Johns Hopkins University
Baltimore, Maryland, 21218, United States
Location status: Recruiting
NCT Number: NCT07097545
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).
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Not applicable
Baltimore, Maryland, 21218, United States
Location status: Recruiting
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.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
1 hour)
Exclusion criteria
15 minute daily guided meditation
Reduce social media use at least 30 minutes daily and exercise instead
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.
Time frame: baseline, immediately post intervention, post intervention up to one week
Score range = 0-63, higher score = worse outcome
Time frame: baseline, immediately post intervention, post intervention up to one week
Score range = 13-65, lower score = worse outcome
Time frame: baseline, immediately post intervention, post intervention up to one week
Past-week amount of screen time for social media use
Time frame: baseline, immediately post intervention, post intervention up to one week
Past-week total number of smartphone pickups for social media use applications
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.
Time frame: baseline, immediately post intervention, post intervention up to one week
Past-week total number of notifications received for social media use applications
Time frame: baseline, immediately post intervention, post intervention up to one week
Score range = 3-9, higher score = worse outcome
Time frame: baseline, immediately post intervention, post intervention up to one week
Score range = 6-42, lower score = worse outcome
Time frame: baseline, immediately post intervention, post intervention up to one week
Score range = 10-50, higher score = worse outcome
Time frame: baseline, immediately post intervention, post intervention up to one week
scale Score range = 0-138, lower scores = worse outcome
Time frame: baseline, immediately post intervention, post intervention up to one week
Score range = 6-35, higher score = worse outcome
Time frame: baseline, immediately post intervention, post intervention up to one week
Score range = 10-50, higher score = worse outcome
Time frame: baseline, immediately post intervention, post intervention up to one week
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
Score range = 0-7 evenings of recreation, lower scores = worse outcome
Contact information is provided by the study sponsor or research team.
Johns Hopkins Bloomberg School of Public Health
Other
Social Media Use Study
Acronym: SMUS
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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