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A Individualized Physical Function Improvement Program for Frailty Elderly Using Goal Attainment Scaling (GAS) as Evaluation Method: Protocol for a Randomized Controlled Trial

Capital Medical University logo

Capital Medical University

Status

Not yet enrolling

Conditions

Elderly

Treatments

Combination Product: Multicomponent frailty intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT06919575
CYYY-Frailty-GAS

Details and patient eligibility

About

Frailty refers to the age-related decline in physiological functions,that is associated with adverse outcomes. Frailty is a dynamic reversible state, that requires a comprehensive individualized management. Goal Attainment Scaling (GAS) is a structured, individualized method for setting and evaluating progress toward personalized goals.

We conducted a randomized clinical trial of an individualized intervention program using GAS as evaluation method designed to improve physical functional in frailty elderly. A total of 160 individuals aged ≥60 years, who fulfill the Fried scale of frailty will be recruited from Beijing Chaoyang Hospital, Capital Medical University. All participants set personalized goals through GAS. Patients in the intervention group receive individualized interventions, implement tailored measures based on personalized goals to reverse the frailty state.The participants will be followed-up for 3 months and 24 months.

This protocol would be established to examine the efficiency of targeted individualized intervention for frailty based on the GAS. If a positive consequence could be obtained, the results of this study will provide critical data for management of frailty in the elderly, that can be carried out in routine clinical practice.

Enrollment

160 estimated patients

Sex

All

Ages

60+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

The inclusion criteria were the following: (1)≥60-years old; (2) recognized as frailty by Fried scale.

The exclusion criteria were the following: (1) considered with life expectancy < 1 year such as advanced cancer patients; (2) difficult to communicate with such as patients with severe cognitive impairment (Mini Mental State Examination score ≤ 17); (3) severe hearing disord.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

Triple Blind

160 participants in 2 patient groups

the intervention group
Experimental group
Description:
the intervention group will receive individualized interventions.
Treatment:
Combination Product: Multicomponent frailty intervention
The control group
No Intervention group
Description:
The control group will receive routine diagnosis and treatment

Trial contacts and locations

0

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Central trial contact

xiaojuan Wang, PHD

Data sourced from clinicaltrials.gov

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