Social Media Intervention - Physical Activity

March 25, 2022 updated by: Erin Bonar, University of Michigan

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

Study Type

Interventional

Enrollment (Actual)

60

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

    • Michigan
      • Ann Arbor, Michigan, United States, 48109
        • University of Michigan

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

18 years to 25 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

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

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: 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?

  1. Not at all
  2. A little
  3. Somewhat
  4. Very Much
  5. Extremely
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?

  1. Not at all
  2. A little
  3. Somewhat
  4. Very Much
  5. Extremely
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

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

Investigators

  • Principal Investigator: Erina Bonar, PhD, University of Michigan

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)

May 18, 2021

Primary Completion (Actual)

December 25, 2021

Study Completion (Actual)

December 25, 2021

Study Registration Dates

First Submitted

May 14, 2021

First Submitted That Met QC Criteria

May 20, 2021

First Posted (Actual)

May 26, 2021

Study Record Updates

Last Update Posted (Actual)

March 28, 2022

Last Update Submitted That Met QC Criteria

March 25, 2022

Last Verified

March 1, 2022

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • HUM00195927

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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