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NOT YET RECRUITING
NCT07812506
NA

Social Media Withdrawal in Pregnancy: Effects on Maternal Mental Health and Misinformation

Sponsor: Massachusetts General Hospital

View on ClinicalTrials.gov

Summary

The goal of this clinical trial is to learn if restricting social media use with a hardware device can improve mental health and well-being during pregnancy. It will also learn about the feasibility and acceptability of this approach. The main questions it aims to answer are: * Does restricting social media use lower the amount of time participants spend on social media? * Does restricting social media use improve depression, anxiety, well-being, loneliness, sleep, and physical activity? Researchers will compare participants who use a device (Brick™) that restricts social media apps to participants receiving usual care to see if the device improves social media use and mental health outcomes. Participants will: * Complete surveys about mood, sleep, and social media use, and wear/carry a smartphone app that tracks activity and sleep * Use the Brick device to restrict social media apps for 2 weeks, or continue their usual phone use * Complete follow-up surveys at the end of the 4-week study

Official title: SWIPE LEFT: Social Media Withdrawal in Pregnancy - Effects on Maternal Mental Health and Misinformation

Key Details

Gender

FEMALE

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

70

Start Date

2026-10-01

Completion Date

2027-12

Last Updated

2026-09-10

Healthy Volunteers

Yes

Conditions

Interventions

DEVICE

Brick device

A hardware-based device that restricts access to user-selected social media applications by requiring physical interaction with the device to unlock them. Participants in the intervention arm will use the device continuously to block access to selected social media apps during a 2-week intervention period, following a 2-week baseline monitoring period. The device is not an FDA-regulated medical device and functions as a consumer hardware tool. Participants may voluntarily reverse the intervention (unlock the device) at any point during the study.

Locations (1)

Massachusetts General Hospital

Boston, Massachusetts, United States