Evaluation of a Peer Coach-Led Intervention to Improve Pain Symptoms
| Status: | Active, not recruiting |
|---|---|
| Conditions: | Chronic Pain, Chronic Pain, Pain |
| Therapuetic Areas: | Musculoskeletal |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 12/23/2018 |
| Start Date: | May 1, 2015 |
| End Date: | June 30, 2019 |
Evaluation of a Peer Coach-Led Intervention to Improve Pain Symptoms (ECLIPSE)
To maximize implementation potential of pain self-management in the VA, alternative delivery
methods are needed to provide Veterans with education and support needed to self-manage their
pain, without requiring additional resources from healthcare teams. A novel and promising
approach is a peer coaching model, in which Veterans with chronic pain who are successfully
managing their pain offer information, support, and mentorship to other Veterans with pain.
methods are needed to provide Veterans with education and support needed to self-manage their
pain, without requiring additional resources from healthcare teams. A novel and promising
approach is a peer coaching model, in which Veterans with chronic pain who are successfully
managing their pain offer information, support, and mentorship to other Veterans with pain.
The investigators' goal is to test the effectiveness of a peer coaching model among Veterans.
The investigators are examining feasibility for implementation alongside effectiveness, to
shorten the timeline to implementation.
Aim 1 (primary aim): To compare 6-month (primary endpoint) and 9-month (sustained effects)
effects of peer-supported chronic pain self-management versus controls on overall pain
(intensity and function).
Hypothesis 1: Veterans in the peer support arm will experience reduced overall pain compared
to controls.
Aim 2 (secondary aim): To compare 6- and 9-month effects of peer-supported chronic pain
self-management versus controls on self-efficacy, social support, pain coping, patient
activation, health-related quality of life, and health service utilization.
Hypothesis 2: Veterans in the peer support arm will experience greater self-efficacy, social
support, pain coping, patient activation, and health-related quality of life, and lower
health service utilization, compared to controls.
Aim 3 (pre-implementation aim): To explore facilitators and barriers to implementation of
peer support for chronic pain, intervention costs, and fidelity to the model.
The investigators are examining feasibility for implementation alongside effectiveness, to
shorten the timeline to implementation.
Aim 1 (primary aim): To compare 6-month (primary endpoint) and 9-month (sustained effects)
effects of peer-supported chronic pain self-management versus controls on overall pain
(intensity and function).
Hypothesis 1: Veterans in the peer support arm will experience reduced overall pain compared
to controls.
Aim 2 (secondary aim): To compare 6- and 9-month effects of peer-supported chronic pain
self-management versus controls on self-efficacy, social support, pain coping, patient
activation, health-related quality of life, and health service utilization.
Hypothesis 2: Veterans in the peer support arm will experience greater self-efficacy, social
support, pain coping, patient activation, and health-related quality of life, and lower
health service utilization, compared to controls.
Aim 3 (pre-implementation aim): To explore facilitators and barriers to implementation of
peer support for chronic pain, intervention costs, and fidelity to the model.
Inclusion Criteria:
- have musculoskeletal pain in the low back, cervical spine, or extremities (hip, knee,
or shoulder) for 3 months
- have at least moderate pain severity, defined by pain 5 on a 0 (no pain) to 10 (worst
pain imaginable) scale
- indicate willingness to engage in phone or in-person contact on a regular basis with
another Veteran
Exclusion Criteria:
- if the electronic medical record indicates a diagnosis of a psychotic disorder (e.g.,
International Classification of Diseases (ICD) ICD-9 codes 295-295.9 for
schizophrenia)
- current substance dependence (e.g., ICD-9 codes 304-304.9)
- severe medical conditions precluding participation (e.g., New York Heart Association
Class III or IV heart failure, ICD-9 codes 428-428.9 )
- if the eligibility screener given to prospective participants reveals active suicidal
ideation severe hearing or speech impairment
- pending surgery for a musculoskeletal condition (e.g., back surgery)
We found this trial at
1
site
Indianapolis, Indiana 46202
Phone: (317) 988-2722
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