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Myofascial Pain and Central Sensitization

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University of Michigan

Status

Completed

Conditions

Myofascial Pain
Physical Therapy

Treatments

Other: Physical Therapy

Study type

Observational

Funder types

Other

Identifiers

NCT04929171
HUM00093722

Details and patient eligibility

About

This prospective, observational cohort pilot study compared pain phenotyping and functional measures in 30 participants with non-acute neck and/or shoulder girdle pain consistent with primary myofascial pain at 3-months following a physical therapy referral to study the impact of their baseline degree of pain amplification.

Enrollment

30 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • English-speaking participants
  • Diagnosed by their physician with non-acute (more than two weeks) neck and/or shoulder girdle primary myofascial pain
  • Referred to a physical therapy treatment.

Exclusion criteria

  • In an effort to reduce the potential that another medical condition could lead to a secondary myofascial pain response, extensive comorbid exclusion criterion.
  • Use of chronic high-dose opioid medication greater than 100 mg oral morphine equivalents per day.
  • Individuals receiving or applying for compensation or disability.
  • The inability to provide informed consent.
  • Severe physical impairment (e.g., blindness, deafness)
  • Co-morbid medical condition limiting function (e.g., malignant cancer)
  • Reported illicit drug use
  • Severe psychiatric condition that would limit judgment.
  • Lack of internet access.

Trial design

30 participants in 1 patient group

Patients with myofascial pain having centralized pain features
Description:
Adult patients with myofascial pain having centralized pain features who will be undergoing physical therapy
Treatment:
Other: Physical Therapy

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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