MedPath

Effects of ELDOA in Patients With Cervicogenic Headache

Not Applicable
Completed
Conditions
Cervicogenic Headache
Interventions
Other: conventional therapy
Other: ELDOA and conventional therapy
Registration Number
NCT06377787
Lead Sponsor
Riphah International University
Brief Summary

The aim of our study is to determine the effect of ELDOA in relieving pain, improving ROM and functional disability in patients with cervicogenic headache. This study will add to the growing body of knowledge that if this technique yields comparable outcomes, it would be the alternative therapy. Moreover, it would add to the society as no literature is available on the effect of ELDOA technique in the management of Cervicogenic headache.

Detailed Description

Cervicogenic Headache (CEH) is mainly caused by neck or paravertebral soft tissue lesions. It is chronic headache that arises from the Atlanto-occipital and upper cervical joints and is perceived in one or more regions of the head or face. One of the known treatment options that create decompression at spinal segment level is called ELDOA it is described as a conditioning method involving a series of movements and body stretches to help correct body posture, rehabilitate people with injuries and prevent injuries

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
24
Inclusion Criteria
  • Age: 30-45 years
  • Both male and female.
  • Onset of pain > 4 weeks.
  • Flexion rotation test positive with estimated rotation range reduced by more than 10 degrees from the anticipated normal range (44 degrees)
  • Tenderness of upper three cervical joints.
  • Presence of active trigger points in upper trapezius and sub occipital extensors.
Read More
Exclusion Criteria
  • Hypertension.
  • Recent (<6 months) whiplash injury and other cervical soft tissue injuries.
  • History of cervical spinal vertebrae fracture.
  • Positive sharp purser test
  • Acute disc protrusion • History of cancer.
  • Previous surgical intervention of head, neck and thoracic spine
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
conventional therapyconventional therapyhot pack and TENS for 10 minutes, cervical PIR (MET) in flexion, extension, side bending and rotation (single set of 4 reps with 6 seconds hold once a day).
ELDOA and conventional therapyELDOA and conventional therapyhot pack and TENS for10 min, cervical PIR (MET) in flexion, extension, side bending and rotation (single set of 4rep with 6 sec hold once a day) and ELDOA method C0-C1-C2, C2 \& C3 positions for cervical spine (2 sets of five repetitions with 45 sec hold and 15sec rest between each set once a day).
Primary Outcome Measures
NameTimeMethod
NDI (U) (Neck Disability Index)four weeks

The neck disability index is a ten-item self-reported questionnaire that assesses pain and associated disability, with a total max score of 50 points . An Urdu version of neck disability index will use in this study. An intra-class correlation coefficient (ICC) revealed excellent test-retest reliability for all items (ICC = 0.86-0.98) and total scores (ICC = 0.99) of the NDI-U.

(Numeric Pain Rating Scale).four weeks

The Numeric Pain Rating Scale (NPRS) measures the subjective intensity of pain. The NPRS is an eleven-point scale from 0 to 10. "0" = no pain and "10" = the most intense pain imaginable while the NPRS exhibited moderate reliability (ICC = 0.27-0.84)

Inclinometerfour weeks

Cervical range of motion will be measured using inclinometer. It is a common instrument used to measure joint range of motion.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Alkhidmat Raazi Hospital CBR Town

🇵🇰

Islamabad, Punjab, Pakistan

© Copyright 2025. All Rights Reserved by MedPath