- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02049086
Pain Management for Veterans Filing Compensation Claims (SBIRT LBP)
This proposal will develop and test an indicated prevention strategy, Screening, Brief Intervention and Referral to Treatment with Pain-Management advice (SBIRT-PM), in Veterans who have filed a claim for a (military) service-connected injury for which they have requested financial compensation. Although typically only an information-gathering, forensic-styled examination, the Compensation examination is a crucial point of entry to VA care. Objectives are:
- To finalize the procedures, manual, and training materials of SBIRT-PM. The goals of this stage will be (1) optimizing SBIRT-PM's appeal to Veterans concerned about their musculoskeletal conditions and their Compensation claims; and (2) finalizing the counseling materials and procedures.
- To conduct a randomized clinical trial comparing SBIRT-PM to a no referral arm and a pain module only arm.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Connecticut
-
West Haven, Connecticut, United States, 06516
- VA Connecticut Healthcare System (VACHS)
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Veteran of OEF/OIF/OND
- Scheduled exam for back, neck, knee, or shoulder. These four body parts were selected because they are classified as MSD by the VBA and are common causes of chronic non-cancer pain. Including other conditions (e.g. osteomyelitis, muscle injuries) would introduce more heterogeneity in illness course.
- Able to participate psychologically and physically, able to provide informed consent, complete assessments, and participate in study procedures.
- Self-reports peak pain of at least 2 on a numeric pain rating scale (0 "no pain" to 10 "worst pain imaginable" in the last 28 days in the joint that is the focus of the claim. This broad pain inclusion criterion may be narrowed after the Counseling Refinement Stage. Some Veterans apply for service connection for injuries that are not currently symptomatic, in case the injury recurs. This criterion will exclude these asymptomatic Veterans
Risky substance use within the last 28 days, defined as one of the following:
- Risky alcohol use: i.e. >14 drinks/week or>4 drinks/occasion for men 65 or younger; >7 drinks/week or >3 drinks/occasion for women. A standard drink will be 14 grams of absolute alcohol, equivalent to 12 oz of beer, 5 oz of wine, or 1.5 oz of 80-proof liquor
- Self-reported use of an illicit drug in the preceding 28 days. Use of opioids or sedative hypnotics not prescribed to the Veteran will be considered illicit drug use.Medical marijuana is legal in Connecticut but is illegal federally. Use of medical marijuana puts someone at some risk for future misuse of cannabis or other drugs and therefore will be treated as an illicit drug.
- Misuse of prescribed opioid medications in the preceding 28 days. Two questions adapted from the CIDI for use in a NIDA Clinical Trials Network study, were modified to describe misuse of prescribed opioid medications: "How often have you taken your pain medications in larger amounts than prescribed or for a longer period than prescribed?" and "How often have you used your pain medicines to get high, to relax, or to make you feel more alert?"
Exclusion Criteria:
- Will not be able to attend the follow-up appointments.
- Attended VA or non-VA substance abuse treatment during the three months prior to randomization. Veterans who are receiving mental health treatment but indicate it is not addressing substance use will be enrolled.
- Physiological dependence on alcohol, illicit drugs, or non-prescribed opioids. People with more severe dependence have not benefited from SBIRT in prior studies.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Screening
- Allocation: Randomized
- Interventional Model: Single Group Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: SBIRT-PM
Screening, Brief Intervention and Referral to Treatment with Pain-Management advice (SBIRT-PM)
|
Screening, Brief Intervention and Referral to Treatment with Pain-Management advice (SBIRT-PM)
|
|
Active Comparator: Pain Module Only
The pain module of SBIRT-PM with no substance abuse focus (Pain Module Only)
|
The pain module of SBIRT-PM with no substance abuse focus (Pain Module Only)
|
|
No Intervention: No Additional Referral
No intervention.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Risky substance use
Time Frame: baseline
|
A week will be defined as having had risky substance use if it had alcohol use at risky levels ( >14 drinks/week or 4 on an occasion for men or 7/week and >3/day for women), or illicit drug use.
Weeks will be considered positive for illicit use if there is either a positive toxicology screen or self-reported use on that week.
|
baseline
|
|
Pain
Time Frame: baseline
|
The primary pain outcome will be the pain severity score form the Brief Pain Inventory
|
baseline
|
|
Service Use
Time Frame: baseline
|
Service use will be coded for each week as whether the Veteran attended any pain related, substance abuse and/or mental health treatment.
Attendance at treatment during a week will be defined as having any service use data (VA or self-reported use of non-VA services) indicating use.
The difference in probability of attendance over time will be compared across treatment groups.
Use of non-VA services, and whether substance abuse was addressed during a counseling session will be self-reported.
|
baseline
|
|
Risky substance use
Time Frame: week 4
|
A week will be defined as having had risky substance use if it had alcohol use at risky levels ( >14 drinks/week or 4 on an occasion for men or 7/week and >3/day for women), or illicit drug use.
Weeks will be considered positive for illicit use if there is either a positive toxicology screen or self-reported use on that week.
|
week 4
|
|
Risky substance use
Time Frame: week 12
|
A week will be defined as having had risky substance use if it had alcohol use at risky levels ( >14 drinks/week or 4 on an occasion for men or 7/week and >3/day for women), or illicit drug use.
Weeks will be considered positive for illicit use if there is either a positive toxicology screen or self-reported use on that week.
|
week 12
|
|
Pain
Time Frame: week 4
|
The primary pain outcome will be the pain severity score form the Brief Pain Inventory
|
week 4
|
|
Pain
Time Frame: week 12
|
The primary pain outcome will be the pain severity score form the Brief Pain Inventory
|
week 12
|
|
Service Use
Time Frame: week 4
|
Service use will be coded for each week as whether the Veteran attended any pain related, substance abuse and/or mental health treatment.
Attendance at treatment during a week will be defined as having any service use data (VA or self-reported use of non-VA services) indicating use.
The difference in probability of attendance over time will be compared across treatment groups.
Use of non-VA services, and whether substance abuse was addressed during a counseling session will be self-reported.
|
week 4
|
|
Service Use
Time Frame: week 12
|
Service use will be coded for each week as whether the Veteran attended any pain related, substance abuse and/or mental health treatment.
Attendance at treatment during a week will be defined as having any service use data (VA or self-reported use of non-VA services) indicating use.
The difference in probability of attendance over time will be compared across treatment groups.
Use of non-VA services, and whether substance abuse was addressed during a counseling session will be self-reported.
|
week 12
|
Collaborators and Investigators
Sponsor
Publications and helpful links
Helpful Links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- R34AT008318-01 (U.S. NIH Grant/Contract)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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