Actively Recruiting
Magnetic Resonance Elastography to Monitor Response to Manual Therapy in Myofascial Pain
Led by Mayo Clinic · Updated on 2026-02-03
78
Participants Needed
2
Research Sites
82 weeks
Total Duration
On this page
Sponsors
M
Mayo Clinic
Lead Sponsor
N
National Center for Complementary and Integrative Health (NCCIH)
Collaborating Sponsor
AI-Summary
What this Trial Is About
The purpose of this research is to develop and test new Magnetic Resonance Imaging (MRI) methods that look at how muscles and tissues under the skin (myofascial tissues) move and respond to pressure. The investigators want to see how these tissues differ between healthy people and people with pain or injury, and how they change after hands-on treatment (Tuina therapy). The results will also be compared to a group that receives standard care without Tuina therapy. The main questions this study aims to answer are: 1. Can MR elastography (MRE) show changes in how the fascia and the layers between muscles move and stretch before and after manual therapy? 2. Do changes seen on MRE scans match changes in pain, function, and other symptoms reported by participants? 3. Can MRE measurements before treatment help predict which participants are most likely to improve with manual therapy? In this randomized controlled trial, participants with myofascial pain will be randomly assigned (randomized) to either the Tuina group or the Usual Care group following a home-based care program without manual therapy. All treatments are noninvasive, hands-on techniques commonly used in clinical practice to reduce tissue tightness and improve movement. Participants will be asked to undergo three MRI scans and to complete questionnaires and other standard clinical assessments about their pain, physical function, and quality of life.
CONDITIONS
Official Title
Magnetic Resonance Elastography to Monitor Response to Manual Therapy in Myofascial Pain
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult males or females (age 63 18 years)
- History of chronic low back pain for at least 3 months
- Presence of a palpable taut band or nodule within skeletal muscle
- Hypersensitive tender spot within the taut band
- Recognition of current pain when pressure is applied to tender nodule/taut band
- Pain limits full stretch range of motion
You will not qualify if you...
- Pregnancy or breastfeeding
- Contraindications to MRI or severe claustrophobia preventing safe scan completion
- Previous therapy in the treatment area within 3 months
- Previous severe back injury or surgery
- Neurological conditions or active systemic diseases impairing sensation or pain perception
- Severe osteoarthritis
- Skin injuries in the treatment area
- Inability to provide consent
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 2 locations
1
Mayo Clinic in Rochester
Rochester, Minnesota, United States, 55905
Enrolling by Invitation
2
Mayo Clinic Rochester
Rochester, Minnesota, United States, 55905
Actively Recruiting
Research Team
M
Melissa L Bush
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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