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About
A randomized controlled trial (RCT) with a pre-test and post-test design will be conducted to compare the therapeutic effectiveness of Dry Needling (DN), Acupressure Therapy (AT), and their combination (DN + AT) against a control group receiving Hot Pack Therapy in patients diagnosed with Cervicogenic Headache (CH).
This study follows the CONSORT (Consolidated Standards of Reporting Trials) guidelines to ensure methodological transparency and rigor. The trial design includes:
Full description
Study Duration Total Duration: 1 year Intervention Period: 2 weeks Follow-Up: Pre-test, post-test, and 2-week follow-up Intervention Procedures
Group A (Dry Needling Therapy - DN)
Group B (Acupressure Therapy - AT)
Group C (Combined Therapy - DN + AT)
Group D (Control - Hot Pack Therapy)
Enrollment
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Inclusion and exclusion criteria
Inclusion Criteria:
Male and female patients aged 20 to 50 years Diagnosed with Cervicogenic Headache (CGH) based on International Headache Society (IHS) diagnostic criteria Chronic CGH symptoms (i.e., persisting for at least 3 months) No previous dry needling (DN) or acupressure therapy (AT) within the last 6 months Able and willing to provide informed consent and comply with treatment and follow-up protocols
Exclusion Criteria: History of cervical spine surgery, significant trauma, or vertebral tumors/neoplasms Congenital spinal deformities (e.g., scoliosis, spina bifida) Diagnosed with cervical radiculopathy, vestibular disorders, vertebrobasilar insufficiency, or cervical fractures Current use of anti-inflammatory drugs, muscle relaxants, or analgesics that may affect pain perception Diagnosed neurological, musculoskeletal, or orthopaedic conditions that affect balance, gait, or functional mobility Pregnancy (optional, often excluded in physiotherapy/dry needling trials)
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80 participants in 4 patient groups
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Data sourced from clinicaltrials.gov
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