Daily Assessment of Mood and Social Media Behaviors Study

January 24, 2022 updated by: Southern Methodist University
The purpose of this research study is to learn more about social media usage and its relation to emotions, biology, and mental health. Participants will complete daily assessments (5 times a day) over the course of 11 days in which they will report on their social media use, behaviors, and mood. During the first 4 days participants will be asked to continue using social media as typical. In the second half (7 days) participants will be randomized to social media usage groups (0 minutes, 30 minutes, 1 hour, 2 hour, 3 hours). There will be mental health and well-being measures provided at the beginning and end of the study. Lastly, to better understand how social media usage effects underlying mechanisms of stress, participants will be asked to provide saliva samples for 3 nights (pre, mid, and post) to assess for basal cortisol levels.

Study Overview

Status

Completed

Study Type

Interventional

Enrollment (Actual)

324

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Texas
      • Dallas, Texas, United States, 75205
        • Southern Methodist University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Having a smartphone

Exclusion Criteria:

  • Below age of 18

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: No Social Media Use
Participants will be asked to refrain from using all social media
Behavioral Intervention of social media usage.
Experimental: Maximum 30 minutes of use
Participants will be asked to only use social media at most 30 minutes a day.
Behavioral Intervention of social media usage.
Experimental: Maximum 1 hour of use
Participants will be asked to only use social media at most 60 minutes a day.
Behavioral Intervention of social media usage.
Experimental: Control
Control Group
Behavioral Intervention of social media usage.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Changes in "Positive and Negative Affect Schedule" (PANAS)
Time Frame: Pre and post. Daily 5 times a day for 11 days
Examines mood fluctuations. Scores can range from 10-50 for both the Positive and Negative Affect with the lower scores representing lower levels of Positive/Negative Affect and higher scores representing higher levels of Positive/Negative Affect.
Pre and post. Daily 5 times a day for 11 days
Changes in "Depression Anxiety and Stress Scale" (DASS)
Time Frame: Pre and Post. Daily for 11 days
Examines Depressive, Anxiety, and Stress symptoms. Minimum 0 maximum 63. Higher scores indicate more depression, anxiety and or stress.
Pre and Post. Daily for 11 days
Changes in "Behavioral Activation for Depression Scale"
Time Frame: Pre-Post- Daily for 11 days
Examines behavioral goal achievement. Minimum 0 and maximum 54. Larger scores means an ability to be more active.
Pre-Post- Daily for 11 days
Changes in "Social Media Use"
Time Frame: Daily for 11 days
Survey and Phone based Applications will assess for daily use of social media time and behaviors.
Daily for 11 days
Changes in "A clinically useful depression outcome scale" (CUDOS)
Time Frame: Pre-Post- Daily for 11 days
Tracks Depression Symptoms. Minimum 0 maximum 74. Larger scores means more depressive symptoms.
Pre-Post- Daily for 11 days

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 1, 2020

Primary Completion (Actual)

May 1, 2021

Study Completion (Actual)

May 1, 2021

Study Registration Dates

First Submitted

February 19, 2020

First Submitted That Met QC Criteria

April 14, 2020

First Posted (Actual)

April 16, 2020

Study Record Updates

Last Update Posted (Actual)

February 8, 2022

Last Update Submitted That Met QC Criteria

January 24, 2022

Last Verified

January 1, 2022

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • H19-131-ROQA

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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.

Clinical Trials on Depression

Clinical Trials on Social Media Usage Manipulation

Subscribe