NCT07086898

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

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
90

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jul 2025

Shorter than P25 for not_applicable

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

July 18, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

July 25, 2025

Completed
5 days until next milestone

Study Start

First participant enrolled

July 30, 2025

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 25, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

February 25, 2026

Completed
Last Updated

July 25, 2025

Status Verified

July 1, 2025

Enrollment Period

7 months

First QC Date

July 18, 2025

Last Update Submit

July 18, 2025

Conditions

Keywords

integrated neuromuscular inhibition techniquepostural correction exercisescervicogenic headache

Outcome Measures

Primary Outcomes (2)

  • pain intensity

    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 .

    up to six weeks

  • headache disability

    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.

    up to 6 weeks

Secondary Outcomes (5)

  • 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

Study Arms (2)

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

Other: Integrated Neuromuscular Inhibition TechniqueOther: Postural Correction Exercise

Postural Correction Exercise

ACTIVE COMPARATOR

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

Other: Postural Correction Exercise

Interventions

Patients will receive integrated neuromuscular inhibition technique in the form of intermittent ischemic compression, strain counterstrain, and muscle energy technique plus postural correction exercises

Integrated Neuromuscular Inhibition Technique

The exercise program will be in the form of stretching exercises for the sternocleidomastoids (SCM), the scalenes, and upper fibers of trapezius; strengthening isometric exercises for the neck flexors, extensors, lateral flexors, and neck rotators; and postural correction exercises.

Integrated Neuromuscular Inhibition TechniquePostural Correction Exercise

Eligibility Criteria

Age20 Years - 60 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • 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

You may not qualify if:

  • 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,
  • previous

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Post-Traumatic Headache

Condition Hierarchy (Ancestors)

Headache Disorders, SecondaryHeadache DisordersBrain DiseasesCentral Nervous System DiseasesNervous System Diseases

Central Study Contacts

alshaymaa abd elazeim, phd

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Masking Details
opaque sealed envelope
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: integrated neuromuscular inhibition technique and postural correction exercises
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
principle investigator : alshaymaa shaaban abd el azeim

Study Record Dates

First Submitted

July 18, 2025

First Posted

July 25, 2025

Study Start

July 30, 2025

Primary Completion

February 25, 2026

Study Completion

February 25, 2026

Last Updated

July 25, 2025

Record last verified: 2025-07