The Mobile PTSD Coach App in Acute Injury Survivors

Sponsor
University of Pittsburgh (Other)
Overall Status
Completed
CT.gov ID
NCT03247179
Collaborator
Palo Alto Veterans Institute for Research (Other)
64
2
2
16.9
32
1.9

Study Details

Study Description

Brief Summary

This project is a preliminary randomized controlled trial testing the potential impact of the PTSD Coach mobile application at reducing posttraumatic stress and pain symptoms among acutely injured trauma patients. Immediately following the injury, patients will be randomly assigned to use the PTSD Coach app, or to the treatment as usual condition.

Condition or Disease Intervention/Treatment Phase
  • Other: PTSD Coach mobile application
N/A

Detailed Description

Traumatic injury is the leading cause of mortality in the U.S. for young people, and a source of long-term morbidity in all ages. A majority of trauma patients report chronic pain (CP) and disability at 4-months (30%- 79%) and 12-months (63%) post-injury. Maladaptive psychological processes have a stronger association with the transition to CP than does injury severity. Posttraumatic stress disorder (PTSD) symptoms (e.g., intrusions, avoidance and hyperarousal) occur in up to 22% of post-injury patients and herald the transition from acute to CP. Although psychological interventions can modify PTSD symptoms, and reduce CP, it is unknown if early intervention to prevent PTSD symptoms can prevent post-injury CP altogether. "PTSD Coach" is a publicly available, free, mobile app that provides scalable and psychosocial support modeled on principles of cognitive-behavioral therapy. PTSD Coach has helped Veterans and civilians to manage PTSD.

This project will test whether PTSD Coach can reduce post-injury maladaptive psychological processes and thereby prevent post-injury CP. The preventive intervention will be targeted towards those at the highest-risk of developing PTSD.

The investigators propose to test the efficacy of the PTSD Coach app vs. treatment as usual (TAU) among a sample of acute physical injury patients, to: 1) Determine engagement with PTSD Coach, by measuring frequency of use over 4-weeks and assessing ratings of usefulness and qualitative feedback: it is expected that >80% of PTSD Coach users will use the app at least once a week, and will rate it as at least somewhat helpful; 2) Estimate effect on CP symptoms by measuring PTSD and pain intensity at 1- and 3-months. The effect of the intervention on pain interference, disability, and coping self-efficacy will also be explored.

Study Design

Study Type:
Interventional
Actual Enrollment :
64 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Participants will be randomly assigned to either the experimental condition (PTSD Coach app usage), or the treatment as usual condition.Participants will be randomly assigned to either the experimental condition (PTSD Coach app usage), or the treatment as usual condition.
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Secondary Prevention With the Mobile PTSD Coach App to Improve Health Outcomes and the Continuity of Care Following Traumatic Physical Injury: A Randomized Controlled Trial
Actual Study Start Date :
Sep 19, 2017
Actual Primary Completion Date :
Dec 20, 2018
Actual Study Completion Date :
Feb 15, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: PTSD Coach Condition

PTSD Coach App

Other: PTSD Coach mobile application
The PTSD Coach app is publicly available for free, and draws on cognitive behavioral therapy components to help participants learn, manage, and cope with their PTSD symptoms in real time.

No Intervention: Treatment as Usual Condition

Treatment as Usual

Outcome Measures

Primary Outcome Measures

  1. PTSD Checklist for DSM 5 (Diagnostic and Statistical Manual for Mental Disorders-5) [past 30-days]

    PTSD symptoms

Secondary Outcome Measures

  1. Short Form of the Patient Reported Outcomes Measurement Information System (PROMIS) Pain Interference Scale [7-days]

    8-items assessing pain interference

  2. Short Form of the PROMIS Pain Intensity Scale [7-days]

    3-items assessing pain intensity

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • English-speaking adults seeking treatment in the ED

  • Adults between the ages of 18-65

  • Sustained a musculoskeletal injury (e.g., fractures, sprains or strains, contusions, dislocations, crushing injuries and open wounds; and other chief complains involving the neck, back, or extremities)

  • Injury resulting from a motor vehicle crash (MVC) or motorcycle crash (MCC) that occurred within the past 24 hours

  • Eligible patients must own a mobile phone with short-message service (SMS) features (e.g., the ability to send and respond to text messages) and the ability to download apps

  • Participants must self-report that they experienced a potential traumatic event reflected by Criterion A of the DSM-5 PTSD diagnosis (endorse actual or perceived life threat and/or serious injury141,142)

  • Participants must self-report that they experienced a painful injury reflected by a pain score ≥4 using the verbal numerical score (0-10) in response to the question: "On a scale of 0-10, how severe is your pain?"

  • Patients with a past history of PTSD, but not currently receiving treatment (e.g., benzodiazepines or mental/behavioral therapy), are eligible for participation.

Exclusion Criteria:
  • Presenting to the ED for a non-MVC/MCC (i.e., fall, assault)

  • Participants who do not own a mobile phone with SMS features

  • Participants with a pain score < 4 or do not endorse Criterion A of the DSM-5 PTSD diagnosis

  • Spinal injuries

  • Major lacerations resulting in significant damage to subcutaneous tissue (e.g., degloving) and specific nerve injury (these injuries could lead to a distinct neuropathic pain syndrome)

  • Traumatic brain injury; Evidence of moderate to severe cognitive impairment secondary to trauma-related head injury (GCS<13)

  • Self-inflicted injury

  • Time since trauma > 24 hours

  • Non-English speaking; younger than 18 or older than 65

  • Not medically stable or alert and oriented

  • Initiation of benzodiazepines and other psychotropic medications at time of ED visit

  • Initiation of mental or behavioral health therapy at time of ED visit

  • Currently enrolled in treatment (medication or mental/behavioral health therapy) for PTSD

  • Prisoners

Contacts and Locations

Locations

Site City State Country Postal Code
1 UPMC Presbyterian Hospital Pittsburgh Pennsylvania United States 15213
2 UPMC Mercy Hospital Pittsburgh Pennsylvania United States 15219

Sponsors and Collaborators

  • University of Pittsburgh
  • Palo Alto Veterans Institute for Research

Investigators

  • Principal Investigator: Maria L Pacella, PhD, University of Pittsburgh

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Maria Pacella, Research Assistant Professor, University of Pittsburgh
ClinicalTrials.gov Identifier:
NCT03247179
Other Study ID Numbers:
  • PRO16010595
First Posted:
Aug 11, 2017
Last Update Posted:
Mar 4, 2019
Last Verified:
Mar 1, 2019
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 4, 2019