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NCT03196999 · ClinicalTrials.gov registry record · NA
Remotely Resolving Psychological Stress (Remote RePS)
A NA study of Post Traumatic Stress Disorder, sponsored by University of California, San Francisco.
- Completed
- Registry status
- NA
- Development phase
- 528
- Enrollment target
- 1
- Study location
NCT03196999 is a NA study of Post Traumatic Stress Disorder that has completed, run by University of California, San Francisco. The registered enrollment target is 528 participants, below the 1,113-participant average among 144 other Post Traumatic Stress Disorder trials with a reported enrollment target (53% lower). The trial reports 1 study location across 1 state.
The verdict
NCT03196999, a NA study of Post Traumatic Stress Disorder, has completed, sponsored by University of California, San Francisco.
- COMPLETED
- Registry status
- NA
- Development phase
- 528 participants
- Enrollment target
- 1
- Study location
Study Summary
The investigators have developed a mobile app called Resolving Psychological Stress (REPS) for people with posttraumatic stress disorder (PTSD). The app will administer threat-related attention bias modification to individuals who score high on a PTSD checklist. This study will be administered remotely to individuals in the United States. The aims of the study are to explore feasibility, acceptability and usability of the app in an entirely remote study, as well as to explore the efficacy of the app at reducing attention bias and PTSD symptom severity.
Conditions Studied
Interventions
- BEHAVIORAL Personalized Attention Bias Training
- BEHAVIORAL Neutral Attention Training Condition
- BEHAVIORAL Non-Personalized Attention Bias Training
Study Locations (1)
California
- University of California, San Francisco - San Francisco
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 528 participants |
| Start Date | 2017-11-30 |
| Est. Completion | 2018-11-01 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03196999
The ClinicalTrials.gov registry entry for NCT03196999 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 528 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 1,113-participant average among 144 other Post Traumatic Stress Disorder trials with a reported enrollment target (53% lower). The listed sponsor is University of California, San Francisco, which has 1,713 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Post Traumatic Stress Disorder appearing as the primary indexed condition, and to 3 interventions - of which Personalized Attention Bias Training is the first listed.
NCT03196999 reports 1 study location spanning 1 distinct geographic area - top geographies include California.
Frequently Asked Questions
What is clinical trial NCT03196999 about?
NCT03196999 is a clinical study titled "Remotely Resolving Psychological Stress (Remote RePS)". The investigators have developed a mobile app called Resolving Psychological Stress (REPS) for people with posttraumatic stress disorder (PTSD). The app will administer threat-related attention bias modification to individuals who score high on a PTSD checklist. This study will be administered remot...
What is the current status of trial NCT03196999?
This trial is currently completed. It is a NA study. The enrollment target is 528 participants. The study started on 2017-11-30. Estimated completion is 2018-11-01.
What conditions does trial NCT03196999 study?
This clinical trial studies the following conditions: Post Traumatic Stress Disorder.
What interventions are being tested in trial NCT03196999?
The interventions under investigation include: Personalized Attention Bias Training (BEHAVIORAL), Neutral Attention Training Condition (BEHAVIORAL), Non-Personalized Attention Bias Training (BEHAVIORAL).
Who is sponsoring clinical trial NCT03196999?
This trial is sponsored by University of California, San Francisco, which has 1,713 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03196999 being conducted?
This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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