N/A
N=23
Intensive Treatment for Chronic Pain and Posttraumatic Stress Disorder (PTSD)
Stress Disorders, Post-Traumatic
Bottom Line
View on ClinicalTrials.gov: NCT01120067 ↗Enrolled (actual)
23
Serious AEs
0.0%
Results posted
Dec 2016
Primary outcome: Primary: McGill Pain Questionnaire — 31.91; 30.83 units on a scale
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Intensive Treatment (Behavioral); Treatment as Usual (Behavioral)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- VA Office of Research and Development
- Primary completion
- Aug 2015
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY McGill Pain Questionnaire |
31.91; 30.83 | — |
Summary
This study is investigating the efficacy of an intensive (3 week) integrated treatment for Veterans with both pain and PTSD.
Eligibility Criteria
Inclusion Criteria
- Patients will be eligible to participate if they have constant pain of at least three months duration with a neurologic or musculoskeletal etiology.
- Patients must also meet diagnostic criteria for PTSD.
Exclusion Criteria
- Patients with life threatening or acute physical illness, current alcohol or substance abuse, current psychosis or suicidal ideation, and individuals seeking pain treatment such as surgical interventions will be excluded.
Data sourced from ClinicalTrials.gov (NCT01120067). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.