Effect of a Week-long Social Media Abstention on Sustained Attention Functions

Sponsor
New York Institute of Technology (Other)
Overall Status
Recruiting
CT.gov ID
NCT06114017
Collaborator
(none)
50
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Study Details

Study Description

Brief Summary

The current study's goal is to determine if a one-week break from social media in all forms has a beneficial effect on people's attention, as measured by the Sustained Attention to Response Task, executive function as measured by the Stroop test, and well-being.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Social Media Abstention
N/A

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 Design

Study Type:
Interventional
Anticipated Enrollment :
50 participants
Allocation:
Randomized
Intervention Model:
Single Group Assignment
Intervention Model Description:
Randomized experimental and control groupRandomized experimental and control group
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Effect of a Week-long Social Media Abstention on Sustained Attention Functions
Anticipated Study Start Date :
Nov 1, 2023
Anticipated Primary Completion Date :
Mar 1, 2024
Anticipated Study Completion Date :
May 1, 2024

Arms and Interventions

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.

Behavioral: Social Media Abstention
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.

Outcome Measures

Primary Outcome Measures

  1. Inquisit Sustained Attention to Response Task (SART) [through study completion, an average of one week]

    A 6-minute computerized measure of attention.

Secondary Outcome Measures

  1. Inquisit Stroop Test [through study completion, an average of one week]

    A 5-minute measure of executive functions.

  2. Warwick-Edinburgh Mental Wellbeing Scale [through study completion, an average of one week]

    A self-report measure of general wellbeing

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 30 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 NYIT Old Westbury New York United States 11568

Sponsors and Collaborators

  • New York Institute of Technology

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Amber Sousa, Assistant Professor, New York Institute of Technology
ClinicalTrials.gov Identifier:
NCT06114017
Other Study ID Numbers:
  • BHS-1894
First Posted:
Nov 2, 2023
Last Update Posted:
Nov 2, 2023
Last Verified:
Oct 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Amber Sousa, Assistant Professor, New York Institute of Technology

Study Results

No Results Posted as of Nov 2, 2023