- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04901910
Social Media Intervention - Physical Activity
Social Media Intervention for Cannabis Use and Physical Activity in Emerging Adults - Physical Activity
The purpose of the study is to develop and test social media interventions to help young people increase well-being and reduce risky behaviors. The study will help us learn about ways to deliver wellness information in a way that is appealing and helpful to young people that use social media.
Eligible participants will be enrolled after baseline survey is completed. Participants will be involved with the secret social media group they are assigned to for 8 weeks. In addition, surveys will be completed at various times during and after the 8 week social media group.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Michigan
-
Ann Arbor, Michigan, United States, 48109
- University of Michigan
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- self-report using cannabis at least 3 times per week or more often in the past month
- active Facebook profile
Exclusion Criteria:
- participants who cannot read English will be informally excluded
if participants fail identity verification based on:
- Internet Protocol (IP) addresses
- survey time completion
- repeat attempts
- survey responses
- photo identification from a time stamped self picture sent to the research team
- cannot safely engage in moderate to vigorous physical activity [assessed at screening]
- participated in previous Project Verdi waves
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Physical Activity (PA) Social Media Group
This will be an 8 week Social Media Group available to the participant focused on health and well-being.
|
Participants will have access to the secret Social Media page that will deliver health information focused on increasing healthy activities and well-being.
This information will be posted by e-coaches.
Participants can interact with the e-coaches as well as other study members in the group.
|
Experimental: Verdi plus PA Social Media Group
This will be an 8 week Social Media Group available to the participant focused on health and well-being.
|
Participants will have access to the secret Social Media page that will deliver health information focused on increasing healthy activities, well-being, and reducing risky behaviors.
This information will be posted by e-coaches.
Participants can interact with the e-coaches as well as other study members in the group.
|
No Intervention: Attention-Control condition Social Media Group
This will be an 8 week Social Media Group available to the participant with social media topics.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Acceptability of intervention (i.e., ratings of e-coaches, )
Time Frame: 3 months (after baseline)
|
Acceptability ratings completed by participants: How helpful were the e-coaches?
|
3 months (after baseline)
|
Acceptability of intervention (i.e., helpfulness of peer interaction)
Time Frame: 3 months (after baseline)
|
Acceptability ratings completed by participants: How helpful was it to interact with other peers in the group?
|
3 months (after baseline)
|
Feasibility of intervention as evidenced by metrics of key activities (accepting group invitation)
Time Frame: 8 weeks post-group start
|
number/percent who accept group invite
|
8 weeks post-group start
|
Feasibility of intervention as evidenced by metrics of key activities (engaging in the group)
Time Frame: 8 weeks post-group start
|
number/percent who comment engage (i.e., comment at least one time)
|
8 weeks post-group start
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Erina Bonar, PhD, University of Michigan
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- HUM00195927
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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