Skip to main content
Clinical Trials/NCT03624348
NCT03624348
Unknown
Not Applicable

The Impact of 8 Weeks of a Digital Meditation Application on Stress and Job Strain in a Heterogeneous University Employee Cohort

University of California, Irvine1 site in 1 country2,000 target enrollmentSeptember 20, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Stress
Sponsor
University of California, Irvine
Enrollment
2000
Locations
1
Primary Endpoint
Change in perceived stress score, as determined by the total score on the Perceived Stress Scale
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 University of California, Irvine (UCI) employees who report mild to moderate stress. UCI employees will be randomized 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 UCI employees who report moderate to high stress. UCI 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 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 study 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 go through 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 2000 participants (1000 per condition).

Registry
clinicaltrials.gov
Start Date
September 20, 2018
End Date
March 2022
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • You may join if you:
  • Have access to a smartphone or computer every day
  • Are fluent in English
  • Are a UCSF 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

Change in perceived stress score, as determined by the total score on the Perceived Stress Scale

Time Frame: Baseline to post-intervention, an anticipated average of 8 weeks

The Perceived Stress Scale has a total score scale range of 0 to 40, with higher values indicating more perceived stress

Secondary Outcomes

  • Change in job overcommitment, as as determined by Siegrist Job Strain Scale(Baseline to post-intervention, an anticipated average of 8 weeks)
  • Change in work engagement, as determined by the Utrecht Work Engagement Scale(Baseline to post-intervention, an anticipated average of 8 weeks)
  • Change in job strain, as determined by Siegrist Job Strain Scale(Baseline to post-intervention, an anticipated average of 8 weeks)
  • Change in burnout, as determined by the Bergen Burnout Inventory(Baseline to post-intervention, an anticipated average of 8 weeks)
  • Change in subjective mindfulness, as determined by total score on Mindful Attention Awareness Scale(Baseline to post-intervention, an anticipated average of 8 weeks)

Study Sites (1)

Loading locations...

Similar Trials