Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

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: Completed NA study of Post Traumatic Stress Disorder, sponsored by University of California, San Francisco.

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 662-participant average among 262 other Post Traumatic Stress Disorder trials with a reported enrollment target (20% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

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.

Primary Outcome

To examine a usability survey in which participants rate their experience of completing attention bias modification via a mobile app. Specifically, the questions regard the acceptability, feasibility, and usability to a completely remote, clinical population.

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

FieldValue
Enrollment Target 528 participants
Start Date 2017-11-30
Est. Completion 2018-11-01
Phase NA

What the finished NCT03196999 record still lists

NCT03196999 is an interventional study that assigns participants to a tested intervention. The registered 528 participants enrollment target is mid-sized for trials with a published cap, below the 662-participant average among 262 other Post Traumatic Stress Disorder trials with a reported enrollment target (20% lower).

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 a single indexed study location in 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.

Similar trials for Post Traumatic Stress Disorder

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT03196999's enrollment target sits among peer trials

528 13th of 262 higher than 250 of 262 other Post Traumatic Stress Disorder trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Post Traumatic Stress Disorder 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT05373017 · 528 participants · NA

    Delirium and Neuropsychological Recovery Among Emergency General Surgery Survivors

  • NCT05634252 · 528 participants · Phase 3

    Undergraduate Skin Cancer Prevention Trial

  • NCT06383273 · 528 participants · Phase 3

    A Study to Evaluate Efficacy and Safety of MELT-300 for Procedural Sedation in Subjects Undergoing Cataract Extraction With Lens Replacement (CELR)

  • NCT06470243 · 528 participants · Phase 3

    Testing Whether the Addition of Carboplatin Chemotherapy to Cabazitaxel Chemotherapy Will Improve Outcomes Compared to Cabazitaxel Alone in People With Castrate-Resistant Prostate Cancer That Has Spread Beyond the Prostate to Other Parts of the Body

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT03196999, the US trial registry maintained by the National Library of Medicine. NCT03196999 (mid enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.