- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06570083
Mobile-Based Intervention to Promote Physical Activity Among the Elderly
Mobile-Based Intervention to Promote Physical Activity Among the Elderly With Chronic Diseases
Study Overview
Status
Conditions
Intervention / Treatment
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
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Xue Weng
- Phone Number: 3621259
- Email: xueweng@bnu.edu.cn
Study Locations
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Guangdong
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Zhuhai, Guangdong, China, 519087
- Beijing Normal University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Age ≥60 years and diagnosed with at least one chronic disease
- Owns a smartphone and is proficient in using WeChat
- Daily sedentary time ≥6 hours
Exclusion Criteria:
- recent surgeries, injuries, or other conditions that would prevent simple physical activity
- hearing, vision, or physical disabilities
Study Plan
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 |
|---|---|
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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.
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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.
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|
Active Comparator: Control group
Participants in the control group will receive a self-help booklet designed to promote physical activity among the elderly.
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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.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Time spent in sedentary behavior
Time Frame: 3 and 6 months follow-up
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The time spent sedentary behavior (min/week) in the last 7 days
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3 and 6 months follow-up
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Acceptability of the Mobile Phone-Based Intervention
Time Frame: 3 and 6 months follow-up
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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.
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3 and 6 months follow-up
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Perceived Usefulness of the Mobile Phone-Based Intervention
Time Frame: 3 and 6 months follow-up
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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.
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3 and 6 months follow-up
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Time spent in zero-time exercise
Time Frame: 3 and 6 months follow-up
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The time spent physical activity while seated and standing (min/week) in the last 7 days
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3 and 6 months follow-up
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Exercise self-efficacy
Time Frame: 3 and 6 months follow-up
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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.
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3 and 6 months follow-up
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Anxiety and depression
Time Frame: 3 and 6 months follow-up
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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.
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3 and 6 months follow-up
|
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Perceived subjective happiness
Time Frame: 3 and 6 months follow-up
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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.
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3 and 6 months follow-up
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Perceived life satisfaction
Time Frame: 3 and 6 months follow-up
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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.
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3 and 6 months follow-up
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
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)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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