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Effects of a 12-week Tai Chi program on physical function, lung function, pain, depression, and quality of life among older people living in the aged care homes: A feasibility study

Effects of a 12-week Tai Chi program on physical function, lung function, pain, depression, and quality of life among older people living in the aged care homes: A feasibility study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
SLCTR
Registry ID
SLCTR/2025/025
Enrollment
40
Registered
2025-06-26
Start date
2025-07-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Older adult health

Interventions

The study will be carried out in aged care homes in the Kandy district, Sri Lanka. Aged care homes will be purposively selected based on the number of participants who are willing to participate in th

Sponsors

University of Peradeniya
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. All residents aged 60 and above living in the selected aged care homes 2. Both males and females

Exclusion criteria

Exclusion criteria: 1. Score of 18 or above on the Sinhala Version of the Mini-Mental State Examination (MMSE) 2. Presence of any diagnosed disorders of the central nervous system or neurodegenerative diseases such as Parkinson Disease, Huntington’s disease and Amyotrophic Lateral Sclerosis, as determined by medical records. 3. Diagnosis of depression or dementia as determined by medical records 4. Any orthopedic or cardiovascular disorders that impede ambulatory function or the ability to stand. 5. Severe hearing impairment that inhibits the ability to follow evaluation instructions and therapist guidance. 6. Severe visual impairment that affects the individual’s safety during the execution of exercises. 7. Any history of lower-limb fractures in the preceding 6 months. 8. Prior experience in Tai-Chi exercise for more than 2 months

Design outcomes

Primary

MeasureTime frame
Physical function through 1. Grip strength in both hands will be assessed with a digital hand dynamometer (0-90 kg; Labisen KS-301). For each hand, the higher score of the two repeated measurements will be recorded. 2 Balance: The one-leg-standing balance test (OLST) 3. Flexibility assessment of the lower body will be assessed by the Chair Sit and Reach Test (CSR). 4. Mobility as assessed by the timed Up and Go test (TUG) [Baseline and at the end of the 12 weeks ] Lung function: Spirometry will be used to assess lung functions using a standard protocol. Parameters will include Forced Expiratory Volume in one second (FEV1), percentage predicted Forced Vital Capacity (%FVC), and FEV1 percentage predicted normal values (FEV1%). [ Baseline and at the end of the 12 weeks] Pain will be assessed by the Numeric Rating Scale (NRS). Any physical pain during the past 24 hours will be considered. [ Baseline and at the end of the 12 weeks] Depressive symptoms will be assessed using the Sinhala Version of Geriatric Depression Scale (GDS) Short Form. [ Baseline and at the end of the 12 weeks] Quality of Life will be assessed by the Sinhala Version of Euro Quality of Life Questionnaire (EQ5D). [ Baseline and at the end of the 12 weeks]

Secondary

MeasureTime frame
1. Feasibility - Assesed based on acceptability, demand, implementation, practicality, adaptation, integration, expansion, study limitation and limited efficacy testing. [At the end of the 12 weeks]

Countries

Sri Lanka

Contacts

Public ContactE.M.J.S.K. Ekanayaka

Senior Lecturer (Grade II)

sanya@ahs.pdn.ac.lk0702566515

Outcome results

None listed

Source: SLCTR (via WHO ICTRP) · Data processed: Aug 10, 2026