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

Sponsor
Johns Hopkins Bloomberg School of Public Health (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06143852
Collaborator
(none)
150
3
4

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Mindfulness
  • Behavioral: Social Media Reduction + Exercise
N/A

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 Design

Study Type:
Interventional
Anticipated Enrollment :
150 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Three groups of 1) no intervention, 2) mindfulness, or 3) social media reduction + exercise replacement intervention armsThree groups of 1) no intervention, 2) mindfulness, or 3) social media reduction + exercise replacement intervention arms
Masking:
None (Open Label)
Masking Description:
Both participants and investigators will know which intervention group each participant has been randomized into.
Primary Purpose:
Treatment
Official Title:
Comparing Change in Social Media Use and Well-being Among College Students Receiving a One-week Exercise or Mindfulness Intervention
Anticipated Study Start Date :
Jan 1, 2024
Anticipated Primary Completion Date :
May 1, 2024
Anticipated Study Completion Date :
May 1, 2024

Arms and Interventions

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.

Behavioral: Mindfulness
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.

Behavioral: Social Media Reduction + Exercise
Reduce social media use at least 30 minutes daily and exercise instead

Outcome Measures

Primary Outcome Measures

  1. Change in Depression, Anxiety and Stress Scale - 21 (DASS-21) [baseline, immediately post intervention, post intervention up to one week]

    Score range = 0-63, higher score = worse outcome

  2. Change in World Health Organization Quality of Life (WHOQoL-BREF) scale [baseline, immediately post intervention, post intervention up to one week]

    Score range = 13-65, lower score = worse outcome

  3. Change in Smartphone screen time (minutes) for social media use [baseline, immediately post intervention, post intervention up to one week]

    Past-week amount of screen time for social media use

  4. Change in Number of Social media use smartphone pick-ups [baseline, immediately post intervention, post intervention up to one week]

    Past-week total number of smartphone pick-ups for social media use applications

  5. Change in Percent of time using social media [baseline, immediately post intervention, post intervention up to one week]

    Past-week percent of time using social media compared to other smartphone application categories.

  6. Change in Social media use notifications received [baseline, immediately post intervention, post intervention up to one week]

    Past-week total number of notifications received for social media use applications

Secondary Outcome Measures

  1. Change in University of California, Los Angeles 3-Item Loneliness Scale [baseline, immediately post intervention, post intervention up to one week]

    Score range = 3-9, higher score = worse outcome

  2. Change in The Gratitude Questionnaire, 6-item form (GQ-6) scale [baseline, immediately post intervention, post intervention up to one week]

    Score range = 6-42, lower score = worse outcome

  3. Change in Motivations for Electronic Interaction Scale (MEIS) [baseline, immediately post intervention, post intervention up to one week]

    Score range = 10-50, higher score = worse outcome

  4. Change in Comprehensive Assessment of Acceptance and Commitment Therapy Processes (CompACT-15) scale [baseline, immediately post intervention, post intervention up to one week]

    Score range = 0-138, lower scores = worse outcome

  5. Change in Bergen Social Media Addiction Scale (BSMAS) [baseline, immediately post intervention, post intervention up to one week]

    Score range = 6-35, higher score = worse outcome

  6. Change in Fear of Missing Out Scale [baseline, immediately post intervention, post intervention up to one week]

    Score range = 10-50, higher score = worse outcome

  7. Change in Hours spent socializing in-person with peers [baseline, immediately post intervention, post intervention up to one week]

    Score range = 0-20+ hours of in-person socialization, lower scores = worse outcomes

  8. Change in Number of evenings of past-week recreation [baseline, immediately post intervention, post intervention up to one week]

    Score range = 0-7 evenings of recreation, lower scores = worse outcomes

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Johns Hopkins Bloomberg School of Public Health

Investigators

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

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Johns Hopkins Bloomberg School of Public Health
ClinicalTrials.gov Identifier:
NCT06143852
Other Study ID Numbers:
  • IRB00025926
First Posted:
Nov 22, 2023
Last Update Posted:
Nov 22, 2023
Last Verified:
Nov 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 22, 2023