close relative available to give dated, signed informed consent, with the patient's consent collected as soon as his or her condition permits.\n\nExclusion Criteria:\n\n* Protected subject as defined by law: safeguard of justice, guardianship or curatorship procedures\n* Subject moribund, or whose life expectancy as estimated by the clinician in charge is less than 1 month\n* Patient not living in Bas-Rhin (visit to M6)",{"count":371,"type":20},70,[23],"The number of patients aged over 75 continues to grow, and, according to INSEE, will represent almost 10% of the French population in 2021, an increase of 2.4 points since 2000. This demographic change is also observed in the intensive care units, where admitted patients aged over 80 represent now up to 10-20% of critical care admissions, depending on the facility.\n\nThe admission of these patients remains controversial, with questions about the benefit to elderly patients, both in terms of in-hospital and distant survival, as well as induced morbidity or subsequent quality of life: functional status is impaired in up to two-thirds of survivors.\n\nThe challenge of identifying the patients most able to withstand a stay is a major one. Indeed, a stay in intensive care represents a major stress for the organism, due to the acute condition associated with one or more organ failure(s). Bed rest, immobilization and the use of drugs are responsible for formidable complications in the elderly: muscle-wasting, loss of adaptation to physical effort, loss of autonomy, delirium and agitation, all of which have their own long-term impact.\n\nWhile many studies have looked at the prognostic factors on admission of these patients, and the selection of the patient with the greatest probability of surviving the intensive care unit (ICU), improving the outcome of patients who survive to the ICU stay remains a little-investigated subject. However, the impact of physical and psychological disturbances induced by these patients' stay in intensive care is major, and their detection and management could be elements of interest in improving the care of this population. However, the feasibility of carrying out such an assessment immediately after an ICU stay has yet to be evaluated. The aim of this study would be to evaluate the feasibility of a geriatric assessment at the end of the ICU stay (or within 7 days of discharge) and at 6 months. This study is a prospective, randomized, single-center, open-label interventional study.",[375,27,376,92],"Critical Illness","Older People","2025-04-24",{"date":379,"type":36},"2025-04-29",{"date":381,"type":36},"2024-11-01",{"date":128,"type":20},{"name":384,"class":43},"University Hospital, Strasbourg, France",{"id":386,"slug":387,"hasResults":11,"nctId":388,"briefTitle":389,"officialTitle":389,"acronym":4,"eligibilityCriteria":390,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":391,"targetDuration":4,"studyType":56,"phases":4,"briefSummary":393,"conditions":394,"keywords":4,"overallStatus":123,"whyStopped":4,"lastUpdateSubmitDate":396,"lastUpdatePostDateStruct":397,"startDateStruct":399,"completionDateStruct":401,"leadSponsor":403,"locationsCount":4},"100588312","application-of-the-sg8-scale-in-real-world-geriatric-oncology-patients-100588312","NCT06939764","Application of the sG8 Scale in Real-World Geriatric Oncology Patients","Inclusion Criteria:\n\n1. Patients aged 65 years or older.\n2. Patients with confirmed malignant tumors based on definitive pathological data.\n3. Patients who are assessed by clinicians to have indications for systemic anti-tumor therapy.\n4. Patients with a survival time greater than 12 weeks.\n\nExclusion Criteria:\n\n1. Patients who do not meet the above inclusion criteria or are considered unsuitable for this study by the investigator due to other circumstances.\n2. Patients who are unwilling to cooperate in completing the sG8 scale assessment.\n3. Patients who do not understand the content of this study or are unwilling to participate.",{"count":392,"type":20},346,"This study is a multicenter, prospective, observational study. The study included patients aged 65 and older with solid tumors requiring systemic anti-tumor therapy. All patients underwent screening using the sG8 scale before the start of treatment, followed by routine treatment based on a plan developed through clinician decision-making. The study did not intervene in any way with the patients' diagnosis and treatment, and relevant clinical data during the treatment process were recorded accurately for follow-up patients. Study data were obtained from the electronic medical record databases and hospital information systems of multiple centers, including Sichuan Cancer Hospital. Patient clinicopathological features, pathological diagnoses, clinical stages, previous treatment histories, as well as anti-tumor treatment regimens after patient enrollment, drug dosages per cycle, treatment start times, incidence and grades of adverse events (AEs), and tumor response were extracted and collected from the medical records. All data were entered, managed, quality-controlled, exported, and analyzed through a real-world data management platform (RWDMP).",[395,27],"Solid Cancers","2025-04-15",{"date":398,"type":36},"2025-04-23",{"date":400,"type":20},"2025-05-16",{"date":402,"type":20},"2026-04-30",{"name":404,"class":43},"Sichuan Cancer Hospital and Research Institute",{"id":406,"slug":407,"hasResults":11,"nctId":408,"briefTitle":409,"officialTitle":410,"acronym":4,"eligibilityCriteria":411,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":412,"targetDuration":4,"studyType":56,"phases":4,"briefSummary":413,"conditions":414,"keywords":417,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":419,"lastUpdatePostDateStruct":420,"startDateStruct":422,"completionDateStruct":424,"leadSponsor":425,"locationsCount":44},"100583527","turkish-validation-of-the-geriatric-pain-measure---short-form-100583527","NCT06877481","Turkish Validation of the Geriatric Pain Measure - Short Form","Turkish Adaptation, Validation, and Reliability Assessment of the Geriatric Pain Measure - Short Form","Inclusion Criteria:\n\n* Geriatric patients with chronic pain\n* Patients who agreed to participate in the study\n\nExclusion Criteria:\n\n* Demantia\n* Mental of physical disorders that effect patients answering the scales\n* Diagnosis of malignancy",{"count":194,"type":20},"This study aims to adapt, validate, and assess the reliability of the Geriatric Pain Measure - Short Form in Turkish. A total of 150 patients aged 65 years and older will complete the scale under the supervision of pain management and gerontology specialists. Reliability and validity will be evaluated using statistical analyses, including internal consistency, test-retest reliability, and correlation with validated pain and sleep scales. Ethical approval has been obtained, and all participants will provide informed consent.",[27,415,416],"Pain Measurement","Chronic Pain",[27,415,416,418],"Geriatric Pain Measurement Short Form","2025-03-18",{"date":421,"type":36},"2025-03-20",{"date":423,"type":36},"2025-03-15",{"date":284,"type":20},{"name":426,"class":75},"Başakşehir Çam & Sakura City Hospital",{"id":428,"slug":429,"hasResults":11,"nctId":430,"briefTitle":431,"officialTitle":432,"acronym":433,"eligibilityCriteria":434,"healthyVolunteers":11,"sex":16,"minAge":53,"maxAge":4,"enrollmentInfo":435,"targetDuration":4,"studyType":56,"phases":4,"briefSummary":436,"conditions":437,"keywords":4,"overallStatus":123,"whyStopped":4,"lastUpdateSubmitDate":439,"lastUpdatePostDateStruct":440,"startDateStruct":442,"completionDateStruct":444,"leadSponsor":446,"locationsCount":44},"100583253","a-geriatric-mobile-team-for-nursing-home-residents-a-feasibility-pilot-study-100583253","NCT06873919","A Geriatric Mobile Team for Nursing Home Residents: a Feasibility Pilot Study","A Geriatric Mobile Team for Nursing Home Residents: an Exploratory, Prospective, Single-Center, Non-Randomized, Non-Interventional Feasibility Pilot Study","GerMoT","Inclusion Criteria:\n\n* Patients aged over 70 years\n* Presenting with one or more of the following conditions:\n\n  * Difficulties in establishing an advance care planning\n  * Medical complexity (multiple specialists, repeated hospitalizations)\n  * Polypharmacy\n  * Recurrent falls\n  * Unmanageable behavioral disorders\n  * Weight loss\n  * Memory impairment\n\nExclusion Criteria:\n\n* Patients with an unstable medical condition requiring urgent care\n* Patients under 70 years old\n* Patients whose condition requires examinations or treatments available only in a hospital setting",{"count":55,"type":20},"Nursing home (NH) residents have complex healthcare needs. Barriers to collaboration hinder the delivery of high-quality care in nursing homes. To bridge the gap between hospital-based and NH-based care, various innovative approaches have been proposed, including geriatric mobile teams. In Belgium, geriatric expertise has long been confined to hospital settings. Until recently, no specific organization existed for outpatient geriatric assessment, particularly for NH residents. In April 2024, the National Institute for Health and Disability Insurance (INAMI) introduced a new reimbursement code for geriatric consultations in NHs, promoting the development of extramural geriatric activities. However, evidence on the effectiveness of mobile geriatric teams remains limited, particularly regarding hospitalization prevention.\n\nThe geriatrics department of CHU UCL Namur is implementing a one-year pilot project involving a mobile team composed of a geriatrician and a nurse to conduct geriatric assessments in the three nursing homes. This non-randomized pilot project aims to establish a new standard of care for residents selected by their general practitioner, leveraging the new reimbursement code. The project is accompanied by a clinical study assessing the feasibility, effectiveness, and acceptability of this intervention. Prospectively collected data will also help define key indicators for a future large-scale study focused on cost-effectiveness.",[438,27],"Nursing Home Resident","2025-03-10",{"date":441,"type":36},"2025-03-13",{"date":443,"type":20},"2025-03-05",{"date":445,"type":20},"2026-02-28",{"name":447,"class":43},"Université Catholique de Louvain",{"id":449,"slug":450,"hasResults":11,"nctId":451,"briefTitle":452,"officialTitle":453,"acronym":4,"eligibilityCriteria":454,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":455,"targetDuration":4,"studyType":21,"phases":457,"briefSummary":458,"conditions":459,"keywords":461,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":472,"lastUpdatePostDateStruct":473,"startDateStruct":475,"completionDateStruct":477,"leadSponsor":479,"locationsCount":44},"100566220","understanding-the-preferences-and-views-of-older-adults-on-the-use-of-geriatric-and-objective-functional-assessments-for-cancer-treatment-planning-100566220","NCT06652347","Understanding the Preferences and Views of Older Adults on the Use of Geriatric and Objective Functional Assessments for Cancer Treatment Planning.","Facilitating the Engagement and Satisfaction of Older Adults in Their Cancer Care Planning: A Randomized Study to Understand the Preferences and Views of Older Adults Regarding the Use of Geriatric and Objective Functional Assessments for Cancer Treatment Planning","Inclusion Criteria:\n\n* Age ≥ 65\n\nAt the time of study screening either:\n\n* Started a new qualifying index regimen within the last 30 days (inclusive)\n* Are being considered for a new qualifying index regimen\n\nExclusion Criteria:\n\n* Patients will be excluded if they\n\n  * Do not have the capacity to consent to study procedures\n  * Are unable to complete English language questionnaires\n  * Are already using an activity tracker on a daily basis (and therefore may be aware of their current level of activity)\n  * Are enrolled in another study in which physical activity is a substantial part or all of the therapeutic intervention or where physical activity is specifically being evaluated and shared with patients. Patients on studies not evaluating or sharing physical activity are eligible for the present study if they meet the other inclusion\u002Fexclusion criteria and participation in the present study is not excluded by other studies in which they are enrolled.",{"count":456,"type":20},100,[23],"This Interventional clinical study aims to explore how receiving information about their health and physical abilities affects the treatment decisions of older adults. The study will look at whether sharing detailed assessments of their health and functional status helps older adults better understand their condition and make informed decisions about their care.\n\nThe main question it aims to answer is if providing this information changes the treatment priorities of older adults, helping them focus on what matters most to them in their medical care.",[460,203,27],"Care Delivery",[462,463,464,465,466,467,468,469,470,471],"fitness tracking","Care delivery Intervention","Functional Status in Older Adults","Cancer Treatment Preferences","Quality vs Quantity of Life","Patient-Reported Outcomes in Oncology","Randomized Controlled Trial","Quality of Life in Cancer care","Functional Health Assessments","Patient-Centered Cancer Treatment","2025-02-25",{"date":474,"type":36},"2025-02-27",{"date":476,"type":36},"2025-02-21",{"date":478,"type":20},"2026-11",{"name":480,"class":43},"Fox Chase Cancer Center",{"id":482,"slug":483,"hasResults":11,"nctId":484,"briefTitle":485,"officialTitle":486,"acronym":4,"eligibilityCriteria":487,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":488,"targetDuration":4,"studyType":21,"phases":490,"briefSummary":491,"conditions":492,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":499,"lastUpdatePostDateStruct":500,"startDateStruct":502,"completionDateStruct":504,"leadSponsor":506,"locationsCount":44},"100369604","optimized-recovery-after-trauma-in-geriatric-patient-100369604","NCT04092504","Optimized Recovery After Trauma in Geriatric Patient","Optimized Recovery After Trauma in Geriatric Patient (Gero - ERAT)","Inclusion Criteria:\n\n* ≥ 65 years old\n* In hospital due to physical trauma\n* Able to speak and understand Swedish\n\nExclusion Criteria:\n\n* Documented palliative care\n* Cognitive impairment",{"count":489,"type":20},540,[23],"Currently, there is evidence that structured care within the healthcare system increases the conditions for good care and better recovery. We want to investigate whether a new care concept (gero-ERAT) that combines two variants of structured care can improve the recovery of elderly patients affected by a physical trauma.\n\nOur hope is that the project will reduce the complications, short care times, fewer re-admissions and that more patients can return to regular living, which reduces the suffering for the patient and his relatives. In addition to patient benefit, a successful outcome will also result in reduced costs for healthcare and society as a whole. The concept of care is based on an increased patient participation, which is in line with the values of the Västra Götaland region and the Sahlgrenska university hospital\n\nThrough the PhD project, four studies will be published. A qualitative interview study to investigate patients' experiences of care and recovery after trauma.\n\nAfter that, a prospective cohort survey of two groups is carried out; conventional care and gero-ERAT. Data will begin to be collected in the control group and when the control group is full geroRATAT will be implemented in the care department and we then collect data in the intervention group.\n\nBased on collected data, we will publish two additional studies one with a focus on health economics as well as one focusing on care time and recovery based on age and harvest estimation.",[27,493,494,495,496,497,498],"Quality of Life","Trauma","Fragility","Injury","Rehabilitation","Recovery","2024-11-21",{"date":501,"type":36},"2024-11-25",{"date":503,"type":36},"2019-05-09",{"date":505,"type":20},"2028-01-01",{"name":507,"class":75},"Vastra Gotaland Region",{"id":509,"slug":510,"hasResults":11,"nctId":511,"briefTitle":512,"officialTitle":513,"acronym":514,"eligibilityCriteria":515,"healthyVolunteers":11,"sex":16,"minAge":53,"maxAge":4,"enrollmentInfo":516,"targetDuration":4,"studyType":21,"phases":518,"briefSummary":519,"conditions":520,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":522,"lastUpdatePostDateStruct":523,"startDateStruct":525,"completionDateStruct":527,"leadSponsor":529,"locationsCount":183},"100504461","functional-status-and-quality-of-life-in-older-patients-undergoing-robotic-surgery-for-colorectal-cancer-100504461","NCT05848609","Functional Status and Quality of Life in Older Patients Undergoing Robotic Surgery for Colorectal Cancer","Prospective Evaluation of Functional Status and Quality of Life in Older Patients With Colorectal Cancer Undergoing Robotic Surgery","ROBO-G","Inclusion Criteria:\n\n* patients ≥ 70 years with colorectal cancer\n* eligible for colorectal surgery after multidisciplinary board evaluation and patient consent\n\nExclusion Criteria:\n\n* decline in cognitive function after geriatric evaluation\n* emergency surgery\n* life expectancy \\\u003C 3 months",{"count":517,"type":20},120,[23],"The present study evaluates prospectively the impact of robotic surgery on functional outcome and quality of life in older patients that are operated for colorectal cancer;",[521,27,493],"Colorectal Surgery","2023-04-28",{"date":524,"type":36},"2023-05-08",{"date":526,"type":36},"2023-03-15",{"date":528,"type":20},"2026-12-31",{"name":530,"class":43},"Universitair Ziekenhuis Brussel"]