This Project is a Three-arm RCT Evaluating Two, Single-session Behavioral Interventions for Adults With Chronic Musculoskeletal Pain (CMP) -- 1) Brief Mindfulness-Oriented Recovery Enhancement (B-MORE) vs. Empowered Relief (ER) -- Relative to the Traditional 8-week Version of MORE. (Brief Relief)

Florida State University

Status: Enrolling

Conditions: Chronic Musculoskeletal Pain

Treatments: Behavioral: Brief Mindfulness Oriented Recovery Enhancement; Behavioral: Mindfulness Oriented Recovery Enhancement; Behavioral: Empowered Relief

Study type: Interventional

Funder types: Other

Identifiers

NCT07193095

00006036

Details and patient eligibility

About

Researchers at Florida State University are investigating how the length of treatment influences outcomes for individuals with chronic musculoskeletal pain. The goal is to identify the most effective balance between treatment duration and pain relief. There are three treatment conditions in this study: two different brief pain management trainings and one standard-length training. Participants will be randomized to either of the brief trainings, attending a single, 2-hour, online training session, in which a trained facilitator will teach pain management techniques that are backed by research. If randomized to receive the standard-length training, participants will attend eight, 2-hour, online training session over eight weeks, in which a trained facilitator will also teach research-backed pain management techniques. Short surveys will be required at seven different time points: before starting treatment, immediately after the pain-management training, and then 2, 6, 12, 24, and 36 weeks after the training.

Enrollment: 39 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• (1) having a chronic musculoskeletal pain condition, (2) average pain of ≥ 3 in the previous week, (3) willingness to engage with study assessments and interventions, (4) understanding English instructions fluently, and (5) being 18 and above.

Exclusion criteria

• (1) unable to consent because of physical or mental incapacity, (2) have previous, formal mindfulness training (e.g., MBSR) or previously receiving Empowered Relief, (3) have pain from a current cancer diagnosis or cancer-related treatment, (4) unstable illness that may interfere with treatment, (5) had surgery within the previous three months, and (6) had pain relieving injections, such as cortisone or hyaluronate, within the previous three months.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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39 participants in 3 patient groups

Brief Mindfulness Oriented Recovery Enhancement (B-MORE)

Experimental group

Description:

B-MORE is a 2-hour, single session adaptation of the traditional MORE program.

Treatment:

Behavioral: Brief Mindfulness Oriented Recovery Enhancement

Empowered Relief (ER)

Experimental group

Description:

ER is an evidence-based 2-hour single session intervention for chronic pain

Treatment:

Behavioral: Empowered Relief

Mindfulness Oriented Recovery Enhancement (MORE)

Experimental group

Description:

MORE is an 8-week evidence-based treatment for chronic pain.

Treatment:

Behavioral: Mindfulness Oriented Recovery Enhancement