A Novel Mat Exercise Program Improves Functional Fitness, Activity Levels, and Quality of Life in Older Adults

March 26, 2025 updated by: Wen Ching Huang, National Taipei University of Nursing and Health Sciences

The Title Used in the Study Protocol: Professor

In this study, investigators recruited older adults aged 60 to 80 years and utilized a parallel experimental design. A total of 32 participants were randomly assigned to either the experimental or control group. The intervention consisted of a 70-min-long exercise game-based mat training session conducted twice weekly for 10 consecutive weeks. Each session included a 10-min warm-up, approximately 45 min of primary training, and a 15-min cool-down and stretching routine. Participants completed the International Physical Activity Questionnaire (IPAQ) and the World Health Organization Quality of Life questionnaire (WHOQOL, Taiwanese Version) before and after the intervention. Additionally, the functional fitness assessment were conducted.

Study Overview

Detailed Description

The mat-based exercise facility (Stampede, Taipei, Taiwan) assists participants in exercise training by incorporating interactive light and sound effects to guide users through various exercises while progressively increasing intensity. The training program is divided into two phases: the first phase focuses on fundamental movements, whereas the second phase introduces more advanced exercises. With progress, additional exercise equipment is incorporated, along with increased sets, duration, movement variations, and training intensity. Training sessions can be conducted in a simple, progressive manner or a game-competitive format. Throughout the training, participants wore a heart rate monitor (ALATHEC Obeat1, Taichung, Taiwan) that recorded their exercise intensity and heart rate fluctuations. However, the exercise intensity and frequency were adjusted based on participants' adaptation. This study encompassed five different lighting modes, namely all light on, circle on, four corners, two lines, and diamond. Each mode was paired with different training protocols and movement patterns, supplemented by training equipment, such as medicine balls, resistance bands, and balance pads.

Study Type

Interventional

Enrollment (Actual)

32

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

      • Taipei, Taiwan, 112303
        • National Taipei University of Nursing and Health Sciences

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:

(i) Elderly individuals (aged 60-80) who have not experienced any muscle or skeletal injuries in the past month and are able to participate in training normally.

(ii) Completion of the Physical Activity Readiness Questionnaire and meeting the conditions for initiating moderate-intensity exercise intervention.

(iii) Ability to comply with the exercise frequency required by this study and travel to and from the training site independently.

Exclusion Criteria:

(i) individuals with severe musculoskeletal disorders, (ii) individuals deemed unsuitable for exercise training based on a Physical Activity Readiness Questionnaire evaluation or psychiatric disorders, and (iii) individuals under medications that may influence study outcomes.

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: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: The implementation of novel exercise mat training program
The mat-based exercise facility (Stampede, Taipei, Taiwan) assists participants in exercise training by incorporating interactive light and sound effects to guide users through various exercises while progressively increasing intensity.Participants were randomly assigned to either the experimental or control group. The experimental group underwent a 10-week-long exercise game-based mat training, consisting of two sessions per week (70 min/session), using group-based exercise training.
The training program is divided into two phases: the first phase focuses on fundamental movements, whereas the second phase introduces more advanced exercises. With progress, additional exercise equipment is incorporated, along with increased sets, duration, movement variations, and training intensity. Training sessions (10-week duration) can be conducted in a simple, progressive manner or a game-competitive format.The control group maintained their usual daily activities.
Active Comparator: Active control
The control group maintained their usual daily activities as active comparator.
The control group maintained their usual daily activities.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
International Physical Activity Questionnaire
Time Frame: The evaluation was conducted at baseline and the 11th week time points.
The questionnaire was applied to evaluate the physical activities. The duration of activity will be converted into metabolic equivalents (METs), with higher MET values indicating a greater level of physical activity.
The evaluation was conducted at baseline and the 11th week time points.
World Health Organization Quality of Life questionnaire
Time Frame: The evaluation was conducted at baseline and the 11th week time points.
The questionnaire was applied to evaluate the quality of life. A self-assessment will be conducted for different dimensions of quality of life, with higher values indicating greater satisfaction in that particular dimension.
The evaluation was conducted at baseline and the 11th week time points.
Senior fitness
Time Frame: The evaluation was conducted at baseline and the 11th week time points.
The regular physical fitness was evaluated by indicated senior fitness test. This fitness test measures the number of repetitions performed within a specific time frame, with higher values indicating better fitness. However, for dynamic balance, a shorter time indicates better performance.
The evaluation was conducted at baseline and the 11th week time points.
Functional fitness
Time Frame: The evaluation was conducted at baseline and 11th week time points.
The functional fitness was evaluated by sport technology-based AFAscan fitness assessment. This fitness test measures the number of repetitions performed within a specific time frame, with higher values indicating better fitness.
The evaluation was conducted at baseline and 11th week time points.

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Wen-Ching Huang, Ph.D., National Taipei University of Nursing and Health Sciences

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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)

August 1, 2024

Primary Completion (Actual)

February 28, 2025

Study Completion (Estimated)

June 30, 2025

Study Registration Dates

First Submitted

March 12, 2025

First Submitted That Met QC Criteria

March 20, 2025

First Posted (Actual)

March 27, 2025

Study Record Updates

Last Update Posted (Actual)

April 1, 2025

Last Update Submitted That Met QC Criteria

March 26, 2025

Last Verified

March 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • C112161
  • NSTC (Other Identifier: National Science and Technology Council)

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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