- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03803085
A Group-Based Walking Study Using WeChat to Enhance Physical Activity Among Older Adults
A Group-Based Walking Study Using WeChat to Enhance Physical Activity Among Older Adults: The Role of Social Engagement
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The aim for the study is to use the function WeRun in the application WeChat to encourage physical activity and social engagement among community dwelling older adults. The investigators asked participants in the social engagement group to use the WeRun function in WeChat to track their daily walking steps and to compare their performance with their group members for 4 weeks. To encourage social engagement among their group members, the daily walking steps were calculated and the participant who has the highest step count in the group will be indicated each day.Those in the control group will only use the WeRun function in WeChat to track their own walking steps.
The investigators expected that the participants in the social contact group will walk more often and report more social activities than those in the control group, who will not compete with their peers in daily walking. To test these predictions, daily walking steps and the total walking steps per week were obtained and compared across groups. The nature and the extent of change was analyzed over the four weeks. Exercise self-efficacy was measured using a measure based on Bandura's model. Social engagement was measured using the short Lubben Social Network Scale, a self report measure of social engagement on a 12-item scale, and physical activity was measured using International Physical Activity Questionnaire (IPAQ), a self-report measure of physical activity on a 12-item scale.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Massachusetts
-
Waltham, Massachusetts, United States, 02453
- Brandeis University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Participants who are 60 or older who have a cellphone, with either android or iPhone system with data plan.
- They must be fit enough to walk for at least 20 minutes at a time.
- English speaking
Exclusion Criteria:
- Unable to walk more than 20 minutes;
- do not have smart phone with data plan.
- younger than 60
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Control Condition
Participants only saw their own daily walking steps using the WeRun function in WeChat.
They did not use WeChat to see other group members' daily steps and did not engage in social contact with their group members.
|
Participants in the control group only saw their own daily walking steps using the WeChat.
They did not use WeChat to see other group members' daily steps and did not contact other group members.
The participants were asked to use the app every day.
A message (through WeChat) was sent to remind them to use the application if they had not done so within three days.
|
|
Experimental: Treatment condition
Participants saw their own and other group member's daily walking steps using the WeRun function in WeChat and they were able to contact the other members of their group using We Chat.
|
Participants in the experimental condition used WeChat for 4 weeks to see their own and other's walking steps and also were able to contact other group members.
The participants were asked to use the application every day.
A message (through the group chat) was sent to remind them to use the application if they have not done so within three days.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Number of Steps Walked
Time Frame: [Time Frame: Baseline (pretest) Week, Week 4 (posttest) and Week 8 (one month follow up)]
|
Weekly average number of steps recorded with WeRun on the phone [ (averaged across 7 days at Baseline week and averaged across 7 days at Week 4 (Posttest) and averaged across 7 days at Week 8 (one month follow up)].
|
[Time Frame: Baseline (pretest) Week, Week 4 (posttest) and Week 8 (one month follow up)]
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Social Engagement
Time Frame: Pretest given 1 week before the intervention and then at the posttest after the 4 week study and one month follow up
|
Short Lubben Social Network Scale-Revised, a self-report measure of social engagement on a 12-item scale.
The total score is calculated by the sum of all the items.
The total score ranges between 0 and 60, with a higher score indicating more social engagement.
|
Pretest given 1 week before the intervention and then at the posttest after the 4 week study and one month follow up
|
|
Exercise Self Efficacy
Time Frame: Pretest given 1 week before the intervention and then at the posttest after the 4 week study and one month follow up
|
This scale is a self-report of exercise self-efficacy.
Total score is calculated by summing the responses to each question.
This scale has a range of total scores from 0-90.
A higher score indicates higher self-efficacy for exercise.
|
Pretest given 1 week before the intervention and then at the posttest after the 4 week study and one month follow up
|
Collaborators and Investigators
Sponsor
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
- 18131
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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