- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06114017
Effect of a Week-long Social Media Abstention on Sustained Attention Functions
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
50 participants between the ages of 18 and 30 years will be recruited for the study via fliers and word of mouth. Following consent procedures, those who choose to participate will be randomized to intervention or control. 25 will be randomly selected to be in the social media group and the other 25 will be selected to go 1 week without engaging with or viewing social media to the best of their ability.
All participants will complete a demographic form at baseline and a survey about their use of social media, as well as the Bergen Social Media Assessment Scale, and the Warwick-Edinburgh Mental Wellbeing Scale. Following that, they will complete the Stroop and the SART, described below. All 50 of them will be asked to take the SART and Stroop (Inquisit Millisecond versions) tests to obtain baseline attention and executive functioning measures. Temporary deletion of social media apps will be supervised by an investigator. Subjects will be given a daily brief report/log to record any use of social media through Redcap. At the end of the week a repeat SART, Stroop, and Warwick-Edinburgh Mental Wellbeing scale will be re-administered. The group that deleted their social media will then be able to redownload their social media if they so choose. A survey about their subjective experience at the conclusion of the week will then be given to all subjects.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Amber Sousa, PhD
- Phone Number: 516-686-7698
- Email: asousa@nyit.edu
Study Contact Backup
- Name: Alec Toufexis
- Phone Number: 516-686-7698
- Email: atoufe01@nyit.edu
Study Locations
-
-
New York
-
Old Westbury, New York, United States, 11568
- Recruiting
- NYIT
-
Contact:
- Amber Sousa, PhD
- Phone Number: 631-686-7698
- Email: asousa@nyit.edu
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- 18-30 years old
- have and regularly use some form of social media
- use on average more than 1 hour of social media a day
- are willing to temporarily delete all social media for 1 week duration
Exclusion Criteria:
- no social media usage
- ADHD or other known conditions that affect attention and/or concentration
- current concussion
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: 1: Social Media Abstention
People in this arm will be encouraged to disable social media and not use social media for one week.
|
People will stop or reduce their social media use for one week.
|
|
No Intervention: 2: Control
People in this group will continue their normal behavior in regard to social media use.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Inquisit Sustained Attention to Response Task (SART)
Time Frame: through study completion, an average of one week
|
A 6-minute computerized measure of attention.
|
through study completion, an average of one week
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Inquisit Stroop Test
Time Frame: through study completion, an average of one week
|
A 5-minute measure of executive functions.
|
through study completion, an average of one week
|
|
Warwick-Edinburgh Mental Wellbeing Scale
Time Frame: through study completion, an average of one week
|
A self-report measure of general wellbeing
|
through study completion, an average of one week
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- BHS-1894
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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