Skip to main content
Clinical Trials/NCT03707197
NCT03707197
Completed
Not Applicable

The Impact of 8 Weeks of a Digital Meditation Application on Stress-Induced Eating

University of California, Los Angeles1 site in 1 country943 target enrollmentOctober 15, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Stress-induced Eating
Sponsor
University of California, Los Angeles
Enrollment
943
Locations
1
Primary Endpoint
Reductions in perceived stress as measured by the Perceived Stress Scale
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

The aim of this study is to test the effects of a digital meditation intervention in a sample of UCLA employees who report mild to moderate stress. We will randomize University of California Los Angeles employees to either 8-weeks of a digital meditation intervention (using the commercially available application Headspace) or a waitlist control condition.

Detailed Description

The aim of this study is to test the effects of a digital meditation intervention in a sample of UCLA employees who report mild to moderate stress. UCLA employees will be randomized to either 8-weeks of a digital meditation intervention (using the commercially available application Headspace) or a waitlist control condition. Participants who are assigned to the intervention group will be asked to download and use the Headspace mobile application for at least 10 minutes per day for 8 weeks. All participants will be asked to fill out short (no longer than 25 minutes) questionnaires at baseline, week 4, week 8 (post intervention), and a 4-month follow up period. Among participants who are randomized to the digital meditation intervention, they will also take part in a 1-year follow up. All activities will take place online (via computer or smartphone). Prior to randomization, participants will complete an eligibility screening and complete the baseline questionnaire battery. The entirety of the study is digital and there are no in-person assessments. Adherence will be tracked remotely. The goal is to recruit as many as 1000 participants (500 per condition).

Registry
clinicaltrials.gov
Start Date
October 15, 2018
End Date
September 11, 2020
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

A. Janet Tomiyama

Principal Investigator

University of California, Los Angeles

Eligibility Criteria

Inclusion Criteria

  • Have access to a smartphone or computer everyday
  • Are fluent in English
  • Are a University of California, Los Angeles employee
  • Report mild to moderate levels of stress
  • Consent: demonstrate understanding of the study and willingness to participate as evidenced by voluntary informed consent and has received a signed and dated copy of the informed consent
  • Are at least 18 years of age

Exclusion Criteria

  • You may not join if you are an experienced meditator or have participated in a formal meditation practice in the last 6 months (defined as once or more per week for a duration of 20 minutes or more at each practice)

Outcomes

Primary Outcomes

Reductions in perceived stress as measured by the Perceived Stress Scale

Time Frame: Baseline to post-intervention (8 weeks from baseline)

Changes in the Perceived Stress Scale (range: 1-40; Cohen, Kamarck, \& Mermelstein, 1988). Higher scores indicate greater psychological distress.

Secondary Outcomes

  • Reductions in reward-based eating as measured by the Reward-based Eating Drive(Baseline to post-intervention (8 weeks from baseline))
  • Reductions in stress-induced eating as measured by the Palatable Eating Motives Scale(Baseline to post-intervention (8 weeks from baseline))

Study Sites (1)

Loading locations...

Similar Trials