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Study identifier: NCT06875869 Synced from ClinicalTrials.gov · July 28, 2026
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Ischemic Compression Technique Versus Jones Technique in Cervicogenic Headache Patients

Condition: Cervicogenic Headache  ·  Sponsor: Riphah International University

PhaseNA
Planned participants32
Who can joinAll sexes, 25 Years to 35 Years
Healthy volunteersNo

About this study

The primary objective of the study is to determine the effects of Jones and Ischemic compression technique on pain, range of motion and disability in patients with cervicogenic headache. Cervicogenic headache is a distinctive type of secondary headache where the pain originates from structures in the neck or cervical spine and radiates to the head. Trigger point release has been associated with decrease in symptoms of patients with cervicogenic headache. This study will be a randomized clinical trial with the sample size of 32 patients. Participants will be randomly allocated into two groups: Group A and Group B. The setting of the study will be Bahawal Victoria Hospital, Bahawalpur. Group A will receive Jones technique of trigger points of the upper trapezius and sternocleidomastoid muscle while Group B will receive ischemic compression of the trigger points of the upper trapezius and sternocleidomastoid muscle. Patients of both groups will receive two treatment sessions per week for 6 weeks. Both groups will receive hot pack for 10 minutes, TENS for 15 minutes and strengthening exercises for deep neck flexors (chin tuck and head raise with ten repetitions of 10-second duration, with a 10-second rest interval between each contraction) as baseline treatment protocol. NPRS, HDI and FRT will be used as outcome measure tools. Data will be analyzed using SPSS version 25.0 with the p-value of \<0.05 taken as significant difference.

This description comes directly from the study's public registry record.

Talk to the study team

Imran Amjad, PHD*  ·  03324390125  ·  imran.amjad@riphah.edu.pk

Imran Amjad, PHD*  ·  0515481826  ·  imran.amjad@riphah.edu.pk

Always discuss trial participation with your own doctor first.

Locations (1)

Bahaval Victoria HospitalBahawalpur, Punjab Province, PakistanRecruiting

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Source record: clinicaltrials.gov/study/NCT06875869