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Comparison of Cervical Traction Versus Snag to Improve Pain and Quality of Life in Cervical Radiculopathy

Primary Purpose

Quality of Life, Cervical Radiculopathy

Status
Recruiting
Phase
Not Applicable
Locations
Pakistan
Study Type
Interventional
Intervention
Cervical Traction
Snag
Sponsored by
Superior University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Quality of Life

Eligibility Criteria

20 Years - 50 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Males and females were included. Age group 20-50 years. Patient suffering with neck pain radiating down the arms. Patients with positive Spurling test, cervical distraction and upper limb tension test. Exclusion Criteria: Subject suffering with any systemic diseases of MSK. Patients already suffering with pain in shoulder and upper extremity which is of local origin. Patient with cardiovascular or respiratory disease. Patients having osteophytes in cervical vertebrae. Hypermobility of cervical region.

Sites / Locations

  • Chaudary Muhammad Akram Teaching Hospital, Azra Naheed Medical College, Superior UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Experimental

Arm Label

Cervical Traction

Snag Therapy

Arm Description

Outcomes

Primary Outcome Measures

Visual Analog Scale
Quality of Life Scale QOL
QOL to improve Quality of Life in Cervical Radiculopathy

Secondary Outcome Measures

Full Information

First Posted
March 18, 2023
Last Updated
May 10, 2023
Sponsor
Superior University
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1. Study Identification

Unique Protocol Identification Number
NCT05854108
Brief Title
Comparison of Cervical Traction Versus Snag to Improve Pain and Quality of Life in Cervical Radiculopathy
Official Title
Comparison of Cervical Traction Versus Snag to Improve Pain and Quality of Life in Cervical Radiculopathy
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
April 1, 2023 (Actual)
Primary Completion Date
June 1, 2023 (Anticipated)
Study Completion Date
August 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Superior University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
For the wellness by Comparing of Cervical Traction Versus Snag to reduce Pain and improve Quality of Life in Cervical Radiculopathy

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Quality of Life, Cervical Radiculopathy

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Cervical Traction
Arm Type
Other
Arm Title
Snag Therapy
Arm Type
Experimental
Intervention Type
Diagnostic Test
Intervention Name(s)
Cervical Traction
Intervention Description
Cervical Traction to Improve Pain and Quality of Life in Cervical Radiculopathy
Intervention Type
Diagnostic Test
Intervention Name(s)
Snag
Intervention Description
Snag to Improve Pain and Quality of Life in Cervical Radiculopathy
Primary Outcome Measure Information:
Title
Visual Analog Scale
Time Frame
6 Months
Title
Quality of Life Scale QOL
Description
QOL to improve Quality of Life in Cervical Radiculopathy
Time Frame
6 Months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Males and females were included. Age group 20-50 years. Patient suffering with neck pain radiating down the arms. Patients with positive Spurling test, cervical distraction and upper limb tension test. Exclusion Criteria: Subject suffering with any systemic diseases of MSK. Patients already suffering with pain in shoulder and upper extremity which is of local origin. Patient with cardiovascular or respiratory disease. Patients having osteophytes in cervical vertebrae. Hypermobility of cervical region.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ramsha Amjad, DPT
Phone
+923344282683
Email
ramshaamjad2@gmail.com
Facility Information:
Facility Name
Chaudary Muhammad Akram Teaching Hospital, Azra Naheed Medical College, Superior University
City
Lahore
State/Province
Punjab
Country
Pakistan
Individual Site Status
Recruiting

12. IPD Sharing Statement

Plan to Share IPD
No

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Comparison of Cervical Traction Versus Snag to Improve Pain and Quality of Life in Cervical Radiculopathy

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