Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07278570

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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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

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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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