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Clinical Trials/NCT07831356
NCT07831356CompletedNot Applicable

The Effect Of Tai Chi On Quality Of Life And Depression In Elderly Patients With Sarcopenia : A Randomized Controlled Trial

Hasanuddin University1 site in 1 country40 target enrollmentStarted: January 24, 2026Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
40
Locations
1
Primary Endpoint
Sarcopenia Quality of Life (SarQoL) questionnaire

Study Overview

Brief Summary

This study aims to evaluate the effects of Tai Chi exercise on quality of life and depressive symptoms in elderly with sarcopenia. Sarcopenia is characterized by a progressive decline in skeletal muscle mass and muscle strength, which may contribute to impaired physical function, reduced quality of life, and an increased risk of adverse health outcomes among older adults. Specifically, this study investigates the effects of an eight-week Tai Chi exercise program on health-related quality of life, assessed using the Sarcopenia Quality of Life (SarQoL) questionnaire, and depressive symptoms, assessed using the Geriatric Depression Scale-15 (GDS-15), in elderly individuals diagnosed with sarcopenia.

The primary research question of this study is whether an eight-week Tai Chi exercise program can improve quality of life and reduce depressive symptoms in elderly individuals with sarcopenia. Furthermore, this study aims to determine whether Tai Chi exercise results in greater improvements in SarQoL scores and GDS-15 scores compared with a control group participating in standard elderly exercise.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Triple (Participant, Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
60 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Aged 60 years or older
  • Meets the diagnostic criteria for sarcopenia based on the Asian Working Group for Sarcopenia (AWGS).
  • Willing to participate in the study, capable of understanding the informed consent, and physically able to perform Tai Chi movements.
  • Must be a resident of Makassar.
  • Has either never participated in Tai Chi, or has previous experience with Tai Chi but stopped practicing for more than 4 weeks (ensuring they are not currently active practitioners).

Exclusion Criteria

  • Cognitive impairment, indicated by a Mini-Mental State Examination (MMSE) score of 23 or lower.
  • Hearing and/or speech impairments that make communication difficult. Presence of severe chronic diseases, such as heart failure, end-stage chronic kidney disease, malignancy, or the use of a pacemaker.
  • Presence of edema (fluid retention/swelling).
  • Experiencing lower extremity (leg) pain with a Visual Analogue Scale (VAS) score of 5 or greater.

Arms & Interventions

Tai Chi Exercise Group

Experimental

Elderly participants diagnosed with sarcopenia who are randomly assigned to participate in a supervised Tai Chi exercise program.

Intervention: Tai Chi Exercise (Behavioral)

Elderly Exercise (Senam Lansia) Group

Active Comparator

Elderly participants diagnosed with sarcopenia who are randomly assigned to participate in a standard elderly exercise program

Intervention: Elderly exercise (senam lansia) (Behavioral)

Outcomes

Primary Outcomes

Sarcopenia Quality of Life (SarQoL) questionnaire

Time Frame: Baseline (Week 0) and post-intervention (Week 8)

This outcome measures health-related quality of life in older adults with sarcopenia using the Sarcopenia Quality of Life (SarQoL) questionnaire. The SarQoL questionnaire consists of 55 items covering seven domains: physical and mental health, locomotion, body composition, functionality, activities of daily living, leisure activities, and fears. The questionnaire generates a total SarQoL index score ranging from 0 to 100, with higher scores indicating better sarcopenia-related quality of life. The validated scoring algorithm is used to calculate the overall SarQoL index score.

Geriatric Depression Scale-15 (GDS-15)

Time Frame: Baseline (Week 0) and post-intervention (Week 8)

This outcome measures depressive symptoms in older adults using the 15-item Geriatric Depression Scale (GDS-15). Each item is answered with a yes/no response and scored according to the established scoring criteria, with a total score ranging from 0 to 15. Higher scores indicate a greater severity of depressive symptoms. The GDS-15 is used to assess changes in depressive symptoms following the eight-week intervention.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Hasanuddin University
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Dea Mardia Rauf

Resident of Physical Medicine and Rehabilitation Faculty of Medicine Hasanuddin University

Hasanuddin University

Study Sites (1)

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