A Study Of Magnetic Resonance Elastography Of Myofasial Pain

Overview

About this study

The purpose of this study is to evaluate the ability of MRE-derived fascia mechanical properties to monitor treatment response to physical force-based manual therapies and predict patient outcomes.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Adult males or females (age ≥ 18 years)

  • A history of chronic low back for at least 3 months. (Measured by patient history and physical exam)

  • A palpable taut band or nodule within the skeletal muscle

  • Hypersensitive tender spot within the taut band

  • Recognition of current pain complaint by pressure on the tender nodule/taut band

  • Painful limit to the full stretch range of motion

 

Exclusion Criteria:

  • Pregnancy or breastfeeding

  • Any contraindication to an MRI exam, or severe claustrophobia that would prevent safe completion of the scan

  • Previous therapy in the area to be treated within 3 months

  • Previous severe back injury (including fracture) or surgery

  • Any neurological conditions or active systemic disease (e.g. diabetes, peripheral vascular disease, cancer, rheumatoid arthritis) that impaired sensation/pain perception

  • Severe osteoarthritis

  • Skin injuries in the area to be treated

  • Known or suspected clinically significant lumbar disc or other structural spinal pathology considered to be the primary cause of the participant’s symptoms or makes study participation or manual therapy inappropriate.

  • Have a known history of any condition or factor judged by the investigators to preclude participation in the study or which might hinder adherence

  • Inability to provide consent

Note: Other protocol defined Inclusion/Exclusion Criteria may apply.

Eligibility last updated 08/04/2026. Questions regarding updates should be directed to the study team contact.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

Ziying Yin, Ph.D.

Open for enrollment

Contact information:

Paul Lewis

5072841171

lewis.paul2@mayo.edu

More information

Publications

Publications are currently not available