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NOT YET RECRUITING
NCT06689371
NA

Dry Needling Versus Dry Cupping on Pain and Disability in Cervicogenic Headache Patients

Sponsor: Cairo University

View on ClinicalTrials.gov

Summary

This study aims to compare the added effects of dry needling and dry cupping to conventional physical therapy on headache pain intensity, headache frequency, headache duration, upper cervical range of motion, and disability levels in patients with cervicogenic headache. It will be assumed that: * All patients will follow all the given instructions strictly during the study duration, regarding the assessment and the treatment procedure. * All participants will be evaluated under the same environmental conditions.

Key Details

Gender

All

Age Range

25 Years - 45 Years

Study Type

INTERVENTIONAL

Enrollment

45

Start Date

2024-11-13

Completion Date

2025-02-01

Last Updated

2024-11-14

Healthy Volunteers

Yes

Interventions

OTHER

Group A (Dry Needling)

The patient will receive dry needling on suboccipital, upper trapezius and SCM muscles with conventional therapy 3 sessions per week for 4 weeks.

OTHER

Group B (Dry cupping)

Patients will receive dry cupping on suboccipital, upper trapezius and SCM muscles weeks with conventional therapy 3 sessions per week for 4 weeks.

OTHER

Group C (control)

will receive standard exercise three sessions per week for four weeks. This standard regimen consists of the same exercises as group A and B.