Élite Fisioterapia, María Montessori 2.
Zaragoza, 50018, Spain
NCT Number: NCT05479149
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.
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Notify Me18 year–65 year
All sexes
Interventional
Not applicable
Zaragoza, 50018, Spain
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Endurance training program of deep cervical flexors and deep cervical extensors with the cervical device for treatment.
Endurance training program of deep cervical flexors and deep cervical extensors with the conventional protocol.
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.
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.
Time frame: Baseline and 6 weeks, 10 weeks.
The examiners assess the strength of deep cervical flexors with craniocervical flexion test.
Time frame: Baseline and 6 weeks, 10 weeks.
Mean change from baseline in Cervical Spine Range of Movement (ROM) after 6 weeks and 10 weeks.
The examiners assess the cervical ROM using CROM (Cervical Range-of-Motion Instrument). Cervical flexion, extension, right/left sidebending, right/left rotation will be evaluated.
The examiners assess the cervical ROM using CROM (Cervical Range-of-Motion Instrument). Upper cervical flexion, upper cervical extension will be evaluated.[Time Frame: Baseline and 6 weeks, 10 weeks]
Time frame: Baseline and 6 weeks, 10 weeks.
Chin Tuck Neck Flexion Test is an assessment technique intended to determine the endurance of the deep cervical flexors.
Time frame: 6 weeks
The examiners assess participant satisfaction with cervical deep muscle training.
This scale measures enjoyment during physical activity through 16 items, which are preceded by the phrase "When I am active…" This instrument measures enjoyment and bipolar enjoyment, through statements such as "I enjoy it", "I'm bored", "It's very exciting", and "I don't like it". The answers will be collected on a Likert scale from 1 (totally disagree) to 5 (totally agree).
Universitat Internacional de Catalunya
Other
Effectiveness of a Novel Device for Cervical Training in Cervicogenic Headache. Randomized Clinical Trial.
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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