Deep Neck Flexors Training Versus Muscle Energy Technique on Cervicogenic Headache

March 12, 2024 updated by: Riphah International University

Effects of Deep Neck Flexors Training Versus Muscle Energy Technique on Cervicogenic Headache

Aim of this study is to compare the effects of deep neck flexors stretching versus muscles energy technique on pain, cervical range of motion, sleep disturbance and cervical spine posture in patients with Cervicogenic headache and interpret which technique is better among both.A randomized control trial that will include total 28 participants.The first group will receive deep neck flexors stretching along with conventional therapy and 2nd group will receive muscles energy technique along with conventional therapy.Data collected will be analyzed through SPSS 25.

Study Overview

Detailed Description

Cervicogenic headache is a disabling condition associated with musculoskeletal impairment of the cervical region.Cervicogenic headache is a clinical syndrome characterized by primarily unilateral pain that originates in the neck, typically provoked by neck movement or pressure over tender points in the neck, with reduced range of movement of the cervical spine.Cervicogenic Headache is pain referred to the head from a source in the cervical spine. It can influence the patient's quality of life in addition to a loss of functions when compared with the groups with other headache disorders.

A variety of invasive and noninvasive therapeutic modalities are used in the treatment of cervicogenic headache.Physical therapy is considered as most effective treatment of cervicogenic headache including modalities, manual therapy, muscle stretching, Muscle Energy Techniques, deep neck flexors training, Instrument-Assisted Soft Tissue Mobilization , therapeutic exercises and kinesiology tapping.Deep cervical flexor exercise is a low-load exercise focused on deep cervical flexor muscles, as described by Jull et al. This exercise targets the deep flexor muscles of the cervical region, rather than the superficial flexor muscles. Deep neck flexor training is said to improve the Cervicogenic headache according to the literature review.

According to the Literature review, in cervicogenic headache 2 group of muscles are involved i.e. deep cervical flexors (longus colli, longus capitis, Rectus capitis and Longus capitus) gets weakened and cervical extensors (suboccipital and upper trapezius) gets tightened. It is evident that deep neck flexor training is effective in improving pain, cervical range of motion and posture in Cervicogenic headache. Muscle Energy techniques are also proven to reduce pain and improve range of motion so post isometric relaxation will use in this study. Limited literature is available which compares the effects of post isometric relaxation deep neck flexors and specifically on Cervicogenic headaches. Aim of this study is to compare the effects of these techniques on pain, cervical range of motion, sleep disturbance and cervical spine posture in patients with Cervicogenic headache and interpret which technique is better among both. I hope that this study will add valuable literature and scope for future researchers to work on this topic.

Study Type

Interventional

Enrollment (Actual)

28

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Punjab
      • Rawalpindi, Punjab, Pakistan, 44000
        • Railway General Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 55 years (Adult)

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Subjects aged 18 - 55 years.
  • Both male and female subjects will be recruited in the study.
  • Unilateral headache (without side shift) related by pain, movement and sustaining
  • position of neck started from the occiput spread to the tempro-frontal region for more than 3 months
  • >20 degree movement restriction in cervical ROM, especially in the upper cervical rotation.
  • Positive flexion rotation test to confirm Cervicogenic headache.
  • Subjects with rounded shoulders having distance between on the table and the acromion>2.5 cm

Exclusion Criteria:

  • Fracture or previous surgery on vertebral column
  • History of spinal stenosis or disc prolapse
  • dysfunction or headache with autonomic involvement
  • Other types of headache including migraine, tension type etc.
  • laxity of alar ligaments
  • vertebra basilar artery insufficiency
  • Patients with a history of physiotherapy at least 3 months prior to the study.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: deep neck flexor group

Deep neck flexors stretch

Conventional Therapy:

Moist heat therapy for 10 minutes, TENS 10 min, cervical active ROMS, Non-thrust mobilizations

Hold for 10 sec and repeated 10 times.Patients will be treated 3 times a week for 4 consecutive weeks
Active Comparator: muscle energy technique

Post isometric stretch on trapezious and suboccipital muscles

Conventional Therapy:

Moist heat therapy for 10 minutes, TENS 10 min, cervical active ROMS, Non-thrust mobilizations

position of patient is in maximal comfort and lengthening After engaging the barrier use of an isometric contraction Feel the release and lengthen the muscle repeated for 4 time per session Patients will be treated 3 times a week for 4 consecutive weeks

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Numeric Pain rating scale
Time Frame: 4 weeks
The Numeric Pain Rating Scale (NPRS) measures the subjective intensity of pain.
4 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Inclinometer
Time Frame: 4 weeks
Measurements of cervical flexion, extension, lateral flexion, and rotation will be measured using inclinometer
4 weeks
Cervical posture
Time Frame: 4 weeks
For measurement of cervical posture, photographs taken from the side were used for objective measurement of forward head posture
4 weeks
Insomnia Severity Index (ISI)
Time Frame: 4 weeks
It is a brief self-report questionnaire that measures the patient's perception of insomnia severity
4 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Madiha Ali, MSOPMT, Riphah International University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 15, 2023

Primary Completion (Actual)

August 15, 2023

Study Completion (Actual)

September 15, 2023

Study Registration Dates

First Submitted

February 23, 2023

First Submitted That Met QC Criteria

February 23, 2023

First Posted (Actual)

March 6, 2023

Study Record Updates

Last Update Posted (Actual)

March 13, 2024

Last Update Submitted That Met QC Criteria

March 12, 2024

Last Verified

March 1, 2024

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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