Modifications in patients with subacute or chronic mechanical neck pain after osteopathic treatment and conventional physiotherapeutic treatment

Not Applicable

Recruiting

• Conditions: Patients with cervical pain.; Patients with cranial-mandibular pain.; Pacients diagnosed with subacute or chronic mechanical cervical pain; Musculoskeletal - Other muscular and skeletal disorders; Physical Medicine / Rehabilitation - Physiotherapy; Injuries and Accidents - Other injuries and accidents; Physical Medicine / Rehabilitation - Other physical medicine / rehabilitation; Alternative and Complementary Medicine - Other alternative and complementary medicine; Musculoskeletal - Normal musculoskeletal and cartilage development and function

• Registration Number: ACTRN12619001137189
• Lead Sponsor: Fisioclinic Physioteraphy private Clinic

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2019-08-14
• Last Update Posted: 5 January 2021

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

Patients with symptoms of cervical pain, diagnosed with subacute or chronic mechanical neck pain. Chronic mechanical neck pain (CMC)
-Patients with limitation in the opening of the mouth of less than 40mm, without the need to suffer symptoms in the ATM
-Whole age (between 18 and 50 years old)
-With signed written consent.
-No difference of sex.
-Patients dysfunction or disorders in the high cervical

Exclusion Criteria

- Any surgical intervention in upper limbs, head or spine at any time of their lives.
- Having received previous osteopathic treatment in the last two months.
- Having received medical treatment two weeks before the study.
- Refusal of the patient to participate in the study.
- Any Contraindication to the application of the treatment or evaluations.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Mouth opening assessed using a caliber scientifically validated, [7 days (primary timepoint) and 15 days after intervention commencement <br>];Composite primary outcome: masseter and temporal triggerspoint pain thershold assessed using a scientifically validated algometer.[7 days (primary timepoint) and 15 days after intervention commencement];cervical mobility assessed using a scientifically validated goniometer[7 days (primary timepoint) and 15 days after intervetion commencement]

Secondary Outcome Measures

Name	Time	Method
Cervical pain as assessed by Neck Disability Index[15 days post commencement of intervention]