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

NCT ID: NCT05854108

Last Updated: 2023-05-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-04-01

Study Completion Date

2023-08-31

Brief Summary

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

Detailed Description

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Conditions

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Quality of Life Cervical Radiculopathy

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

NONE

Study Groups

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Cervical Traction

Group Type OTHER

Cervical Traction

Intervention Type DIAGNOSTIC_TEST

Cervical Traction to Improve Pain and Quality of Life in Cervical Radiculopathy

Snag Therapy

Group Type EXPERIMENTAL

Snag

Intervention Type DIAGNOSTIC_TEST

Snag to Improve Pain and Quality of Life in Cervical Radiculopathy

Interventions

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Cervical Traction

Cervical Traction to Improve Pain and Quality of Life in Cervical Radiculopathy

Intervention Type DIAGNOSTIC_TEST

Snag

Snag to Improve Pain and Quality of Life in Cervical Radiculopathy

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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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.
Minimum Eligible Age

20 Years

Maximum Eligible Age

50 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Superior University

OTHER

Sponsor Role lead

Responsible Party

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Muhammad Naveed Babur

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Chaudary Muhammad Akram Teaching Hospital, Azra Naheed Medical College, Superior University

Lahore, Punjab Province, Pakistan

Site Status RECRUITING

Countries

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Pakistan

Central Contacts

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Ramsha Amjad, DPT

Role: CONTACT

+923344282683

Other Identifiers

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DPT/Batch-Fall18/535

Identifier Type: -

Identifier Source: org_study_id

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