Change in Social Media Use and Well-being Among College Students Receiving a One-week Exercise or Mindfulness Intervention

Comparing Change in Social Media Use and Well-being Among College Students Receiving a One-week Exercise or Mindfulness Intervention

The investigators will be randomizing 150 college student participants with high levels of social media use into either a 1) control condition (no intervention), a 2) mindfulness meditation cognitive intervention, or 3) a social media reduction + exercise replacement intervention. Participants complete intervention activities daily for one week. The investigators will collect self-report and behavioral measures of social media use and related psychological constructs at three time points: baseline, immediately after the intervention period, and one-week after the intervention period.

Study Overview

Detailed Description

The objective of this study is to test two cognitive and behavioral interventions designed to reduce social media use and psychological constructs related to social media use in a sample of university students.

The first cognitive intervention is a mindfulness meditation exercise taken from the Calm app centering around gratitude. Each meditation takes approximately 12 minutes to complete and is to be done daily for one week. The second behavioral intervention is asking participants to reduce social media use for 30 minutes daily for one week and replacing that time with physical exercise of the participants' choosing.

Aim 1: Compare psychological constructs related to mental health (well-being, stress, depression, anxiety, loneliness, social comparisons, etc.) before and after conducting two social media use interventions over a period of one week, compared to a control condition (no intervention).

Aim 2: Compare self-reported and behavioral (smartphone screen shots of social media use screen time) measures of social media use before and after two social media use interventions over a period of over one week, compared to a control condition (no intervention).

Aim 3: Examine mental health and social media use one week after the intervention period is complete (follow up), examining or testing whether effects last beyond the intervention period.

Study Type

Interventional

Enrollment (Estimated)

150

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

  • Name: Timothy L Regan, PhD
  • Phone Number: 240-643-9090
  • Email: tregan2@jh.edu

Study Contact Backup

  • Name: Johannes Thrul, PhD
  • Phone Number: 510-646-7860
  • Email: jthrul@jhu.edu

Study Locations

    • Maryland
      • Baltimore, Maryland, United States, 21218
        • Recruiting
        • Johns Hopkins University
        • Contact:
          • Johannes Thrul

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

Yes

Description

Inclusion Criteria:

  • The participant is 18 or older.
  • The participant must be a Johns Hopkins University student.
  • Owning an iPhone or Android smartphone, with frequent use of social media use daily (> 1 hour)
  • Enabling and sharing screenshots of your smartphone use metrics, including number of last-week pickups, notifications received, and average screen time.
  • Providing consent to participate.
  • Only exercising 1 hour or less daily, on average.

Exclusion Criteria:

  • younger than 18
  • Not a Johns Hopkins University Student
  • Doesn't own a smart phone
  • Uses smartphone less than 1 hour daily
  • Exercises more than 1 hour daily

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: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Control
Participants will not receive an intervention. They will receive instructions to use their social media use as usual.
Experimental: Mindfulness
Approximately 12-minute mindfulness-style meditations will be completed daily for one week through the Calm platform. Participants can listen to the exercise on the web-enabled version of Calm, or through the smartphone app. The course is entitled "7 Days of Gratitude" and centers around noticing and appreciating things in daily life.
12 minute daily guided meditation
Experimental: Social Media Reduction + Exercise
Participants will reduce their social media use by at least 30 minutes daily for one week. Simultaneously, participants will exercise at least 30 minutes daily. Participants are given examples of common exercises (walking, yoga, strength training, etc.), but they are allowed to choose any type, although they are dissuaded from activities with high potential for injury.
Reduce social media use at least 30 minutes daily and exercise instead

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Depression, Anxiety and Stress Scale - 21 (DASS-21)
Time Frame: baseline, immediately post intervention, post intervention up to one week
Score range = 0-63, higher score = worse outcome
baseline, immediately post intervention, post intervention up to one week
Change in World Health Organization Quality of Life (WHOQoL-BREF) scale
Time Frame: baseline, immediately post intervention, post intervention up to one week
Score range = 13-65, lower score = worse outcome
baseline, immediately post intervention, post intervention up to one week
Change in Smartphone screen time (minutes) for social media use
Time Frame: baseline, immediately post intervention, post intervention up to one week
Past-week amount of screen time for social media use
baseline, immediately post intervention, post intervention up to one week
Change in Number of Social media use smartphone pick-ups
Time Frame: baseline, immediately post intervention, post intervention up to one week
Past-week total number of smartphone pick-ups for social media use applications
baseline, immediately post intervention, post intervention up to one week
Change in Percent of time using social media
Time Frame: baseline, immediately post intervention, post intervention up to one week
Past-week percent of time using social media compared to other smartphone application categories.
baseline, immediately post intervention, post intervention up to one week
Change in Social media use notifications received
Time Frame: baseline, immediately post intervention, post intervention up to one week
Past-week total number of notifications received for social media use applications
baseline, immediately post intervention, post intervention up to one week

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in University of California, Los Angeles 3-Item Loneliness Scale
Time Frame: baseline, immediately post intervention, post intervention up to one week
Score range = 3-9, higher score = worse outcome
baseline, immediately post intervention, post intervention up to one week
Change in The Gratitude Questionnaire, 6-item form (GQ-6) scale
Time Frame: baseline, immediately post intervention, post intervention up to one week
Score range = 6-42, lower score = worse outcome
baseline, immediately post intervention, post intervention up to one week
Change in Motivations for Electronic Interaction Scale (MEIS)
Time Frame: baseline, immediately post intervention, post intervention up to one week
Score range = 10-50, higher score = worse outcome
baseline, immediately post intervention, post intervention up to one week
Change in Comprehensive Assessment of Acceptance and Commitment Therapy Processes (CompACT-15) scale
Time Frame: baseline, immediately post intervention, post intervention up to one week
Score range = 0-138, lower scores = worse outcome
baseline, immediately post intervention, post intervention up to one week
Change in Bergen Social Media Addiction Scale (BSMAS)
Time Frame: baseline, immediately post intervention, post intervention up to one week
Score range = 6-35, higher score = worse outcome
baseline, immediately post intervention, post intervention up to one week
Change in Fear of Missing Out Scale
Time Frame: baseline, immediately post intervention, post intervention up to one week
Score range = 10-50, higher score = worse outcome
baseline, immediately post intervention, post intervention up to one week
Change in Hours spent socializing in-person with peers
Time Frame: baseline, immediately post intervention, post intervention up to one week
Score range = 0-20+ hours of in-person socialization, lower scores = worse outcomes
baseline, immediately post intervention, post intervention up to one week
Change in Number of evenings of past-week recreation
Time Frame: baseline, immediately post intervention, post intervention up to one week
Score range = 0-7 evenings of recreation, lower scores = worse outcomes
baseline, immediately post intervention, post intervention up to one week

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Johannes Thrul, Johns Hopkins Bloomberg School of Public Health

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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)

February 7, 2024

Primary Completion (Estimated)

May 31, 2024

Study Completion (Estimated)

May 31, 2024

Study Registration Dates

First Submitted

November 14, 2023

First Submitted That Met QC Criteria

November 16, 2023

First Posted (Actual)

November 22, 2023

Study Record Updates

Last Update Posted (Actual)

February 12, 2024

Last Update Submitted That Met QC Criteria

February 9, 2024

Last Verified

February 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • IRB00025926

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

We will discuss as a team the how to share individual participant data with other researchers in a confidential manner.

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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