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Cranial Osteopathic Manipulative Medicine as an Adjunct Treatment for Concussion

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Northwell Health

Status

Completed

Conditions

Concussion Injury of Cerebrum
Cranial Osteopathic Medicine

Treatments

Other: Cranial Osteopathic Manipulative Medicine

Study type

Interventional

Funder types

Other

Identifiers

NCT03225599
Concussion COMM

Details and patient eligibility

About

Patients who have concussions exhibit an array of symptoms, also known as post-concussive symptoms, including headaches, feeling slowed down or foggy and difficulty with concentration. This study aims to determine if cranial osteopathy can provide additional or expedited symptom relief when accompanying current conventional treatments. The patients will be identified through routine clinical contact. If patients are found to be eligible and agree to participate, they receive a single session of cranial osteopathy in addition to their usual care through the concussion program.

Enrollment

9 patients

Sex

All

Ages

14+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Concussion occurred within 8 weeks
  • Age greater or equal to 14 years
  • Complains of post-concussive symptoms with a symptom score of >10 on PCSS

Exclusion criteria

  • Concussion occurred > 8 weeks
  • Age less than 14 years
  • Surgery of the cervical and/or thoracic spine within the last 3 months
  • Currently receiving or has received workers compensation within the last 3 months
  • Currently or potentially become involved in litigation related to the injury
  • Received osteopathic craniosacral treatments within the last 3 months
  • History of hydrocephalus, current infection or active tumor
  • Active or marked depression, anxiety or psychosis

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

9 participants in 1 patient group

Procedure
Experimental group
Treatment:
Other: Cranial Osteopathic Manipulative Medicine

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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