Physical Activity Promoting Active Aging

June 25, 2026 updated by: Yu Wang

Physical Activity Promoting Active Aging: An Exploration of Intrinsic Mechanisms and Practical Pathways

This project aims to explore the effects and underlying mechanisms of physical activity in promoting active aging among older adults. The researchers conducted two rounds of progressive randomized controlled intervention trials to verify the effects and mechanisms of a multimodal physical activity intervention on active aging from two dimensions: intervention structure and participation mode.

In Study 1, with a 12-week intervention period, participants were randomly assigned to three groups: a Tai Chi exercise group, a multimodal exercise group, and a daily activity control group. By comparing between-group differences, the study evaluated the effects of different exercise modalities on physical function and subjective active aging.

In Study 2, also with a 12-week intervention period, participants were randomly assigned to two multimodal exercise groups differing in participation mode: an in-person group-based format versus an online individual format. This study examined the moderating effects of different participation modes on both objective and subjective active aging outcomes, while keeping the multimodal physical activity intervention content identical.

Study Overview

Study Type

Interventional

Enrollment (Actual)

100

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Zhejiang
      • Hangzhou, Zhejiang, China, 310058
        • Department of Sports Science, College of Education, Zhejiang University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Aged 60 years or above;

Capable of engaging in regular physical activities and comprehending basic testing procedures and instructions.

Exclusion Criteria:

  • Severe cardiac, pulmonary, or musculoskeletal disorders;

History of neurological or psychiatric conditions that may impair cognitive function (e.g., stroke, Parkinson's disease, Alzheimer's disease, major depressive disorder, etc.);

Missing three or more scheduled intervention sessions during the study period, or requesting discontinuation of participation.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Control group
Experimental: Multicomponent exercise group
Tai Chi, Baduanjin, strength, balance, and flexibility exercises
Experimental: Mind-body exercise group
Tai Chi, Yoga, and Baduanjin
Experimental: Online-based multicomponent exercise group
Tai Chi, Baduanjin, and strength, balance, and flexibility exercises (delivered via live online streaming and video watching)
Experimental: In-person multicomponent exercise group
Tai Chi, Baduanjin, and strength, balance, and flexibility exercises (delivered in an in-person group format)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Active aging
Time Frame: week0, week6, week12
It was measured using the Active Aging Questionnaire.
week0, week6, week12
General self-efficacy
Time Frame: week0, week6, week12
It was measured using the General Self-Efficacy Scale.
week0, week6, week12
Cognitive function
Time Frame: week0, week6, week12
Cognitive function was measured using the cognitive subscale of the LEIPAD questionnaire
week0, week6, week12
Cognitive function assessed by the Montreal Cognitive Assessment (MOCA)
Time Frame: week0, week6, week12
Cognitive function was measured using the Montreal Cognitive Assessment (MOCA).
week0, week6, week12

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Height
Time Frame: week0, week6, week12
week0, week6, week12
Weight
Time Frame: week0, week6, week12
week0, week6, week12
Body fat percentage
Time Frame: week0, week6, week12
week0, week6, week12
Vital capacity test
Time Frame: week0, week6, week12
Physiological parameter
week0, week6, week12
2-minute high-knee marching in place
Time Frame: week0, week6, week12
week0, week6, week12
Handgrip strength
Time Frame: week0, week6, week12
week0, week6, week12
Sit and reach test
Time Frame: week0, week6, week12
week0, week6, week12
30-second chair stand test
Time Frame: week0, week6, week12
Physiological parameter
week0, week6, week12
One-legged stance with eyes closed tesr
Time Frame: week0, week6, week12
Physiological parameter
week0, week6, week12
Choice reaction time
Time Frame: week0, week6, week12
week0, week6, week12

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 1, 2026

Primary Completion (Actual)

June 20, 2026

Study Completion (Actual)

June 20, 2026

Study Registration Dates

First Submitted

June 20, 2026

First Submitted That Met QC Criteria

June 25, 2026

First Posted (Actual)

June 26, 2026

Study Record Updates

Last Update Posted (Actual)

June 26, 2026

Last Update Submitted That Met QC Criteria

June 25, 2026

Last Verified

June 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • ZJU-SSEC/2025/No.6
  • 23NDJC001Z (Other Grant/Funding Number: Key Program of Philosophy and Social Sciences Planning of Zhejiang Province)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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