- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02445196
PTSD Coach App Evaluation
Study Overview
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Experienced or witnessed an extremely traumatic event that involved actual or threatened death or serious injury to you or someone else. Event must have occurred more than 1 month ago.
- Significant PTSD symptoms. Total PTSD Checklist Score ≥ 35.
- Have a smartphone or smart device that can download apps (iPhone, iPod touch, iPad, or android phone or tablet).
- English is the primary language.
- Available for the next 6 months to participate in the study and use smart device.
Exclusion Criteria:
- Unable to give informed consent.
- Is currently receiving mental health treatment.
- Currently participating in other PTSD-related research studies
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: PTSD Coach
Subjects assigned to this condition receive information about how to download the research app, PTSD Explorer.
This research version of PTSD Coach functions exactly the same, however we have the ability to track individual usage of the app.
The app contains contains psycho-education about PTSD and the management of symptoms of PTSD along with activities and techniques to address symptoms.
Subjects are told to use the app as much or as little as they want over the next three months.
|
PTSD Coach is a mobile app that aims to teach individuals self-management strategies for symptoms of PTSD.
All participants must have a smartphone, either apple or android.
|
|
Active Comparator: Waitlist Control
Subjects assigned to this condition are told: "You have been randomly assigned to Group 2, the group that does not use the app." Following their completion of the post-intervention assessment at 3 months, they are told how to access to the publicly available PTSD Coach app in the Apple App Store or Android Play Store, just so that they are made aware of the resources available to them. |
PTSD Coach is a mobile app that aims to teach individuals self-management strategies for symptoms of PTSD.
All participants must have a smartphone, either apple or android.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in PTSD Symptoms Measured by the Post Traumatic Stress Disorder Checklist (PCL)
Time Frame: Baseline to Posttreatment (3 months)
|
PTSD symptoms were assessed with the PCL-C (Weathers et al., 1993), a 17-item self-report measure of DSM-IV PTSD symptoms with strong psychometric properties (Wilkins, Lang, & Norman, 2011).
Items are rated on how much the symptom bothered the respondent in the past month on a scale ranging from 1 (not at all) to 5 (extremely), with the sum score ranging from 17 to 85 providing a symptom severity rating, with higher ratings indicating more severe PTSD symptoms.
|
Baseline to Posttreatment (3 months)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Subject Coping Self-efficacy Measured by a Questionnaire Assessing Confidence in Managing Core Symptoms of PTSD Addressed in the Intervention
Time Frame: Baseline to Posttreatment (3 months)
|
PTSD symptom coping SE was assessed with a 9-item self-report measure developed for the study following Bandura's guidelines (Bandura, 2006).
Items assess confidence in managing PTSD symptoms and reaching out for support on a scale from 0 (cannot do at all) to 100 (highly certain can do).
The average score provides an overall measure of SE with higher scores reflecting greater self-efficacy coping with PTSD symptoms.
Cronbach's alpha at baseline was .87.
|
Baseline to Posttreatment (3 months)
|
|
Change in Interpersonal Functioning Measured by a Brief Inventory of Psychosocial Functioning (IPF7)
Time Frame: Baseline to Posttreatment (3 months)
|
Psychosocial functioning was measured using the Brief Inventory of Psychosocial Functioning (B-IPF; Erb, Kearns, Bovin et al., 2015), a 7-item self-report measure.
Items are rated on how much trouble the respondent had in the past month in relationships or other important areas of functioning (e.g., work, training or education) on a scale ranging from 0 (not at all) to 6 (very much).
An average of applicable items provides an index of psychosocial functioning, with higher scores reflecting more poorer psychosocial functioning.
Cronbach's alpha at baseline was .82.
|
Baseline to Posttreatment (3 months)
|
|
Change in Depression Symptoms Measured by the Patient Health Questionnaire (PHQ8)
Time Frame: Baseline to Posttreatment (3 months)
|
Depression was assessed with the Patient Health Questionnaire depression scale (PHQ-8; Kroenke et al., 2009), an 8-item self-report measure of depression with evidence showing its ability to measure depression symptom severity and potential diagnosis.
Items are rated on how much the symptom bothered the respondent in the past two weeks on a scale ranging from 0 (not at all) to 3 (nearly every day).
Total scores can range from 0 to 24, with higher scores indicating more severe depression symptoms.
Cronbach's alpha at baseline was .87.
|
Baseline to Posttreatment (3 months)
|
|
Sustained Change in PTSD Symptoms Measured by the Post Traumatic Stress Disorder Checklist (PCL)
Time Frame: Postreatment to 3-month Follow-up
|
PTSD symptoms were assessed with the PCL-C (Weathers et al., 1993), a 17-item self-report measure of DSM-IV PTSD symptoms with strong psychometric properties (Wilkins, Lang, & Norman, 2011).
Items are rated on how much the symptom bothered the respondent in the past month on a scale ranging from 1 (not at all) to 5 (extremely), with the sum score ranging from 17 to 85 providing a symptom severity rating, with higher ratings indicating more severe PTSD symptoms.
|
Postreatment to 3-month Follow-up
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: C Barr Taylor, M.D., Stanford University
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 22977
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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