Recruiting

Brief ReliefMindfulness Intervention for Chronic Musculoskeletal Pain Relief

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What is being tested

Brief Mindfulness Oriented Recovery Enhancement

+ Empowered Relief

+ Mindfulness Oriented Recovery Enhancement

Behavioral
Who is being recruted

Neurologic Manifestations+2

+ Pain

+ Signs and Symptoms

Over 18 Years
See all eligibility criteria
How is the trial designed

Treatment Study

Interventional
Study Start: August 2025
See protocol details

Summary

Principal SponsorFlorida State University
Study ContactAdam Hanley, PhD
Last updated: December 11, 2025
Sourced from a government-validated database.Claim as a partner

Study start date: August 14, 2025

Actual date on which the first participant was enrolled.

The study conducted by researchers at Florida State University focuses on finding the optimal treatment duration for people suffering from chronic musculoskeletal pain. This condition includes long-term pain affecting muscles, bones, and joints. The study aims to determine how different lengths of pain management training can help reduce pain effectively. By comparing two brief training sessions against a standard-length training session, the researchers hope to identify the best approach that provides significant pain relief while being time-efficient for patients. This research is important as it could lead to more effective and accessible pain management strategies for those dealing with chronic pain. Participants in this study will be randomly assigned to one of three groups. Two groups will participate in a brief, single 2-hour online session, while the third group will attend eight weekly 2-hour online sessions. In all sessions, a trained facilitator will teach pain management techniques that have been proven to be effective through research. Participants will also complete short surveys at various stages: before starting the treatment, right after the session, and over several weeks afterward, to track their pain levels and the effectiveness of the training. This design helps researchers understand not only how well the techniques work immediately but also their lasting impact over time.

Official TitleBrief MORE: A Mindfulness Intervention For Chronic Musculoskeletal Pain 
NCT07193095
Principal SponsorFlorida State University
Study ContactAdam Hanley, PhD
Last updated: December 11, 2025
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

39 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Neurologic ManifestationsPainSigns and SymptomsPathological Conditions, Signs and SymptomsChronic Pain

Criteria

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.

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

3 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

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

Group II

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

Group III

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

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Recruiting

Research Building B

Tallahassee, United StatesSee the location
Recruiting
One Study Center