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COMPARISON OF THE EFFECTIVENESS OF CERVICAL TRANSLATORIC MOBILIZATIONS WITH CERVICAL STABILITY TRAINING IN FEMALE PATIENTS WITH CERVICOGENIC HEADACHE: A RANDOMIZED CONTROLLED TRIAL

Comparison of the effectiveness of Cervical Translatoric Mobilizations with Cervical Stability Training in female patients with Cervicogenic Headache

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220518054910N1
Enrollment
82
Registered
2023-05-31
Start date
2023-03-15
Completion date
Unknown
Last updated
2023-06-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cervicogenic Headache. Other headache syndromes

Interventions

Intervention 1: Intervention group: Cervical Translatoric Mobilizations. Intervention 2: Intervention group: Cervical Stability Training.

Sponsors

King Edward Medical University, Mayo Hospital Lahore
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: The study will include female patients aged 20-40 years. A diagnosis of cervicogenic headache (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) Positive cervical flexion-rotation test (FRT)

Exclusion criteria

Exclusion criteria: Patients previously receiving treatment for underlying pathology. Patients presented with red flag signs for headache. Patients presented with migraine. Patients in whom manual therapy is contraindicated. Patients who are diagnosed with radiculopathy. Patients who are taking analgesics.

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Before applying Intervention and at week 3 and week 6 of intervention. Method of measurement: Visual Analogue Scale.;Range of Motion (Upper Cervical). Timepoint: Before applying Intervention and at week 3 and week 6 of intervention. Method of measurement: Goniometer.;Range of Motion (General Cervical). Timepoint: Before applying Intervention and at week 3 and week 6 of intervention. Method of measurement: Goniometer.

Countries

Pakistan

Contacts

Public ContactYasham Afzal

King Edward Medical University, Mayo Hospital Lahore

yashamafzal61@gmail.com+92 323 7888180

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026