Sacramento, CANCT07494162Now EnrollingIRB Ready

Myofascial Pain Syndrome (MPS) Clinical Trial in Sacramento, CA

Access cutting-edge myofascial pain syndrome (mps) treatment through this clinical trial at a research site in Sacramento. Study-provided care at no cost to qualified participants.

Sponsored by University of California, Davis

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Expert Care in Sacramento

Access myofascial pain syndrome (mps) specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related myofascial pain syndrome (mps) treatment provided free

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Check if you qualify for this myofascial pain syndrome (mps) clinical trial in Sacramento, CA

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Sacramento

    Convenient for CA 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 Sacramento site if eligible
  4. 4Begin participation

About This Myofascial Pain Syndrome (MPS) Study in Sacramento

This study will evaluate the clinical and biological effects of acupuncture for chronic low back pain associated with myofascial pain syndrome (MPS). In this randomized, participant- and assessor-blinded clinical trial, 64 adults with chronic low back pain due to MPS will be assigned to receive either true acupuncture or sham acupuncture for eight weeks. Participants will undergo total-body positron emission tomography/computed tomography (TB-PET/CT) imaging and complete standardized pain and functional questionnaires at baseline and after treatment. The study will evaluate whether acupuncture improves pain and function compared with sham treatment and whether TB-PET/CT imaging can detect changes in myofascial tissue metabolism and perfusion that correspond with clinical outcomes.

Sponsor: University of California, Davis

Who Can Participate

Inclusion Criteria

Ability to understand the purposes and risks of the trial and willingness to sign an informed consent form
Willingness and ability to comply with all protocol required procedures
Willingness to be randomized to receive either true acupuncture or sham acupuncture
Current self-report of chronic low back pain (cLBP) which has persisted for the past 3 months AND has resulted in pain on \> 50% of days in the past 6 months
At least one palpable nodule or taut band in paraspinal, quadratus lumborum, or gluteal muscles
Reproduction of the patient's dominant pain with palpation of a muscle nodule or taut band
Predominantly paramedian pain (may be uni-lateral or bi-lateral)
Willing and able to lay motionless in a supine position at least twice, preferably thrice: 70-minute TB-PET/CT scan
Willing and able to fast for at least 6 hours before and for the duration of the TB-PET/CT scan
Willing to avoid strenuous exercise for 24 hours before the TB-PET/CT scan visit
Willingness to practice effective contraception during the study.

Exclusion Criteria

No Primary Care Physician
History of spine infection (discitis or osteomyelitis) or spine tumor
History of ankylosing spondylitis, rheumatoid arthritis, polymyalgia rheumatica, psoriatic arthritis, or lupus
Confounding conditions that are known to be responsible for inducing pain
Implants at or in the region of the sites of interest
Diagnosis of any vertebral fracture in the last 6 months
Cauda equina syndrome or lumbar radiculopathy with functional motor deficit (strength\<4/5 on manual motor testing)
Spinal implants (including fixation hardware, spinal cord stimulator, intra-thecal pumps, that are present in the region of the sites of interest)
Predominantly central pain
Pain below the knee
Positive straight leg raise test
Symptomatic hip arthritis
Uncontrolled claustrophobia
Pregnant or lactating participants
Body weight more than 225 kg (496 pounds) due to the weight limitation of the scanner bed
Inability to speak, read, and write in the English language
Concurrent or prior enrollment in a separate research study involving a PET scan performed within the last 12 months for research purposes only. That is, PET scans are not performed as part of a patient's treatment plan (e.g. standard of care, therapeutic purposes, or clinical care) and the research study did not intend to provide therapeutic benefit to the patient. •Any other criteria, which would make the participant unsuitable to participate in this study as determined by the Principal Investigator

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 Sacramento?

Yes, this clinical trial (NCT07494162) has an active research site in Sacramento, CA 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.

Myofascial Pain Syndrome (MPS) Treatment Options in Sacramento, CA

If you're searching for myofascial pain syndrome (mps) treatment options in Sacramento, CA, this clinical trial (NCT07494162) 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 Sacramento research site is actively enrolling participants for this clinical trial. You'll receive care from experienced myofascial pain syndrome (mps) 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 myofascial pain syndrome (mps) clinical trials near you to find additional studies recruiting in your area.

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