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Clinical Trials/NCT06932510
NCT06932510Enrolling By InvitationNot Applicable

EFFECTS OF INFLATTABLE CERVICAL TRACTION COLLAR AS COMPARED TO MANUAL TRACION IN THE MANAGEMENT OF CERVICAL RADICULOPATHY

Foundation University Islamabad1 site in 1 country40 target enrollmentStarted: April 25, 2025Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Enrolling By Invitation
Enrollment
40
Locations
1
Primary Endpoint
Neck Pain

Study Overview

Brief Summary

This study is a randomized control trial and the purpose of this study is to determine the effects of inflatable cervical traction collar as compared to manual traction in the management of cervical radiculopathy.

Detailed Description

The purpose of this study is to determine the effects of inflatable cervical traction collar as compared to manual traction in the management of cervical radiculopathy on

  1. Pain
  2. Functional Disability
  3. Range of motion Data collection procedure: Participants of interest would be approached and explained about the research. Informed written consent will be taken. Recruited participants will be allocated to either of the groups through a sealed opaque envelope method.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Investigator, Outcomes Assessor)

Masking Description

Investigator and outcome assessor are blind to group allocation.

Eligibility Criteria

Ages
19 Years to 44 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Adults aged 19-44 years Neck pain >4 and <8 on NPRS NDI scoring <24(moderate disability) Positive Spurling test Positive Distraction Test Active and passive ROM limited/painful towards the side of pain Radiating Symptoms Numbness/paresthesia radiating to upper limb Both genders Positive - Upper Limb Neural Tension Tests (ULNTT) will be included. -

Exclusion Criteria

  • •Patients having Bilateral radiating sign and symptoms Cervical myelopathy Cervical syringomyelia Rheumatoid arthritis Thoracic outlet syndrome Brachial plexopathy Cervical Rib Vertebrobasilar insufficiency Recent history of fracture, surgery, trauma or whiplash Positive alar ligament stress test Positive sharp purser stress test Cervical instability Cancer, tumor or sudden weight loss.

Arms & Interventions

Manual Traction

Active Comparator

"Manual Traction Group" will be given Manual Traction with facet joint and Upper Extremity Neural Mobilization with Hot Pack and electrotherapy for 20 minutes.

Intervention: Manual Traction (Procedure)

Cervical Traction Collar

Experimental

"Cervical Traction Collar" will be given Manual Traction with facet joint and Upper Extremity Neural Mobilization with Hot Pack and electrotherapy for 20 minutes.

Intervention: Cervical Traction Collar (Device)

Outcomes

Primary Outcomes

Neck Pain

Time Frame: 2 weeks

Neck pain will be measured using Visual Analogue Scale, which has scoring from 0 to 100 mm, and a higher score represents greater pain and a lower score represents less pain.

Neck Disability Index

Time Frame: 2 weeks

It consists of 10 items, each scored on a scale of 0-5, with 0 indicating no pain or limitations and 5 indicating the worst imaginable pain or limitation. The total score ranges from 0-50, with higher score indicating greater disability. The score can also be expressed in terms of percentage.

Cervical Range of Motion

Time Frame: 2 weeks

Cervical range of motion will be measured using a Goniometer. A higher score represents greater range of motion, and lower score represents decreased or lesser range of morion of cervical spine.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Muhammad Osama

Assistant Professor

Foundation University Islamabad

Study Sites (1)

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