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Clinical Trials/NCT05479149
NCT05479149
Completed
Not Applicable

Effectiveness of a Novel Device for Cervical Training in Cervicogenic Headache. Randomized Clinical Trial.

Universitat Internacional de Catalunya1 site in 1 country28 target enrollmentAugust 5, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cervicogenic Headache
Sponsor
Universitat Internacional de Catalunya
Enrollment
28
Locations
1
Primary Endpoint
Change in Flexion Rotation Test (FRT)
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

The purpose of this study is to evaluate the clinical results in cervical spine range of motion, endurance deep cervical muscles, headache impact and physical activity enjoyment by a training protocol with the new device for cervical treatment (CDAT) versus conventional training protocol (CT) in subjects with cervicogenic headache.

Detailed Description

The cervical spine is the most mobile region of the spine and must be strong enough to support the weight of the skull. Strength deficits of the deep cervical muscles are related to different clinical conditions, such as cervicogenic headache. Cervicogenic headache is a secondary headache defined as a unilateral headache associated with neck pain, related to a decreased cervical range of motion and strength deficits of the deep cervical muscles. Training protocols can help to improve pain, function, posture and cross-sectional area. However, there are no training protocols in subjects with cervicogenic headache including deep neck extensor and flexor muscles. The cervical device treatment (CDAT) allows us to train the cervical flexor and extensor muscle in a simple and comfortable way.

Registry
clinicaltrials.gov
Start Date
August 5, 2022
End Date
November 15, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Pilar Pardos Aguilella

Colaborator Lecturer in Physiotherapy

Universitat Internacional de Catalunya

Eligibility Criteria

Inclusion Criteria

  • Deep flexor strength deficit in craniocervical flexion test.
  • Deep extensor strength deficit in neck extensor muscle endurance.
  • A positive result in the flexion-rotation test
  • ≥ 50 score in Headache Impact Test (HIT-6).
  • Diagnosis of cervicogenic headache according to Sjaastad et al. Subjects will have to fulfill both parts I and III of the major criteria for diagnosis (pain aggravated by neck movement, sustained position or external pressure, restricted cervical range of motion, and unilateral pain starting in the neck and radiating to the frontotemporal region)

Exclusion Criteria

  • Have received head/cervical treatment during the last six month, presented any red flag, neurological or cognitive impairment (inability to understand the questionnaires or examination).
  • Have received cervical manual therapy treatment during the last six month
  • A history of head/cervical trauma or surgery during the last year.
  • The use of pacemakers (the magnets in the CROM device could alter their signal
  • Inability to perform the flexion-rotation test.

Outcomes

Primary Outcomes

Change in Flexion Rotation Test (FRT)

Time Frame: Change between baseline and post intervention (6 weeks) and after 10 weeks.

Mean change from baseline in Flexion-rotation test after 6 weeks and 10 weeks. The examiners assess the cervical ROM using CROM (Cervical Range-of-Motion Instrument). Flexion rotation test will be evaluated. Flexion rotation test is used to see the amount of movement of the upper cervical spine and is the test most used in the literature. It is positive when there is a decrease of 10 degrees or more in the cervical rotation with maximum flexion, in a sense with respect to the contralateral or presents hypomobility of segment C1 with a mobility less than 32.

Change in Headache Impact Test (HIT-6) (Headache Disfunction)

Time Frame: Change between baseline and post intervention (6 weeks) and after 10 weeks.

Mean change from baseline in Headache Impact Test (HIT-6) after 6 weeks and 10 weeks. The examiners assess the impact of headache on patients' lives using the HIT-6. Very severe impact: 60 or more. Major impact: 56-59 score Some impact: 50-55 score Little or no impact: 49 or less.

Secondary Outcomes

  • Craniocervical flexion test(Baseline and 6 weeks, 10 weeks.)
  • Cervical Spine Range of Motion (ROM).(Baseline and 6 weeks, 10 weeks.)
  • Deep neck flexor endurance Test.(Baseline and 6 weeks, 10 weeks.)
  • Physical activity enjoyment Scale (PACES)(6 weeks)

Study Sites (1)

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