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

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age20-60
SponsorCairo University

About this trial

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

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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)

Disqualifiers

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,

Trial design

Design model

Parallel

Treatments tested in this trial

  • Integrated Neuromuscular Inhibition Technique

    Other intervention

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

  • Postural Correction Exercise

    Other intervention

    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.

Treatment groups

90 Participants
are divided into 2 treatment groups
Group A: Integrated Neuromuscular Inhibition TechniqueExperimental treatment 2 interventions
Group B: Postural Correction ExerciseActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

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 .

Time frame
up to six weeks
2

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.

Time frame
up to 6 weeks

Secondary outcomes

1

pressure pain threshold

pressure pain threshold pressure pain threshold will be assessed by commander algometer

Time frame
up to 6 weeks
2

cervical range of motion

range of motion will be measured by inclinometer CROM. The CROM (deluxe version - Performance Attainment Associates, Roseville, MN, USA) measures the cervical range of motion5- for fexion, extension, lateral fexion, and rotation using separate inclinometers. These inclinometers are attached to a frame similar to that for eyeglasses one in the sagittal plane for fexion - extension, second in the frontal plane for lateral fexion and a third in the horizontal plane for rotation.

Time frame
up to 6 weeks
3

headache frequency

the number of days the subjects feel headache (headache frequency).

Time frame
up to six weeks
4

medication intake

from the patients' diary in the last week , medications intake will be recorded as follow: 1) not at all; 2) once a week; 3) once every couple of days; 4) once or twice a day; or 5) three or more times a day

Time frame
up to six weeks

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: