CClinicalTrials.gg
RecruitingNCT07097545SMUSUpdated Dec 17, 2025

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

An interventional study of Mindfulness and Social Media Reduction in Social Media Addiction, Anxiety and Depression Disorder, sponsored by Johns Hopkins Bloomberg School of Public Health. Recruiting at 1 site in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-12-17.

Sponsored by Johns Hopkins Bloomberg School of Public Health · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Started Aug 2025; still recruiting 1 year 1 month later.
Phase
Not applicable
Study type
Interventional
Enrollment
300
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The investigators will be randomizing 300 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 two weeks. 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 (three weeks from baseline).

Read the detailed description

The objective of this study is to test two cognitive and behavioral interventions designed to reduce social media use and improve psychological constructs related to social media use in a sample of university students. The cognitive intervention is a mindfulness meditation exercise taken from the Calm app focused around gratitude and stress management. Each meditation takes approximately 15 minutes to complete and is to be done daily for two week. The second behavioral intervention is asking participants to reduce social media use for 30 minutes daily for two weeks 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 two weeks, compared to a control condition (no intervention).

Aim 2: Compare self-reported and behavioral (smartphone screenshots of social media use screentime) measures of social media use before and after two social media use interventions over two weeks, compared to a control condition (no intervention).

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

02

Conditions studied

  • Social Media Addiction
  • Anxiety
  • Depression Disorder
  • Wellbeing

Keywords

  • digital media reduction intervention
  • mindfulness
  • behavioral intervention
  • digital wellbeing
03

In context

Internet Addiction Disorder

170 studies on the registry are indexed under Internet Addiction Disorder; 49 are open to participants now.

This study's planned enrollment of 300 is above the median of 88 across 95 interventional studies indexed under Internet Addiction Disorder.

Browse Internet Addiction Disorder studies →

Lead sponsor

Johns Hopkins Bloomberg School of Public Health is the lead sponsor of 364 studies on the registry; 41 are open to participants now.

Of its 5 completed or terminated interventional studies of FDA-regulated products, 3 (60%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
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 the participant's 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

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
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
300 participants (estimated)

Study arms

  • No intervention
    Control

    Participants will not receive an intervention. Participants will receive instructions to use social media use as usual.

  • Experimental
    Mindfulness

    Approximately 15 minute mindfulness style meditations will be completed daily for two weeks through the Calm platform. Participants can listen to the exercise on the web-enabled version of Calm, or through the smartphone app. The first course is entitled "7 Days of Gratitude" and centers around noticing and appreciating things in daily life, the second course is entitled "7 Days of managing stress" that focuses on building awareness and coping with that specific area of mental stress, such as de-escalating stress, mind-body connection, strong emotions, negative self-talk, and how events are interpreted.

    Behavioral: Mindfulness

  • Experimental
    Social Media Reduction + Exercise

    Participants will reduce social media use by at least 30 minutes daily for two weeks. Simultaneously, participants will exercise at least 30 minutes daily. Participants are given examples of common exercises (walking, yoga, strength training, etc.), but are allowed to choose any type, although dissuaded from activities with high potential for injury.

    Behavioral: Social Media Reduction · Behavioral: Exercise

Interventions

  • BehavioralMindfulness

    15 minute daily guided meditation

  • BehavioralSocial Media Reduction

    Reduce social media use at least 30 minutes daily and exercise instead

  • BehavioralExercise

    Participants will exercise at least 30 minutes daily. Participants are given examples of common exercises (walking, yoga, strength training, etc.), but are allowed to choose any type, although dissuaded from activities with high potential for injury.

06

What researchers measure

Primary outcomes

  1. Change in Depression, Anxiety and Stress Scale - 21 (DASS-21)

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

    Time frame: baseline, immediately post intervention, post intervention up to one week

  2. Change in World Health Organization Quality of Life (WHOQoLBREF) scale

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

    Time frame: baseline, immediately post intervention, post intervention up to one week

  3. Change in smartphone screen time (minutes) for social media use

    Past-week amount of screen time for social media use

    Time frame: baseline, immediately post intervention, post intervention up to one week

  4. Change in number of social media use smartphone pick-ups

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

    Time frame: baseline, immediately post intervention, post intervention up to one week

  5. Change in percent of time using social media

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

    Time frame: baseline, immediately post intervention, post intervention up to one week

  6. Change in social media use notifications received

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

    Time frame: baseline, immediately post intervention, post intervention up to one week

Secondary outcomes

  1. Change in University of California, Los Angeles 3-Item Loneliness Scale

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

    Time frame: baseline, immediately post intervention, post intervention up to one week

  2. Change in The Gratitude Questionnaire, 6-item form (GQ-6) scale

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

    Time frame: baseline, immediately post intervention, post intervention up to one week

  3. Change in Motivations for Electronic Interaction Scale (MEIS)

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

    Time frame: baseline, immediately post intervention, post intervention up to one week

  4. Change in Comprehensive Assessment of Acceptance and Commitment Therapy Processes (CompACT-15)

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

    Time frame: baseline, immediately post intervention, post intervention up to one week

  5. Change in Bergen Social Media Addiction Scale (BSMAS)

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

    Time frame: baseline, immediately post intervention, post intervention up to one week

  6. Change in Fear of Missing Out Scale

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

    Time frame: baseline, immediately post intervention, post intervention up to one week

  7. Change in hours spent socializing inperson with peers

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

    Time frame: baseline, immediately post intervention, post intervention up to one week

  8. Change in number of evenings of past-week recreation

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

    Time frame: baseline, immediately post intervention, post intervention up to one week

07

Study locations

1 of 1 sites recruiting
  • Johns Hopkins University
    Baltimore, Maryland 21218, United States
    Recruiting
08

References and documents

Individual participant data

Plan to share: Yes — Data and other resources will be shared upon reasonable request.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 17, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07097545
Lead sponsor
Johns Hopkins Bloomberg School of Public Health
Responsible party
Sponsor
First posted
Jul 31, 2025
Start date
Aug 24, 2025
Primary completion
Dec 2026 (estimated)
Completion
Jan 2027 (estimated)
Last update
Dec 17, 2025

Study contacts

Johannes Thrul, PhD
Contact
jthrul@jhu.edu
(443) 318-6633‬
Johannes Thrul, PhD
principal investigator · Johns Hopkins University

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

Contact study team

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion