Mobile-Based Intervention to Promote Physical Activity Among the Elderly

August 22, 2024 updated by: Beijing Normal University

Mobile-Based Intervention to Promote Physical Activity Among the Elderly With Chronic Diseases

This study aims to explore the feasibility and preliminary effectiveness of a mobile phone-based intervention among elderly individuals with chronic diseases.

Study Overview

Detailed Description

Promoting physical activity among elderly individuals is an increasingly critical public health priority. Regular exercise is essential for maintaining mobility, enhancing mental well-being, and reducing the risk of exacerbating chronic conditions. However, many elderly individuals encounter significant barriers, including physical limitations, lack of motivation, and restricted access to safe environments.

This mobile phone-based intervention seeks to address these challenges by offering accessible support through age-appropriate exercise routines, motivational prompts, and educational content delivered directly to participants' mobile devices. The intervention's primary objective is to reduce sedentary behavior, increase physical activity levels, and ultimately enhance the overall health and well-being of elderly individuals with chronic diseases.

Study Type

Interventional

Enrollment (Estimated)

200

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 Contact

Study Locations

    • Guangdong
      • Zhuhai, Guangdong, China, 519087
        • Beijing Normal 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

No

Description

Inclusion Criteria:

  1. Age ≥60 years and diagnosed with at least one chronic disease
  2. Owns a smartphone and is proficient in using WeChat
  3. Daily sedentary time ≥6 hours

Exclusion Criteria:

  1. recent surgeries, injuries, or other conditions that would prevent simple physical activity
  2. hearing, vision, or physical disabilities

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: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Intervention group
Participants in the intervention group will receive three months of personalized support via WeChat, including tailored exercise recommendations, motivational messages, and educational content.
Participants receive three months of personalized support via WeChat, including tailored exercise recommendations, motivational messages, and educational content.
Participants receive a self-help booklet to promote physical activity among the elderly. The booklet will include guidelines for safe and effective exercises, tips for staying motivated, and information on the health benefits of regular physical activity.
Active Comparator: Control group
Participants in the control group will receive a self-help booklet designed to promote physical activity among the elderly.
Participants receive a self-help booklet to promote physical activity among the elderly. The booklet will include guidelines for safe and effective exercises, tips for staying motivated, and information on the health benefits of regular physical activity.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Time spent in sedentary behavior
Time Frame: 3 and 6 months follow-up
The time spent sedentary behavior (min/week) in the last 7 days
3 and 6 months follow-up
Acceptability of the Mobile Phone-Based Intervention
Time Frame: 3 and 6 months follow-up
Acceptability will be assessed using a series of 4 items from previous studies on mobile physical activity interventions. Participants will rate each statement on a 5-point Likert scale, ranging from 1 (strongly disagree) to 5 (strongly agree). The statements will cover aspects such as ease of use, personal relevance, clarity of information, and overall satisfaction with the intervention.
3 and 6 months follow-up
Perceived Usefulness of the Mobile Phone-Based Intervention
Time Frame: 3 and 6 months follow-up
Perceived usefulness will be assessed using 5 items from previous studies on online physical activity interventions. Participants will rate each question on a 5-point Likert scale, ranging from 1 (not at all useful) to 5 (very useful). The questions will explore how useful participants found the intervention in helping them to (1) increase confidence in engaging in regular physical activity, (2) overcome barriers to physical activity, (3) increase support for participating in physical activity, (4) plan for physical activity, and (5) stay motivated to engage in physical activity.
3 and 6 months follow-up

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Time spent in zero-time exercise
Time Frame: 3 and 6 months follow-up
The time spent physical activity while seated and standing (min/week) in the last 7 days
3 and 6 months follow-up
Exercise self-efficacy
Time Frame: 3 and 6 months follow-up
This outcome measure evaluates participants' confidence in their ability to engage in regular physical activity (self-efficacy). Participants will rate their confidence on a single-item scale ranging from 1 to 10, with higher scores indicating greater self-efficacy.
3 and 6 months follow-up
Anxiety and depression
Time Frame: 3 and 6 months follow-up
Anxiety and depression levels will be assessed using the Patient Health Questionnaire-4 (PHQ-4), a validated tool comprising two items for anxiety and two items for depression. The PHQ-4 score ranges from 0 to 12, with higher scores indicating greater severity of anxiety and depression symptoms.
3 and 6 months follow-up
Perceived subjective happiness
Time Frame: 3 and 6 months follow-up
This outcome measure assesses participants' subjective happiness using a Self-Reported Happiness scale. Participants will rate their happiness on a single-item scale ranging from 1 (not at all happy) to 5 (extremely happy), with higher scores indicating greater perceived happiness.
3 and 6 months follow-up
Perceived life satisfaction
Time Frame: 3 and 6 months follow-up
This outcome measure assesses participants' subjective life satisfaction using a self-reported life satisfaction scale. Participants will rate their life satisfaction on a single-item scale ranging from 1 to 5, with higher scores indicating greater perceived life satisfaction.
3 and 6 months follow-up

Collaborators and Investigators

This is where you will find people and organizations involved with this 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 (Estimated)

September 1, 2024

Primary Completion (Estimated)

September 30, 2025

Study Completion (Estimated)

September 30, 2026

Study Registration Dates

First Submitted

August 20, 2024

First Submitted That Met QC Criteria

August 22, 2024

First Posted (Actual)

August 26, 2024

Study Record Updates

Last Update Posted (Actual)

August 26, 2024

Last Update Submitted That Met QC Criteria

August 22, 2024

Last Verified

August 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • Mobile Elderly Exercise

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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