The Effects of Scapular Muscles Training Using a Suspension System in Patients With Non Spacific Chronic Neck Pain and Scapular Dyskinesia

June 8, 2023 updated by: Nourhan Gamal Khattab, Cairo University
The study aimed to investigate the effect of scapular muscle training using a suspension system in patients with non spacific chronic neck pain with scapular diskinesia

Study Overview

Study Type

Interventional

Enrollment (Actual)

52

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 Locations

      • Giza, Egypt
        • Cairo University

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:

  • Patients age between 20-35 years.
  • Patients with non spacific pain(pain > 3 month).
  • pain must have been present for at least the previous 12 weeks.
  • Patients with non spacific chronic neck pain with scapular dyskinesia.
  • Patient BMI<30.

Exclusion Criteria:

  • History of previous neck surgery.
  • Recent or old fractures.
  • Cognitive impairment and inability to understand the scale.
  • Systematic inflammatory disease e.g., rheumatoid arthritis and ankylosing Spondylitis.
  • Neck pain with radiculopathy or neuropathy.
  • Scapular dyskinesia due to other pathology such as shoulder impingement

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: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Excercise therapy group
The group that recived scapular muscle training exercises
Scapular muscle strength by resistance
Experimental: Suspension group
The group that recived scapular muscle training using suspension system
suspended from the handles of the straps by either their hands or feet while the non-suspended pair of extremities are in contact with the ground leading to muscle activation due to unstable base of support
Other Names:
  • Sling therapy

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Scapular muscle strength
Time Frame: 1week
Scapular muscle strength is measured by hand held dynanometer
1week
Scapular position
Time Frame: 1week
Scapular position is measured by lateral scapular slide test
1week
Pain intensity
Time Frame: 1week
Pain intensity is measured by neumeric pain rating scale the lowest value is 0 means no pain and the highest value is 10 means the worst pain
1week
Function
Time Frame: 1 week
Function is measured by neck disability index the total score is 50 as the score is higher the disability is higher
1 week

Collaborators and Investigators

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

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)

October 1, 2022

Primary Completion (Actual)

May 30, 2023

Study Completion (Actual)

May 30, 2023

Study Registration Dates

First Submitted

May 30, 2023

First Submitted That Met QC Criteria

May 30, 2023

First Posted (Actual)

June 8, 2023

Study Record Updates

Last Update Posted (Actual)

June 12, 2023

Last Update Submitted That Met QC Criteria

June 8, 2023

Last Verified

June 1, 2023

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

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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