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Tai Chi Interventions on Physical Functions Among Older Adults

Feasibility and Effectiveness of a Multimodal Exercise Intervention on Physical Activity and Physical Functions in Low-Income Older Adults

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07228169
Enrollment
27
Registered
2025-11-14
Start date
2025-02-27
Completion date
2025-09-23
Last updated
2025-11-14

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

Conditions

Combined Multicomponent Exercise and Tai Chi

Keywords

Multicomponent exercise, Tai Chi, Physical activity, Physical function

Brief summary

This study examined the feasibility and effectiveness of a multimodal exercise intervention on an objective measure of physical activity (PA), and objective and subjective measures of physical functions among older adults living in a low-income senior housing complex.

Detailed description

This study aimed to examine the feasibility and effectiveness of a multimodal exercise intervention on an objective measure of physical activity (PA), and objective and subjective measures of physical functions among older adults living in a low-income senior housing complex. 23 older adults (mean age = 80.17 ± 6.913 years) residing in a low-income senior housing complex voluntarily participated in an 8-week intervention. The feasibility of the study was assessed throughout the study period. Additionally, participants completed The Acceptability, Appropriateness, and Feasibility of the Intervention Questionnaire (AAF-IQ) after the intervention. The study outcomes, including physical activity and physical functions, were measured within two weeks before and after the intervention.

Interventions

BEHAVIORALCombined multicomponent exercise and Tai Chi

The combined multicomponent exercise and Tai Chi intervention includes that participants attended one 45-minute multicomponent exercise group session and one 45-minute Tai Chi group sessions along with self-practice each week, for eight weeks.

Sponsors

University of Michigan
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Intervention model description

Participants attended one 45-minute multicomponent exercise group session and one 45-minute Tai Chi group session each week for eights weeks, along with self-practice.

Eligibility

Sex/Gender
ALL
Age
65 Years to 95 Years
Healthy volunteers
Yes

Inclusion criteria

1. age 65 years or above, 2. able to walk for 10 feet without human assistance, a cane or walker was permitted, 3. willing to wear an ActiGraph activity monitor for 7 days at baseline and post-intervention test, 4. exercise safely as determined by their healthcare provider, 5. complete the study tests and questionnaires, 6. sign the informed consent, 7. able and willing to comply with the requirements of the protocol.

Exclusion criteria

1. having recent medical limitations including recent myocardial infarction, stroke, or physical limitations for exercises by completing the Physical Activity Readiness Questionnaire (PAR-Q), 2. having 40 or higher body mass index (BMI) by self-reporting body weight and body height, inputting these into the computerized BMI calculator.

Design outcomes

Primary

MeasureTime frameDescription
Weekly Physical Activity MinutesBaseline test and post-intervention test (up to 3 months).Weekly physical activity minutes were measured by having participants wear an ActiGraph activity monitor for seven consecutive days during waking hours, expect for bathing activities. The raw data were analyzed by using the ActiLife software.
Short Physical Performance Battery (SPPB)-Repeated Chair Stand test.Baseline test and post-intervention test (up to 3 months).This test is used to measure low extremity strength.
The Short Physical Performance Battery-Balance test.Baseline and post-intervention test (Up to 3 months).This test is used to measure balance.

Secondary

MeasureTime frameDescription
Timed Up and Go TestBaseline test and the post-intervention test (up to 3 months).This test is used to measure gait speed.
The Patient-Reported Outcomes Measurement Information System (PROMIS) Physical Function Short FormBaseline test and post-intervention test (up to 3 months).This questionnaire is used to assess participants' perceived physical function.
Assessing Feasibility, Acceptability, and Appropriateness of the Intervention QuestionnairePost-intervention test (up to one week).This questionnaire is used to assess the participant's views of feasibility, acceptability, and appropriateness of the intervention.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026