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Clinical Trials/NCT07086898
NCT07086898Not yet recruitingNot Applicable

Impact of Adding Integrated Neuromuscular Inhibition Technique to Postural Correction Exercises in Patients With Cervicogenic Headache

Cairo University0 sites90 target enrollmentStarted: July 30, 2025Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
90
Primary Endpoint
pain intensity

Study Overview

Brief Summary

this study will be conducted to investigate the impact of adding integrated neuromuscular inhibition technique to postural correction exercises in patients with cervicogenic headache

Detailed Description

Cervicogenic headache (CeH) is a secondary headache attributed to dysfunctions of the cervical spine. CGH is a non-throbbing, unilateral, side locked headache that originates in the cervical spine and gradually spreads to the occipital, temporal and orbital areas. It is associated with neck pain or stiffness and is often aggravated by sustained neck postures, repeated neck movements or physical activity. INIT is effective as it causes sustained or intermittent compression which causes ischemia reduces local circulation until pressure is released, after which a flushing of fresh oxygenated blood occurs. Mechanoreceptors impulses interface with slower pain messages reducing amount of pain messges reaching the brain, releasing pain relieving hormones, decreasing myofascial pain. Stretches the taut bands of muscles fibers. INIT along with strengthening excercises proved to be beneficial in decreasing disability improving Range of motion.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Masking Description

opaque sealed envelope

Eligibility Criteria

Ages
20 Years to 60 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •20 to 60 years old patient with unilaterally of the head pain
  • •pain triggered by external pressure over the upper cervical joints (c1-c3)
  • •pain elicited by the neck movements, and/or sustained awkward positions with reduced neck ROM
  • •headache intensity pain score of at least 20mm on the Visual analogue scale (VAS)
  • •headache frequency of at least once a week for at least 3 months
  • •minimum neck disability index score of 10 points or greater

Exclusion Criteria

  • •Migraine, tension- type headache, tumor, osteoporosis, fracture, rheumatoid arthritis and metabolic diseases.
  • •Prolonged history of steroid use.
  • •Resting blood pressure greater than 140/90 mmhg.
  • •cervical spinal stenosis, diminished sensation and central nervous system involvement,

Arms & Interventions

Integrated Neuromuscular Inhibition Technique

Experimental

Forty-five patients will receive integrated neuromuscular inhibition technique plus postural correction exercises three times a week for six weeks

Intervention: Integrated Neuromuscular Inhibition Technique (Other)

Integrated Neuromuscular Inhibition Technique

Experimental

Forty-five patients will receive integrated neuromuscular inhibition technique plus postural correction exercises three times a week for six weeks

Intervention: Postural Correction Exercise (Other)

Postural Correction Exercise

Active Comparator

Forty-five patients will receive postural correction exercises three times a week for six weeks

Intervention: Postural Correction Exercise (Other)

Outcomes

Primary Outcomes

pain intensity

Time Frame: up to six weeks

visual analogue scale will be used to asses pain intensity which patient will be instructed to put point on line from no pain to tolerable pain. The scale consists of a line, usually 100 mm long, ranging from no pain or discomfort (zero) , to the worst pain that could possibly feel .

headache disability

Time Frame: up to 6 weeks

The Headache spesific Disability Questionnaire was used to assess headcahe disability. it is a self-administered scale with 9 items that assesses pain intensity, work or school disruptions, and the effect on recreational activities in individuals with headache complaints. Higher scores reflect greater impairment.

pain intensity

Time Frame: up to six weeks

visual analogue scale will be used to asses pain intensity which patient will be instructed to put point on line from no pain to tolerable pain. The scale consists of a line, usually 100 mm long, ranging from no pain or discomfort (zero) , to the worst pain that could possibly feel .

headache disability

Time Frame: up to 6 weeks

The Headache spesific Disability Questionnaire was used to assess headcahe disability. it is a self-administered scale with 9 items that assesses pain intensity, work or school disruptions, and the effect on recreational activities in individuals with headache complaints. Higher scores reflect greater impairment.

Secondary Outcomes

  • pressure pain threshold(up to 6 weeks)
  • cervical range of motion(up to 6 weeks)
  • headache frequency(up to six weeks)
  • medication intake(up to six weeks)
  • headache duration(up to six weeks)
  • pressure pain threshold(up to 6 weeks)
  • cervical range of motion(up to 6 weeks)
  • headache frequency(up to six weeks)
  • medication intake(up to six weeks)
  • headache duration(up to six weeks)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Al Shaymaa Shaaban Abd El Azeim

principle investigator : alshaymaa shaaban abd el azeim

Cairo University

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