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Construction and evaluation of frailty intervention strategies for older adults in the community: a type II hybrid effectiveness-implementation study.

Construction and evaluation of frailty intervention strategies for older adults in the community: a type II hybrid effectiveness-implementation study.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300070392
Enrollment
Unknown
Registered
2023-04-11
Start date
2023-04-16
Completion date
Unknown
Last updated
2023-06-04

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

Conditions

Frail

Interventions

1:Feedback+Goal setting+Intensive guidance+Core intervention
2:Feedback+Goal setting+Core intervention
3:Feedback+Intensive guidance+Core intervention
4:Goal setting+Intensive guidance+Core intervention
5:Feedback+Core intervention
6:Goal setting+Core intervention
7:Intensive guidance+Core intervention
8:Core interventions (control)

Sponsors

Xiangya School of Public Health, Central South University.
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 90 Years

Inclusion criteria

Inclusion criteria: (1) Age = 60 years and able to walk to the community health centre on their own; (2) debilitation assessed using the Fried debilitation phenotype with a score = 1. (3) existing exercise not meeting WHO recommendations of 150-300 minutes of aerobic exercise per week or 75-150 minutes of resistance training per week or a mixture of resistance and aerobic exercise; (4) participants gave informed consent, volunteered to participate and signed consent form.

Exclusion criteria

Exclusion criteria: (1) at potential risk of physical activity (meeting any of the Physical Activity Risk Assessment Scale PAR-Q) (2) have terminal disease with an expected survival of = 12 months; (3) have dementia or severe cognitive impairment; (4) have a history of Parkinson's disease and Parkinson's syndrome, epilepsy, malignancy, etc.; (5) have severe functional deficits in vision, hearing and comprehension; (6) have severe mental illness; (7) are already enrolled in other intervention programmes.

Design outcomes

Primary

MeasureTime frame
Frail;Adherence;

Secondary

MeasureTime frame
Muscle mass;Physical functions;Quality of life;Acceptability;Appropriateness;Feasibility;Organizational Readiness for Implementing Change;Organizational Readiness for Implementing Change;Intervention costs;

Countries

China

Contacts

Public ContactXinyin Wu

Central South University

irenexywu@csu.edu.cn18390825035

Outcome results

None listed

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