Joint Base Lewis Mcchord, WANCT07615816Now EnrollingIRB Ready

Lower Back Pain Clinical Trial in Joint Base Lewis Mcchord, WA

Access cutting-edge lower back pain treatment through this clinical trial at a research site in Joint Base Lewis Mcchord. Study-provided care at no cost to qualified participants.

Sponsored by The Geneva Foundation

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Expert Care in Joint Base Lewis Mcchord

Access lower back pain specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related lower back pain treatment provided free

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Check if you qualify for this lower back pain clinical trial in Joint Base Lewis Mcchord, WA

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Why Participate?

  • No-Cost Study Care

  • Local to Joint Base Lewis Mcchord

    Convenient for WA residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Joint Base Lewis Mcchord site if eligible
  4. 4Begin participation

About This Lower Back Pain Study in Joint Base Lewis Mcchord

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).

Sponsor: The Geneva Foundation

Who Can Participate

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

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Joint Base Lewis Mcchord?

Yes, this clinical trial (NCT07615816) has an active research site in Joint Base Lewis Mcchord, WA that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Lower Back Pain Treatment Options in Joint Base Lewis Mcchord, WA

If you're searching for lower back pain treatment options in Joint Base Lewis Mcchord, WA, this clinical trial (NCT07615816) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Joint Base Lewis Mcchord research site is actively enrolling participants for this clinical trial. You'll receive care from experienced lower back pain specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all lower back pain clinical trials near you to find additional studies recruiting in your area.

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