Medical Massage Therapy for Subacute Lower Back Pain in Active-Duty Service Members
Official title: Investigating Medical Massage Therapy for Patients With Sub-Acute Lower Back Pain
Run by The Geneva Foundation · NCT07615816 · Data updated 2026-11-12
This study tests whether adding medical massage therapy to standard care can shorten duty-restriction periods and reduce pain for active-duty service members with subacute lower back pain.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 64 Years |
| Sex | All |
| Enrollment | 220 (estimated) |
| Sponsor | The Geneva Foundation Academic / other |
| Locations | 1 site (Joint Base Lewis McChord, Washington) |
| Status | Recruiting |
| Started | June 1, 2026 |
| Main results expected | January 31, 2027 |
| Study ends | January 31, 2027 |
| Registry record updated | June 5, 2026 |
| Trial ID | NCT07615816 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Active-duty service members aged 18-64 with subacute low back pain (1–3 months) willing to participate and comply with treatment and follow-up.
✕Probably not a fit
Individuals with certain exclusion criteria such as significant comorbid pain, active infections, or serious autoimmune conditions may not benefit or be eligible for the study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
Participants are active-duty service members aged 18-64 with subacute low back pain lasting 1-3 months. The trial randomizes them to receive provider-directed care alone or provider-directed care plus a weekly medical massage therapy session over about 12 weeks. The study looks at duration of medically restricted duty days, pain levels, and healthcare utilization to see if the massage addition provides additional benefit beyond standard care. It uses a two-group design to compare outcomes between the intervention and control arms, with follow-up aligned to the 12-week period (+/- 2 weeks). The Geneva Foundation leads the trial with collaboration from Uniformed Services University and Madigan Army Medical Center at Madigan Army Medical Center, Joint Base Lewis-McChord.
Why it matters
Potential benefit: If successful, participants receiving massage therapy may experience shorter duty restrictions and better pain management, potentially reducing healthcare utilization.
How similar studies have gone: Previous research on massage therapy for low back pain shows promise, but there have been few large randomized trials in subacute, active-duty populations; this study aims to add rigorous evidence in that context.
Who can join: the full rules
Show full inclusion / exclusion 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
Where it's running
-
Madigan Army Medical Center
Joint Base Lewis McChord, Washington, United States Recruiting
Study contacts
- Principal investigator: Ghena G. Grinshpun, PhD, MBA, MSF, PMP — Madigan Army Medical Center
- Study coordinator: Janel Son, MPH
- Email: json@genevausa.org
- Phone: 253-968-3288
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.