Effects of Kinesiotherapy Exercises With Cervical Mobilization in Cervicobrachial Neuralgia

June 13, 2024 updated by: Riphah International University

Effects of Kinesiotherapy Exercises Along With Cervical Mobilization in Cervicobrachial Neuralgia.

To evaluate the effects of kinesiotherapy exercises with cervical mobilization in Cervicobrachial Neuralgia.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Detailed Description

Cervicobrachial Neuralgia is characterized by pain and discomfort in the arm, specifically in conjunction with pain in the cervical spine. It has been observed that a significant number of patients seeking therapy for cervical spine diseases are affected by this type of pain. When an illness is chronic, it has a tendency to manifest as a persistent or recurring issue that has a negative impact on an individual's mental and physical well-being.

It is a randomized clinical trial. 30 patients fulfilling the inclusion and exclusion criteria will be recruited by non-probability convenience sampling and then randomly divided in two groups using lottery method. Group A will receive the strengthening and kinesiotherapy exercises along with Brugger's relief position training with 10 minutes per session and cervical lateral glide mobilization, 3 times a week. And the group B will receive the cervical lateral glide mobilization. Pain levels will be measured using a visual analogue scale and goniometer will be used to measure neck ranges.The data will be analyzed by using SPSS version25.

Study Type

Interventional

Enrollment (Estimated)

30

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 Contact

Study Contact Backup

Study Locations

  • Pakistan
    • Punjab
      • Rawalpindi, Punjab, Pakistan, 46000
        • Recruiting
        • IIMCT Railway General Hospital
        • Contact:
        • Principal Investigator:
          • Tuba Ali, MS(OMPT)

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

  • Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Both male and female
  • Age: 30-50 years
  • Positive upper limb neurodynamic test
  • Patients having neck pain radiating to upper limb and limited ROM with articular dysfunction.

Exclusion Criteria:

  • Patients diagnosed with fibromyalgia
  • Surgery of cervical/thoracic spine
  • Limited glenohumeral joint movement
  • Presence of neurological disease (stroke, multiple sclerosis)

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: Kinesiotherapy exercises with cervical mobilization
This group will receive kinesiotherapy exercises along with Cervical Mobilization
Procedure: kinesiotherapy exercises with cervical mobilization
Kinesiotherapy Exercises includes Neck stretches , shoulder and upper back mobility, pectoral stretch, cervical isometrics, shoulder blade protraction and retraction
Procedure: cervical Mobilization
This includes Cervical lateral glide mobilization
Active Comparator: Cervical Mobilization
This group will receive Cervical lateral glide mobilization.
Procedure: kinesiotherapy exercises with cervical mobilization
Kinesiotherapy Exercises includes Neck stretches , shoulder and upper back mobility, pectoral stretch, cervical isometrics, shoulder blade protraction and retraction
Procedure: cervical Mobilization
This includes Cervical lateral glide mobilization

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pain: Visual analogue scale (VAS)
Time Frame: 3 weeks
VAS is a psychometric instrument used to measure subjective characteristics or attitudes, typically pain intensity or other subjective experiences.
3 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Range of Motion: Goniometer
Time Frame: 3 weeks
It is an instrument used to measure angles, typically the range of motion of joints in the human body.
3 weeks

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Cervical radiculopathy impact scale (CRIS)
Time Frame: 3 weeks

It is a 21-item self-reported questionnaire that is used to assess the impact of cervical radiculopathy on patients' daily lives. It is divided into three subscales:

  • Symptoms (9 items)
  • Energy and postures (6 items)
  • Actions and activities (6 items)
3 weeks

Collaborators and Investigators

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

Sponsor

Riphah International University

Investigators

  • Principal Investigator: Rabiya Noor, PhD, Riphah International University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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)

November 23, 2023

Primary Completion (Estimated)

July 1, 2024

Study Completion (Estimated)

July 1, 2024

Study Registration Dates

First Submitted

June 11, 2024

First Submitted That Met QC Criteria

June 13, 2024

First Posted (Actual)

June 14, 2024

Study Record Updates

Last Update Posted (Actual)

June 14, 2024

Last Update Submitted That Met QC Criteria

June 13, 2024

Last Verified

June 1, 2024

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • REC/RCR&AHS/23/01116

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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