[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Hangzhou Normal University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":71},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,44],{"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":28,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":43},"100643264","bcw-based-resistance-training-for-community-dwelling-sarcopenia-patients-100643264",false,"NCT07601321","BCW-Based Resistance Training for Community-Dwelling Sarcopenia Patients","Effects of a Behavior Change Wheel (BCW)-Based Resistance Exercise Program on Community-Dwelling Patients With Sarcopenia: A Randomized Controlled Trial","BCW-RES","Inclusion Criteria:\n\nMeet the diagnostic criteria for sarcopenia according to the Asian Working Group for Sarcopenia (AWGS) 2025:\n\nLow muscle mass (SMI measured by BIA): For age ≥ 65, Male \\\u003C 7.0 kg\u002Fm², Female \\\u003C 5.7 kg\u002Fm²; For age 50-64, Male \\\u003C 7.6 kg\u002Fm², Female \\\u003C 5.7 kg\u002Fm².\n\nLow muscle strength (Handgrip strength): For age ≥ 65, Male \\\u003C 28 kg, Female \\\u003C 18 kg; For age 50-64, Male \\\u003C 34 kg, Female \\\u003C 20 kg.\n\nAbility to walk independently without assistive devices.\n\nClear consciousness and stable medical condition.\n\nWillingness to participate, commit to the exercise protocol, and provide signed informed consent.\n\nProficiency in using a smartphone.\n\nExclusion Criteria:\n\n* Presence of metal implants, such as cardiac pacemakers, stents, steel plates, or artificial joints (due to BIA measurement constraints).\n\nCognitive impairment, epilepsy, other neurological disorders, or severe mental illness that prevents cooperation with the study.\n\nInability to complete the exercise intervention due to severe cardiovascular or musculoskeletal diseases.\n\nSevere organ dysfunction (e.g., heart failure), organ failure, or active infection.\n\nInability to maintain adherence or significant missing data (participants who withdraw or are lost to follow-up).","ALL","50 Years",{"count":20,"type":21},100,"ESTIMATED","INTERVENTIONAL",[24],"NA","The purpose of this randomized controlled trial is to evaluate the effects of a Behavior Change Wheel (BCW)-based resistance exercise program on muscle health, physical performance, and exercise adherence in community-dwelling older adults with sarcopenia. Participants will be randomly assigned to either an experimental group or a waitlist control group. The experimental group will receive a 12-week BCW-based resistance exercise intervention (twice a week) immediately. The waitlist control group will maintain their usual routine for the first 3 months for comparison, and will then cross over to receive the identical 12-week intervention. The study aims to provide an effective and ethical exercise management strategy for sarcopenic patients.",[27],"Sarcopenia",[27,29,30],"Resistance Exercise","Behavior Change Wheel","NOT_YET_RECRUITING","2026-06-08",{"date":34,"type":35},"2026-06-10","ACTUAL",{"date":37,"type":21},"2026-06",{"date":39,"type":21},"2026-12",{"name":41,"class":42},"Hangzhou Normal University","OTHER",1,{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":49,"acronym":4,"eligibilityCriteria":50,"healthyVolunteers":51,"sex":17,"minAge":52,"maxAge":4,"enrollmentInfo":53,"targetDuration":4,"studyType":22,"phases":55,"briefSummary":56,"conditions":57,"keywords":59,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":63,"lastUpdatePostDateStruct":64,"startDateStruct":66,"completionDateStruct":68,"leadSponsor":70,"locationsCount":43},"100557351","effect-of-an-oral-frailty-measures-intervention-programs-in-institutionalized-elders-100557351","NCT06536985","Effect of an Oral Frailty Measures Intervention Programs in Institutionalized Elders","Effect of an Oral Frailty Measures Program in Institutionalized Elders: a Study Protocol of a Cluster-Randomized Controlled Trial","Inclusion Criteria:\n\n1. Age ≥ 65 years old\n2. Residing in a nursing home for ≥ 3 months\n3. Meeting at least three of the six criteria for oral frailty\n4. Conscious and with normal reading and comprehension abilities\n5. Informed consent to participate in this study\n\nExclusion Criteria:\n\n1. Edentulous state without dentures\n2. Cognitive or communication impairments\n3. Elderly lacking self-care ability",true,"65 Years",{"count":54,"type":21},226,[24],"This is a compelling 16-week prospective, double-blind, whole-cluster randomized controlled trial(RCT).This study will recruit 226 older adults over the age of 65.Based on King's goal attainment theory, a program to promote oral health is developed.The study aims to evaluate the effectiveness of a mixed face-to-face and eHealth oral health promotion program for older adults with oral frailty in nursing homes, based on the Theory of Planned Behavior.",[58],"Frailty",[60,61,62],"Nursing Homes","Aged","Exercise","2024-10-30",{"date":65,"type":35},"2024-11-04",{"date":67,"type":21},"2024-11-11",{"date":69,"type":21},"2025-11-11",{"name":41,"class":42},""]