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NCT03695627 · ClinicalTrials.gov registry record · NA
Stress Free UCR: The Impact of 8 Weeks of Headspace on Stress in a Heterogeneous University Employee Cohort
A NA study, sponsored by University of California, Riverside.
- Completed
- Registry status
- NA
- Development phase
- 165
- Enrollment target
NCT03695627: Completed NA study, sponsored by University of California, Riverside.
NCT03695627 is a NA study that has completed, run by University of California, Riverside. The registered enrollment target is 165 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (88% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT03695627, a NA study, has completed, sponsored by University of California, Riverside.
- COMPLETED
- Registry status
- NA
- Development phase
- 165 participants
- Enrollment target
Study Summary
The aim of this study is to test the effects of a digital meditation intervention in a sample of high stress UCR employees. We will randomize UCR employees to 8-weeks of either a digital mindfulness 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 10 minutes per day for 8 weeks. They will be asked to fill out short (no longer than 30 minutes long) questionnaires at baseline, week 4, week 8 (post intervention), and a 4-month follow up period. Participants who are randomized to the digital meditation intervention will also take part in a 1-year follow up. All activities will take place online (via computer or smartphone), and on the participants' own time.
Primary Outcome
The Perceived Stress Scale has a total score scale range of 0 to 40, with higher values indicating more perceived stress
Interventions
- BEHAVIORAL Meditation
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 165 participants |
| Start Date | 2018-07-13 |
| Est. Completion | 2020-06-20 |
| Phase | NA |
What the finished NCT03695627 record still lists
NCT03695627 is an interventional study that assigns participants to a tested intervention. The registered 165 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (88% lower).
The record links to 0 conditions, and to 1 intervention - of which Meditation is the first listed.
NCT03695627 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT03695627 about?
NCT03695627 is a clinical study titled "Stress Free UCR: The Impact of 8 Weeks of Headspace on Stress in a Heterogeneous University Employee Cohort". The aim of this study is to test the effects of a digital meditation intervention in a sample of high stress UCR employees. We will randomize UCR employees to 8-weeks of either a digital mindfulness intervention (using the commercially available application Headspace) or a waitlist control condition...
What is the current status of trial NCT03695627?
This trial is currently completed. It is a NA study. The enrollment target is 165 participants. The study started on 2018-07-13. Estimated completion is 2020-06-20.
What interventions are being tested in trial NCT03695627?
The interventions under investigation include: Meditation (BEHAVIORAL).
Who is sponsoring clinical trial NCT03695627?
This trial is sponsored by University of California, Riverside, which has 10 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT03695627's enrollment target sits among peer trials
165 626th of 2000 higher than 1,375 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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