Mission Reconnect-Veterans and Their Partners to Manage Pain and PTSD (MR)
- Conditions
- PTSDChronic Musculoskeletal Pain
- Registration Number
- NCT03593772
- Lead Sponsor
- VA Office of Research and Development
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 730
Inclusion Criteria:<br><br> - English-speaking Veterans with chronic musculoskeletal pain.<br><br> - Veteran is considered to have chronic musculoskeletal pain if he or she meeting<br> either of two validated criteria:<br><br> - (1) Having 2+ occurrences of any of targeted musculoskeletal ICD-9-CM codes<br> likely to represent chronic pain recorded at visits separated by at least 30<br> days within past six months<br><br> - (2) Having high impact chronic pain = 2+ occurrences of targeted<br> musculoskeletal ICD-9-CM codes separated by at least 30 days within the past<br> six months previous to study recruitment and two or more pain scores greater<br> than or equal to 4 separated by at least 30 days within past six months.<br><br> - For pain scores, the investigators will use the 0-10 numeric pain rating scale that<br> is routinely collected at the VA.<br><br> - The investigators will count two ICD-9-CM codes or pain scores recorded on the<br> same day as one code/score.<br><br> - Veteran is considered to have PTSD if he or she has a flag in his/her record<br> indicating confirmed condition by the VA Compensation and Benefits program, has<br> at least two outpatient visits in the year with the primary diagnosis being<br> listed as PTSD (ICD-9-CM code 309.81) and/or had PTSD listed on the problem<br> list], Veteran must also have PTSD (defined by PTSD diagnosis-ICD-9-CM 309.81),<br> the ability to access and use an electronic platform (e.g. Mobile device,<br> internet, DVD) for MR delivery, with a willing partner to also participate in<br> the study and MR program.<br><br>Exclusion Criteria:<br><br> - Moderate to severe traumatic brain injury (TBI)<br><br> - Diagnosis or documented treatment for psychosis in previous 6 months<br><br> - Currently in substance use disorder treatment<br><br> - Non-English speaking<br><br> - Visual, hearing, cognitive impairment that prevent participation or ability to<br> consent<br><br> - And/or lack of access to internet service<br><br> - These individuals will be excluded due to medical, language, and technology access<br> issues that would prevent safe and full study participation.<br><br> - Pain and PTSD treatment will not be factored as an inclusion/exclusion criteria but<br> will be evaluated as covariates.<br><br> - Potential participants who screen for aggression or violence will also be excluded<br> from study.
Not provided
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain Outcomes Questionnaire (POQ)
- Secondary Outcome Measures
Name Time Method Pain, Stress and Tension Likert;Defense and Veterans Pain Rating Scale;PTSD: Posttraumatic Checklist;Quality of Life Short-form (SF12);Sleep Quality: Pittsburgh Sleep Quality Index (PSQI);Compassion for Self and Others Scales