OMT vs. Standard Therapy in the Management of Acute Neck and Low Back Pain in the Emergency Department

St. Joseph's Regional Medical Center, New Jersey

Status

Completed

Conditions

Acute Pain

Treatments

Other: OMT vs. Ibruprofen

Study type

Interventional

Funder types

Other

Identifiers

NCT06987578

PR#19-025

Details and patient eligibility

About

Patients 18 to 65 years old who present within 72 hours of onset pain will be considered for study enrollment. Patients with the acute musculoskeletal low back or neck pain based on ED history and structural physical exam will be included. Patients will be excluded based upon specific exclusion criteria. After providing informed consent, patients will be randomized by block randomization to receive OMT or ibuprofen 400 mg, given orally.

Full description

Patients 18 to 65 years old who present withinj 72 hours of onset pain will be considered for study enrollment. Patients with acute musculoskeletal low back or neck pain based on ED history and structural physical exam will be included. Patients will be excluded based upon specific exclusion criteria. After providing informed consent, patients will be randomized by block randomization to receive OMT or ibuprofen 400 mg, given orally.

A unique patient code will be given to each patient to protect their privacy. A baseline pain score of an 11-point numeric rating scale (NRS-11) will be documented prior to the intervention. The OMT study group will receive 5 minutes of OMT treatment consisting of either or both myofascial release and muscle energy. The control group will only receive ibuprofen 400 mg in a single oral dose. At 30 and 60 minutes post intervention both groups will be asked to score their pain on the 11-point NRS scale from 0 to 10. At 60 minutes, each patient will also be asked to evaluate their perceived pain reduction on the 5-point pain reduction scale (PRS-5). A pain reduction of 50% or greater, on the NRS-11 scale, will be considered clinically significant. Additionally patients will be asked to assess whether they experienced any significant side effects, such as nausea, vomiting, epigastric pain, dizziness or worsening muscle soreness. If the patient's pain is not controlled by 60 minutes, patients will be offered rescue analgesia. The choice of analgesic will be left to the discretion of the provider, but will be recorded for analysis. Lastly, patient satisfaction and likability of treatment will be measured.

Enrollment

45 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients 18 to 65 years old who present within 72 hours of onset pain will be considered for study enrollment. Patients with acute musculoskeletal low back or neck pain based on ED history and structural physical exam will be included, provided they sign the informed consent.

Exclusion criteria

Failure to sign consent Focal neurological deficit (motor or sensory), or paresthesia
- Severe osteoporosis
- History of peptic ulcer disease
- Presentation requiring cardiac monitoring
- Fracture, dislocation, or joint instability at the area of symptoms
- Presentation after traumatic injury requiring C-collar placement prior to or subsequent to arrival
- Cancer or malignancy of the head, neck, chest or back
- Allergy to aspirin or nonsteroidal anti-inflammatory drugs
- Cellulitis (skin infection) at the treatment site
- Pregnancy or currently breastfeeding
- History of renal impairment
- Cervical or lumbar radiculopathy
- Active illicit drug abuse or chronic alcohol use
- Chronic pain syndrome
- Daily opioid use
- Use of aspirin daily
- Use of antiplatelet or anticoagulant medications (clopidogrel, warfarin, dabigatran rivaroxaban, apixaban or other similar medications)
- Glasgow Coma Scale (GCS) less than 15 or altered mental status
- Prisoners presenting in police custody
- Use of any non-steroidal antiplatelet medications (NSAIDS) or administration of any non-pharmacological manipulation (Physical Therapy or OMT) within six hours prior to presentation.