Effects Of Dry Needling On Sternocleidomastoid Muscle For Pain And Disability In Migraine

Not Applicable

Completed

• Conditions: Migraine
• Interventions: Other: Placebo Dry Needling; Other: Dry Needling

• Registration Number: NCT05285852
• Lead Sponsor: Riphah International University

Brief Summary

To determine the effects, sequel of dry needling in migraine by resolving MTrPs in sternocleidomastoid muscle.

To determine the possession of dry needling technique to mitigate the frequency, intensity and duration of headache.

To determine the effectiveness of dry needling in the disability hindrance in migraine patients.

Detailed Description

This is a randomized control study of 60 volunteers with migraine induced by myofacial triggers in sternocleidomastoid muscle. The migraine will be diagnosed by the neurologist and for the evaluation of trigger points and muscle thickness ultrasound will be done. After the diagnostic procedure and complete history evaluation from the selected population 30 subjects will be subjected to dry needling group and 30 others will be kept in the placebo group. All the participants will receive six sessions at the myofascial trigger point area there should be the gap of at least 48 hours between two sessions. As for the assessment details, such as the frequency, intensity and duration of the headaches; the consumption of drugs; the thickness of SCM muscles; the pain pressure threshold and the cervical range motions will be recorded before, immediately following the response, and at the 1-month follow-up

Study Timeline

• Study Start: 2021-03-01
• Study First Submitted: 2022-03-08
• Study First Submitted QC: 2022-03-08
• Study First Posted: 2022-03-18
• Status Verified: 2022-05
• Primary Completion: 2022-05-15
• Study Completion: 2022-05-15
• Last Update Submitted: 2022-05-18
• Last Update Posted: 2022-05-19

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

• Submitted with a headache diagnosis by a neurologist.
• Presence of active Trigger points in the Sternocleidomastoid muscle reproducing the symptoms of migraine.
• Active trigger points will be identified if "there is muscle sensitivity that has been activated by pressure and reproduces the patient's referred pain and headache."
• A jump sign the characteristic behavioral response to compression on a trigger point, will be produced.

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Exclusion Criteria

• background of neck trauma
• cervical radiculopathy
• History of head/shoulder surgery
• Diagnosis of other unusual headaches/migraines
• Phobia of pricking
• pregnancy

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Placebo Dry Needling	Placebo Dry Needling	Following identification of the trigger point in the muscle, the surface would be cleaned with an antiseptic solution. For placebo Dry Needling, which only causes a pricking sensation, a blunt needle will be applied to the trigger points without penetrating the skin after application of a certain pressure to the skin. The protocol will be applied six times, with a two-day pause between treatments. Like the intervention group, the variables will be measured immediately after the processing session.
Dry Needling	Dry Needling	For application of the Dry Needling the individual should be in the supine position. To facilitate the approach and adhesion of the Sternocleidomastoid Muscle, the person's neck is placed ipsilaterally in the slightly lateral flexed position. Consequently, the therapist identified the active Trigger Points in the Sternocleidomastoid Muscle and cleansed the surface using an antiseptic solution. Using the insertion pipe, the dry needle inserted into the muscle. For the separation of neurovascular structure from muscle belly the needle is carried out in an anterior-posterior direction. A compression of 90 secs with a cotton swab will be applied at the needling site immediately after removing the needle to reduce the intensity and duration of pain. The variables will then be measured immediately following the processing session. Six sessions of Dry Needling will be applied to each patient and there will be a gap of at least 48 hours between each session.

Primary Outcome Measures

Name	Time	Method
Sternocleidomastoid muscle Ultrasonography	12th Week	An ultrasonograph scan uses high-frequency sound waves to make an image of a person's internal body structures
Visual Analogue Scale	12th Week	A Visual Analogue Scale is a measurement instrument that tries to measure a characteristic or attitude that is believed to range across a continuum of values and cannot easily be directly measured. It is often used in epidemiologic and clinical research to measure the intensity or frequency of various symptoms.
Bubble Inclinometer	12th Week	Bubble Inclinometer is a simple to use device for measuring range of motion in patients. The inclinometer can be used to measure range of motion in the neck, the hip, the elbow, the knee, the shoulder, the spine, the ankle, the wrist, and the Metacarpophalangeal joint.

Trial Locations

Locations (1)

Ripah International University; 🇵🇰 Faisalabad, Punjab, Pakistan