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Investigating Medical Massage Therapy for Patients With Sub-Acute Lower Back Pain

Recruiting

Who can join

Ages 18 to 64 · All sexes

Full eligibility criteria
Inclusion Criteria:

* Active-duty service member
* 18-64 (inclusive) years of age
* Medical evidence of subacute low back pain (as indicated by complications lasting 1-3 months)
* Willingness to comply with treatment and follow-up schedule
* Ability and willingness to provide written informed consent

Exclusion Criteria:

* Current dx of any of the following:
* Presence of significant comorbid pain (e.g., polytrauma)
* Cancer - active/ongoing treatment for
* Active Infections, including skin lesions and rashes
* Flu or other severe cold virus or COVID
* Severe depression or anxiety
* Symptomatic Inflammatory/Autoimmune diseases such as Rheumatoid
* Arthritis and Ankylosing Spondylitis. Acute exacerbation and not in remission
* High Grade Spondylolisthesis (Grade III and Grade IV)
* Fibromyalgia
* Severe Osteoporosis (BMD with T-score of -2.5 or lower, along with the presence of one or more fragility fractures)
* Neurogenic conditions
* Spinal Stenosis with active neurogenic claudication
* Cauda Equina Syndrome - acute
* Radiating pain below the knee or in the presence of true Neurological signs (numbness/weakness)
* Historical dx of any of the following:
* Spinal Cord injuries with persisting neurogenic sensory or motor loss
* Lumbar spine back surgery within the past year
* Received spinal interventions (e.g., surgery, nerve ablations, steroid injections, etc.) within the past 6 months
* Current use of blood thinners/anticoagulants
* Is enrolled or plans to enroll in another clinical trial during this study that would affect the patient's safety or results of this trial
* \[Females only\] Currently pregnant (self-reported) or plans to become pregnant during the study intervention period

About the study

The goal of this clinical trial is to determine if a weekly regimen of Medical Massage Therapy (MMT) with provider-directed care shortens the duration of Medically Restricted Duty Days (MRDD) periods in Active-Duty Service Members with Subacute Lower Back Pain (LBP) compared to provider-directed care alone.

The main question the study aims to answer is, when used as an adjunct to provider-directed care, a consistent program of MMT provided by a qualified practitioner, will shorten the duration of MRDD periods, reduce pain, and decrease unnecessary healthcare utilization in patients with Subacute LBP compared to provider-directed care alone. Researchers will study this hypothesis through the comparison of Group #1 (provider-directed care alone) and Group #2 (provider-directed care and MMT).

Participants randomized into the two study groups will be following a 12-week study design (+/- 2 weeks) comprised of their compliance to their provider-directed care, the study intervention (if randomized to Group #2) and study case report forms (CRFs); with a final follow up visit (up to 4 weeks following their final treatment visit).

What is being tested

Sponsor: The Geneva Foundation · Participants: 220 · Started: Jun 1, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07615816

Locations in the U.S.

WashingtonMadigan Army Medical Center, Joint Base Lewis McChord

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.