Is Conditioned Pain Modulation Predictive of Clinical Improvement in Patients With Chronic Low Back Pain?

Brooke Army Medical Center

Status: Enrolling

Conditions: Low Back Pain

Treatments: Other: Physical therapy

Study type: Interventional

Funder types: Other U.S. Federal agency

Identifiers

NCT06544525

C.2024.070

Details and patient eligibility

About

Conditioned pain modulation (CPM) a measure of the effectiveness of the descending pain pathway and therefore a measure of the body's ability to perform endogenous analgesia. In subjects with normal function of the descending pain pathway, the net-effect during CPM testing is anti-nociceptive, or inhibition of the ascending pain pathway. In those with impaired descending pain pathway function, the response to CPM testing is pro-nociceptive, indicating that the body is unable to inhibit the pain signal, or may even amplify it. There is literature that supports the presence of impaired CPM, and therefore impaired descending pain pathway function, in numerus chronic pain conditions, including low back pain. Impaired descending pain pathway function may be contributing to this chronic pain presentation. This study will give us information on whether a typical physical therapy plan of care is able to improve impaired CPM, and if CPM values are predictive of improvement in physical therapy.

Enrollment: 57 estimated patients

Sex: All

Ages: 18 to 64 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• DEERS eligible
• English speaking
• Age 18-64 years
• ODI baseline ≥25%
• NPRS baseline ≥3/10
• Low back pain symptoms greater than 3 months
• Must be able to commit to at least six weeks of physical therapy interventions

Exclusion criteria

• Serious spinal pathology (acute fracture, active cancer, inflammation, inflammatory arthropathy)
• Low back pain symptoms radiating below the knee
• Pregnancy
• Diagnosed neurological disease including traumatic brain injury, multiple sclerosis, chronic regional pain syndrome, and fibromyalgia.
• History spinal surgery
• Currently under litigation related to low back pain
• Currently going through Medical Evaluation Board (MEB)
• Retiring or separating from the military within a year

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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57 participants in 1 patient group

chronic low back pain

Experimental group

Description:

Age 18-64 years with low back pain duration greater than 3 months.

Treatment:

Other: Physical therapy