Electronic Approach to the Human Massage Therapist

Last updated: May 1, 2026
Sponsor: Mayo Clinic
Overall Status: Active - Recruiting

Phase

N/A

Condition

Chronic Pain

Lower Back Pain

Treatment

EMMA massage therapy

Clinical massage treatment

Clinical Study ID

NCT07040397
25-002863
  • Ages > 18
  • All Genders

Study Summary

The purpose of this study is to gather information about patient experience receiving a massage through a robotic EMMA (Expert Manipulative Massage Automation) compared to receiving a massage from a massage therapist.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • be 18 years of age or older.

  • report a primary pain point in the lower back.

  • Pain intensity reported at baseline

  • Women of childbearing potential who self-report not being pregnant and agree toemploy an effective method of birth control (surgical sterilization or oralcontraceptives, barrier method with spermicides, intrauterine device, etc.) duringthe study period

  • be able to participate fully in all aspects of the study.

  • have understood and signed study informed consent.

Exclusion

Exclusion Criteria:

  • Pregnancy or breastfeeding

  • Patients with the inability to stay in a prone position

  • Patients with bleeding disorders

  • Patients with allergies and/or local skin affectations

  • have used pain medications or participated in a pain treatment within three days ofstudy enrollment.

  • have an implanted device (including a lap band) in the targeted area of massagetherapy.

  • have used an investigational drug within 30 days of study enrollment.

  • have a history of any major cardiovascular events including heart valve disease,ongoing angina, cardiac arrhythmias, congestive heart failure, acute coronarysyndrome, stroke, transient ischemic attack, or peripheral vascular disease.

  • have clinically significant acute or chronic progressive or unstable neurologic,hepatic, renal, cardiovascular, lymphatic, respiratory, metabolic disease (such asuncontrolled diabetes type 2) active cancer, actively receiving treatment for canceror within 1 year of cancer remission.

  • surgical intervention for pain within 1 month prior to enrollment.

  • active infection, wound or other external trauma to the areas to be treated withmassage therapy.

  • have a known history of any condition or factor judged by the investigator topreclude participation in the study or which might hinder adherence.

Study Design

Total Participants: 40
Treatment Group(s): 2
Primary Treatment: EMMA massage therapy
Phase:
Study Start date:
January 30, 2026
Estimated Completion Date:
October 01, 2026

Study Description

Patients being evaluated in an outpatient service will be invited to participate in this study if they report a primary pain point in Low Back. Once they are enrolled in the study, they will be randomized to the type of massage therapy they will receive. Direct massage therapy through a certified massage therapist or indirect massage therapy through EMMA operated by a certified massage therapist.

Connect with a study center

  • Mayo Clinic in Rochester

    Rochester, Minnesota 55905
    United States

    Active - Recruiting

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