Comparison of the Eficacy of Mulligan Mobilization and Myofascial Release in Patients With Cervicogenic Headache
1 other identifier
interventional
90
1 country
1
Brief Summary
Cervicogenic headache (CBH) is defined as a headache caused by a disorder in the cervical spine, bones, discs, or soft tissue elements, which is also accompanied by neck pain. Unilateral, non-reversible oculo, fronto, temporal pain, pain that increases with poor neck positioning and incorrect neck movements, and may be seen with restricted movement in the upper cervical and occiput regions. The aim of this thesis is to compare the effectiveness of Mulligan mobilization technique and myofascial release methods used in the treatment of cervicogenic headache through a prospective clinical study.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Dec 2025
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
December 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2025
CompletedFirst Submitted
Initial submission to the registry
December 25, 2025
CompletedFirst Posted
Study publicly available on registry
April 2, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2026
ExpectedApril 2, 2026
March 1, 2026
Same day
December 25, 2025
March 30, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Frequency of cervicogenic headache
To determine the frequency of cervicogenic headaches, patients were given a headache diary.
Beginning, week 4, and week 8
assessment of pain intensity VAS pain (0-10)
0 no pain, 10 unbearable/maximum pain
Beginning, week 4, and week 8
Secondary Outcomes (3)
Headache impact scale (HIT)
Beginning, week 4, and week 8
Headache disability inventory/indexi ( HDI )
Beginning, week 4, and week 8
Assessment of quality of life short form-12
Beginning, week 4, and week 8
Study Arms (3)
Mulligan mobilization technique
EXPERIMENTALIn addition to mulligan mobilization therapy, which will be given three times a week for four weeks (12 sessions in total), a home exercise program will be provided.
Myofascial release therapy
EXPERIMENTALIn addition to myofascial release therapy, which will be given three times a week for four weeks (12 sessions in total), a home exercise program will be provided.
A home workout program
ACTIVE COMPARATORA home workout program will be provided three times a week for four weeks (12 sessions in total).
Interventions
Each patient was asked to sit comfortably, and the therapist performing the treatment stood beside them. The patient's head was free and positioned between the therapist's right forearm and body, with the therapist standing to the patient's right. The therapist then placed their right index, middle, and ring fingers on the base of the occiput and held their right little finger on the spinous process of C2. Next, gentle pressure was applied ventrally and upward (45 degrees) to the lateral edge of the left thenar process and the right little finger. The gliding motion was applied rhythmically (three times per second) ten times. The therapist continuously slid the joint and actively asked the patient to move their head towards the side where the dysfunction and pain were located. He held the SNAG technique for 10 seconds. This technique was repeated 10 times over approximately 8 minutes.
The procedure was performed on the upper part of the trapezius muscle and the levator scapulae muscle. The patient was in a seated position, hips higher than knees, feet slightly in front of the knees and in full contact with the ground. The therapist stood behind the patient. Myofascial release of the trapezius was performed unilaterally with a soft fist, while the patient lowered their head forward and slowly rotated, creating a tension line from the middle of the trapezius towards the acromion process. During this time, the patient was asked to turn their head to the opposite side. Then, the therapist applied resistance to the opposite side of the rotation for 10 seconds. MGT was repeated 5 times on the trapezius. The therapist applied the same unilateral contraction, but the tension line was slightly laterally towards the lower edge of the scapula. The therapist then asked the patient to tilt their head forward to increase resistance on the levator scapula for 10 seconds.
All patients were given a home exercise program consisting of neck joint range of motion exercises, trapezius stretches, and isometric strengthening exercises for the neck muscles. The home exercise program was initiated with 3 sets of 10 repetitions per day. The exercises were demonstrated practically by the physician, and all patients were given a printed sheet showing how to perform the exercises. Patients were contacted by phone once a week to inquire about their adherence to the exercise program and were encouraged to follow it. Patients with exercise adherence below 75-80% were excluded from the study.
Eligibility Criteria
You may qualify if:
- Individuals aged 18-65
- Having experienced neck or headache for 3 months
- Meeting the diagnostic criteria for cervicogenic headache;
- Unilateral pain
- Reduced range of motion in the neck
- Ipsilateral shoulder discomfort
- Ipsilateral arm discomfort
- Pain that worsens with different neck movements and is painful on palpation
You may not qualify if:
- Migraine
- Cluster headache
- Cervical radiculopathy
- Entrapment neuropathy
- Myelopathy
- Rheumatoid arthritis
- Undergoing cervical spinal surgery
- Pregnant women
- Those who received physical therapy within 6 months
- Those with a history of major psychiatric illness
- Those with a history of uncontrolled systemic diseases (cardiovascular, pulmonary, hepatic, renal, hematological)
- Those with a history of uncontrolled systemic endocrine diseases (dm, hyperthyroidism)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Konya Beyhekim Eğitim ve Araştırma Hastanesi
Konya, 42060, Turkey (Türkiye)
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER GOV
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 25, 2025
First Posted
April 2, 2026
Study Start
December 1, 2025
Primary Completion
December 1, 2025
Study Completion (Estimated)
December 1, 2026
Last Updated
April 2, 2026
Record last verified: 2026-03