Chronic Pain Clinical Trial
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
Verified date | March 2019 |
Source | University of Pittsburgh |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
Status | Completed |
Enrollment | 64 |
Est. completion date | February 15, 2019 |
Est. primary completion date | December 20, 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility |
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 |
Country | Name | City | State |
---|---|---|---|
United States | UPMC Mercy Hospital | Pittsburgh | Pennsylvania |
United States | UPMC Presbyterian Hospital | Pittsburgh | Pennsylvania |
Lead Sponsor | Collaborator |
---|---|
University of Pittsburgh | Palo Alto Veteran's Institute for Research |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | PTSD Checklist for DSM 5 (Diagnostic and Statistical Manual for Mental Disorders-5) | PTSD symptoms | past 30-days | |
Secondary | Short Form of the Patient Reported Outcomes Measurement Information System (PROMIS) Pain Interference Scale | 8-items assessing pain interference | 7-days | |
Secondary | Short Form of the PROMIS Pain Intensity Scale | 3-items assessing pain intensity | 7-days |
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