[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"frail-elderly-patients\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:frail-elderly-patients":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,49,81],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":30,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":48},"100640551","improving-care-for-frail-older-adults-using-a-digital-needs-assessment-tool-100640551",false,"NCT07580690","Improving Care for Frail Older Adults Using a Digital Needs Assessment Tool","Integrating Health and Social Service Needs for Frail Elders at Point of Care: Development and Evaluation of an IT-based Digital Needs-assessment Tool","Frailty","Inclusion Criteria:\n\n* Patient participant: (i) Aged \\>= 60 years at the time of recruitment; (ii) identified as frail, with a CFS score \\>= 5 and\u002For modified HFRS intermediate and high frailty risk (mHFRS) score \\>=5; (iii) Singapore citizens or permanent residents; (iv) able to speak and understand English, Chinese or Malay.\n* Proxy (when responding on behalf of eligible patients): (i) Relative or friend of the patient participant; (ii) Aged 21 years or older; (iii) Familiar with the older adult's health and social situation.\n\nExclusion Criteria:\n\n* Patient participant: (i) Currently involved in another study or (ii) residents of nursing homes, or (iii) patients known to home hospice or home palliative care services with a life expectancy of less than 6 months.\n* Proxy: primary caregivers who are foreign domestic workers will be excluded from the study.","ALL","60 Years",{"count":20,"type":21},200,"ESTIMATED","INTERVENTIONAL",[24],"NA","The goal of this trial is to evaluate whether a digital needs-assessment tool can improve care planning and outcomes for frail older adults (aged 60 years and above) hospitalized in Singapore. The tool is designed to identify patients' health and social service needs and support better care coordination after hospital discharge.\n\nThe main questions it aims to answer are:\n\n* Does the use of a digital needs-assessment tool improve the identification and management of health and social service needs in frail older adults?\n* Does this approach improve patient outcomes, such as quality of life, care satisfaction, and healthcare utilization after discharge?\n\nParticipants will:\n\n* Respond to a baseline questionnaire\n* Receive a personalized care plan based on identified needs by the tool\n* Be followed up at 1 month and 3 months after discharge through surveys\n* Some participants will receive additional follow-up phone calls to review care needs and service use\n* A subset of participants will take part in interviews to share their care experiences",[27,28,29],"Frail Elderly Patients","Geriatric Syndromes","Frail Older Adults",[29,31,32,33,34,35],"Simple Segmentation Tool","Integrated Care","Care Coordination","Needs Assessment Tool","Health and Health-related Social Service","NOT_YET_RECRUITING","2026-05-05",{"date":39,"type":40},"2026-05-12","ACTUAL",{"date":42,"type":21},"2026-05-01",{"date":44,"type":21},"2027-12-30",{"name":46,"class":47},"Duke-NUS Graduate Medical School","OTHER",1,{"id":50,"slug":51,"hasResults":11,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":4,"eligibilityCriteria":55,"healthyVolunteers":11,"sex":56,"minAge":57,"maxAge":4,"enrollmentInfo":58,"targetDuration":4,"studyType":22,"phases":60,"briefSummary":62,"conditions":63,"keywords":67,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":48},"100632333","phase-2-effect-of-testosterone-on-elderly-frail-men-with-testosterone-deficiency-100632333","NCT07512323","Effect of Testosterone on Elderly Frail Men With Testosterone Deficiency","Effect of Testosterone on Elderly Frail Men With Testosterone Deficiency - a Double-blinded, Randomized and Placebo-controlled Intervention Study","Inclusion Criteria:\n\n* Men aged 70 or over.\n* Living at home in their own home or in sheltered housing.\n* Independent walking function, possibly with a walking aid.\n* Able to perform the chair-stand test a maximum of 8 times in 30 seconds or Timed Up and Go (TUG) of at least 30 seconds.\n* There must be at least 3 symptoms of frailty or objective findings.\n* Serum testosterone \\\u003C 10 nmol\u002FL as an average of 2 independent measurements at the Center for Growth and Reproduction, Rigshospitalet.\n\nExclusion Criteria:\n\n* Known or previous prostate cancer.\n* Abnormally elevated serum PSA (PSA = prostate-specific antigen) corresponding to PSA \\> 5 ng\u002Fml or PSA \\> 0.15 ng\u002Fml\u002Fcc (relative to prostate size in cubic centimeters (cc)).\n* Hemochromatosis.\n* Heart diseases in the form of: Peri-, myo-, or endocarditis, angina pectoris, severe heart failure (NYHA class III and IV), severe hypertension (systolic BP \\> 180 or diastolic BP \\> 105 mmHg after possible antihypertensive treatment). - Resting dyspnea.\n* Liver (ASAT \\> 2 x upper normal limit) or renal insufficiency (serum creatinine \\> 200 micromol\u002Fl).\n* Severe intractable epilepsy or migraine.\n* Insulin treatment.\n* Previous or current bisphosphonate, fluoride, HRT, SERM, strontium, teriparatide, or more than 3 weeks of prednisolone treatment.\n* Joint disease with acute inflammation.\n* Active cancer disease, in chemo- or radiotherapy.\n* Bone metabolic disease except for age-related osteoporosis.\n* Autoimmune diseases, chronic systemic diseases (cirrhosis, AIDS, chronic renal failure).\n* Primary testosterone deficiency in the form of testicular dysgenesis, Klinefelter syndrome (47,XXY), 46,XX males, LH resistance, Y chromosome deletions, other sex chromosome abnormalities.\n* Significant abuse, mental illness, dementia, physical handicaps with inability to complete the intervention or tests, or to give informed consent.\n* Contraindications for testosterone undecanoate are thus included in exclusion criteria, such as the presence of liver tumors, breast carcinoma, and prostate cancer, for which trial participants will be examined before the start of the trial.","MALE","70 Years",{"count":59,"type":21},96,[61],"PHASE2","The purpose of this study is to increase the functional level of the elderly to thereby reduce fall risk, improve motor skills, and increase psychological well-being, as well as to assess whether the restoration of a normal testosterone level contributes to a faster recovery. The effect of testosterone is investigated as measured by physical and mental functional capacity, including cognition, in hypogonadal elderly men with a significant loss of function. The study is aimed at participants who are too weak to participate in the progressive strength training.",[27,64,65,66],"Hypogonadal Males","Testosterone Replacement Therapy","Falls (Accidents) in Old Age",[68,69,70,71],"hypogonadism","frailty","falls","testosterone replacement therapy","2026-04-29",{"date":74,"type":40},"2026-05-06",{"date":76,"type":21},"2026-08-01",{"date":78,"type":21},"2030-09-30",{"name":80,"class":47},"Rune Skovgaard Rasmussen",{"id":82,"slug":83,"hasResults":11,"nctId":84,"briefTitle":85,"officialTitle":85,"acronym":4,"eligibilityCriteria":86,"healthyVolunteers":11,"sex":17,"minAge":87,"maxAge":4,"enrollmentInfo":88,"targetDuration":4,"studyType":22,"phases":90,"briefSummary":91,"conditions":92,"keywords":93,"overallStatus":95,"whyStopped":4,"lastUpdateSubmitDate":96,"lastUpdatePostDateStruct":97,"startDateStruct":99,"completionDateStruct":101,"leadSponsor":103,"locationsCount":48},"100603470","a-multicenter-observational-study-of-an-integrated-traditional-chinese-and-western-medicine-care-model-in-post-acute-treatment-of-frail-elderly-patients-100603470","NCT07136935","A Multicenter Observational Study of an Integrated Traditional Chinese and Western Medicine Care Model in Post-Acute Treatment of Frail Elderly Patients","Inclusion Criteria:\n\n1. Elderly patients aged ≥75 years.\n2. A history of at least one of the following conditions: Parkinson's disease, chronic obstructive pulmonary disease (COPD), mild dementia, or chronic kidney disease at stage 3 or above.\n3. Hospitalized due to an acute illness (length of hospital stay \\>72 hours).\n4. Functional decline within one month after completion of treatment.\n5. Clinical Frailty Scale (CFS) score of 5-7 (indicating moderate or greater frailty, with retained rehabilitation potential).\n6. Can answer clinical questionnaires and scales.\n\nExclusion Criteria:\n\n1. Medically unstable (requiring intensive medical interventions, diagnostic testing, or supplemental oxygen).\n2. Unable to cooperate with treatment or communication.","20 Years",{"count":89,"type":21},20,[24],"Exploring the Impact and Effectiveness of an Integrated Traditional Chinese and Western Medicine Treatment Model in Post-Acute Care for Frail Older Patients.",[27],[69,94],"Chinese and Western Integrated medicine","RECRUITING","2025-08-21",{"date":98,"type":40},"2025-08-22",{"date":100,"type":40},"2025-07-28",{"date":102,"type":21},"2027-03-31",{"name":104,"class":47},"China Medical University Hospital"]