MedPath

Mission Reconnect-Veterans and Their Partners to Manage Pain and PTSD (MR)

Not Applicable
Completed
Conditions
PTSD
Chronic 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

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.

Exclusion Criteria

Not provided

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain Outcomes Questionnaire (POQ)
Secondary Outcome Measures
NameTimeMethod
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
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