IMproving Pain Using Peer RE-inforced Self-management Skills

Not Applicable

Completed

Conditions: Chronic Pain

Interventions: Behavioral: Peer-Delivered Pain Self-Management

Registration Number: NCT01748227

Lead Sponsor: US Department of Veterans Affairs

Brief Summary: The overall purpose of this pilot study is to conduct a formative evaluation of (veteran)peer delivery of a chronic pain self-management program to veterans with chronic musculoskeletal pain.

Our specific aims are as follows:

Aim 1: Evaluate the feasibility of identifying, recruiting, training, and retaining veteran peers to implement a self-management program for chronic pain.

Aim 2: Identify facilitators and barriers to peer-delivery of a chronic pain self-management program.

Aim 3: Convene an expert panel to review the results of Aims 1 and 2, help to interpret the results, and plan next steps.

Detailed Description: This is a one-arm pilot study with a pretest/posttest design. Thus, participants' (n=20) baseline scores were compared to their final outcome assessment scores (i.e., change scores.) There was no control group.

This study is an intervention using peer coaches to deliver pain self-management instruction to patients. Peer coaches thus delivered the intervention and underwent a 3-hour training session prior to initiation of the study. Because peers served as intervention facilitators and not as recipients of the intervention, this study was not focused on peer outcomes.

Patients (n=20) attended a 2-hour didactic session led by the study nurse. Then patients were assigned a peer (2 patients per peer). Patients met with their peers for 4 months to discuss pain self-management with the guidance of a study manual. Peers were asked to contact patients a minimum of bi-weekly via telephone or in-person.

Peers reviewed each of the topic areas covered in the self-management manual. Peers reviewed a different topic each session, ask if the patient has questions, and discuss his or her personal experience with the topic being covered during that session. Modeling what the nurse care manager has done in prior studies, peers worked with patients to help them to set goals and to evaluate whether these goals are realistic. A new goal was set at each session, with the peer following up on the previous goals with the patient, whether they were accomplished, and if not, possible courses of action (e.g., modifying the goal or offering other advice to accomplish the goal). Throughout these sessions peers were encouraged to draw on their own experiences and how they personally overcame obstacles and handled setbacks and frustrations. Peers did not advise on or discuss medications or medical questions with patients.

Participating patients (n=20) were given outcome assessments at baseline and at 4-month follow-up.

Recruitment & Eligibility

Status: COMPLETED

Sex: All

Target Recruitment: 20

Inclusion Criteria

Peers will be eligible if they have chronic musculoskeletal pain and have completed a pain self-management program from any of these chronic pain trials:
- Stepped Care for Depression and Musculoskeletal Pain (SCAMP)
- Evaluation of Stepped Care for Chronic Pain in Iraq and Afghanistan Veterans (ESCAPE)
- CAre Management for the Effective use of Opioids (CAMEO)
- Or participants of the VA Pain School or VA Pain program
- Peers may also be recommended by their primary care providers at the VA
Eligible patients must have musculoskeletal pain in the low back, cervical spine, or extremities (hip, knee, or shoulder) that has persisted for 3 months
And have pain of at least moderate intensity as defined by a Brief Pain Inventory score 5

Exclusion Criteria

Patients will be excluded if they have active suicidal ideation
Have been hospitalized for psychiatric or substance abuse reasons in the last 6 months pending back surgery
Current substance dependence
Severe medical conditions (e.g., New York Heart Association Class III or IV heart failure) that precludes participation
Or severe hearing or speech impairment

Study & Design

Study Type: INTERVENTIONAL

Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Peer-Coached Pain Self-Management	Peer-Delivered Pain Self-Management	Participants (n=20) were assigned to a peer coach, who delivered self-management instruction one-on-one over a 4-month period.

Primary Outcome Measures

Name	Time	Method
Pain/Enjoyment of Life/General Activity	Change from baseline to 4 month assessment	3-item version of the Brief Pain Inventory. Possible range: 0-30. 0=no pain/interference, 30=maximum pain/interference. Thus lower values represent a better outcome.

Secondary Outcome Measures

Name	Time	Method
Pain Catastrophizing Scale	Baseline and 4 month assessment (final assessment)	Pain Catastrophizing Scale. 13-item scale. Possible score range 0-52, with lower scores representing improvement.
Multidimensional Perceived Social Support Scale (MPSS).	Baseline and 4 month for Statistical Package for Social Scientists (SPSS) and only 4 month final interview for Working Alliance	12 items, possible range 12-84 with higher scores indicating higher social support (i.e., better outcomes).
Patient Reported Outcome Measurement System (PROMIS)	Change from baseline to 4 month assessment	Possible scores range 0-100. Higher scores represent higher pain interference. Thus lower scores represent better outcomes.
Pain Centrality Scale	4 month assessment	Possible range 10-50. Higher scores indicate higher pain centrality, i.e., worse outcomes.