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Mobile Web App for Post-Traumatic Stress Disorder

N/A
Waitlist Available
Led By Nicole Short, PhD
Research Sponsored by University of North Carolina, Chapel Hill
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up change from six weeks and six months
Awards & highlights

Study Summary

This trial tests a smartphone app to help prevent and reduce posttraumatic stress in women who have survived sexual assault.

Eligible Conditions
  • Post-Traumatic Stress Disorder

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~one week, six weeks, six months
This trial's timeline: 3 weeks for screening, Varies for treatment, and one week, six weeks, six months for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Change from Baseline to Week 6 in ASI Scores
Change from Week 6 to Month 6 in PCL-5 Scores
Change from Week 6 to Month 6 in PROMIS Anxiety Scores
+2 more
Secondary outcome measures
Association between Change in General Health and Anxiety Sensitivity
Insomnia Severity Index Scores
Somatic Symptoms

Trial Design

1Treatment groups
Experimental Treatment
Group I: App InterventionExperimental Treatment1 Intervention
All participants will receive the web app for prevention of posttraumatic stress.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Mobile Web App
2020
N/A
~30

Find a Location

Who is running the clinical trial?

University of North Carolina, Chapel HillLead Sponsor
1,506 Previous Clinical Trials
4,190,536 Total Patients Enrolled
Nicole Short, PhDPrincipal InvestigatorUniversity of Nevada, Las Vegas
Samuel McLean, MD, MPHPrincipal InvestigatorUniversity of North Carolina, Chapel Hill
1 Previous Clinical Trials
41 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Recent research and studies
eGEMs (Generating Evidence & Methods to improve patient outcomes)Journal
Advances in Patient Reported Outcomes: The NIH PROMIS Measures
Broderick, Joan, Esi Morgan DeWit, Nan Rothrock, Paul Crane, and Christopher B. Forrest. 2013. “Advances in Patient Reported Outcomes: The NIH PROMIS Measures”. Egems (generating Evidence & Methods to Improve Patient Outcomes). Ubiquity Press, Ltd.. doi:10.13063/2327-9214.1015.
clinicaltrials.govStudy
Testing of a Mobile Web App to Decrease Posttraumatic Stress Symptoms in Women After Sexual Assault
2020. "Testing of a Mobile Web App to Decrease Posttraumatic Stress Symptoms in Women After Sexual Assault". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT04334356.
~5 spots leftby Apr 2025
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