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Efficacy and Implementation Potential of an AR-Guided Exercise Program for Community-Dwelling Older Adults with Frailty: A Quasi-Experimental Study

Efficacy and Implementation Potential of an Exergaming on Community-Dwelling Older Adults with Frailty: A Quasi-Experimental Study

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400087541
Enrollment
Unknown
Registered
2024-07-30
Start date
2024-07-31
Completion date
Unknown
Last updated
2025-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

frailty

Interventions

Intervention group:Participants in the experimental group will receive a 12-week AR-guide home-based exergame programme by using the Nintendo SwitchTM console (Switch, Nintendo, Kyoto, Japan) and the
Control group:Participants will practice elastic band exercises twice on two non-consecutive days each week for 12 weeks

Sponsors

Xiangya School of Nursing
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 100 Years

Inclusion criteria

Inclusion criteria: (1) aged >=60; (2) living at home with a TV; (3) having frailty (GFI score >=3); (4) mentally competent (Abbreviated Mental Test (AMT) score >=7); (5) able to speak and understand Mandarin.

Exclusion criteria

Exclusion criteria: (1) have several visual impairments which affect the implementation of exergame; (2) life expectancy of fewer than six months or diagnosis of terminal illness; (3) are currently participating in exercise for at least 150 minutes per week; (4) are currently participating in any other trial; (5) undergone or will undergo major surgery in the past six months or in the coming six months, respectively; (6) are receiving active psychiatric or antidepressant treatment; (7) have conditions which contraindicate to physical exercise practice according to ViviFrail Programme which has been widely used in practising exercise in older people with frailty. (Acute myocardial infarction or recent unstable angina, uncontrolled atrial or ventricular arrhythmias, dissecting aortic aneurysm, severe aortic stenosis, endocarditis / acute pericarditis, uncontrolled high blood pressure, acute thromboembolic disease, acute or severe heart failure, acute or severe respiratory failure, uncontrolled postural hypotension, acute decompensated diabetes mellitus or uncontrolled low blood sugar, a recent fracture in the last month)

Design outcomes

Primary

MeasureTime frame
Adherence rate;Participation rate;Attrition rate;Frailty level;Satisfaction level;

Secondary

MeasureTime frame
Depressive symptoms;Anxiety;Loneliness;Quality of life;Social support;Physical functions;

Countries

China

Contacts

Public ContactLi Liu; Zhige Yan

Xiangya School of Nursing, Central South University

liuli26@csu.edu.cn+86 147 8996 6445

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026