Quantitative Assessment of Shoulder Proprioception in Patients With Chronic Mechanical Cervical Pain

July 19, 2022 updated by: Hamada Ahmed
The study was aimed to compare shoulder proprioception in chronic mechanical cervical pain to a matched normal group. This study include 2 groups, 40 subjects with mechanical chronic cervical pain and 40 healthy subjects representing the control group. The primary outcome measure was the shoulder proprioception test of both upper limbs during active repositioning and quantified with angular displacement error.

Study Overview

Status

Completed

Conditions

Detailed Description

The study was aimed to compare shoulder proprioception in chronic mechanical cervical pain to a matched normal group. This study include two groups, 40 subjects with mechanical chronic cervical pain and 40 healthy subjects representing the control group. The primary outcome measure was the shoulder proprioception test of both upper limbs during active repositioning and quantified with angular displacement error. Test was applied using an isokinetic dynamometer device at angle 30° for both shoulder internal and external rotation on both sides with an angular velocity 30°/sec.

Study Type

Observational

Enrollment (Actual)

80

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

    • Cairo
      • Giza, Cairo, Egypt, 12613
        • Faculty of Physical Therapy, 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

20 years to 35 years (Adult)

Accepts Healthy Volunteers

N/A

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

For the control group they are normal subjects. For the group with cervical pain, participants had a chronic mechanical cervical pain started from three to 12 months with a score of 3 to 65 according to the short-form of the McGill Pain Questionnaire (SF-MPQ).

Description

Inclusion Criteria:

  • The age ranged from 20 to 35 years.
  • Body Mass Index (BMI) between 18 and less than 30.
  • Sufficient cognitive abilities that enables them to understand and follow instructions with a score more than 24 in the Mini-Mental State Examination (MMSE) scale.
  • For the group with cervical pain, participants had a chronic mechanical cervical pain started from three to 12 months.
  • Participants with chronic pain with a score of 3 to 65 according to the short-form of the McGill Pain Questionnaire (SF-MPQ).

Exclusion Criteria:

  • Shoulder problems.
  • Previous cervical or shoulder surgery.
  • Shoulder or cervical trauma.
  • Cervical radiculopathy.
  • Sever visual and/or auditory problems.
  • Cognitive impairment (a score less than 24 according to MMSE).

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

Cohorts and Interventions

Group / Cohort
control group
control group is a normal matched group.
study group
study group is a group of chronic mechanical cervical pain

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Absolute angular error (AAE) of shoulder joint
Time Frame: during the procedure
The AAE is an angle that was measured using the isokinetic dynamometer to indicate the sense of position for shoulder joint. Two measurements were performed; AAE for external rotation range and AAE for internal rotation range for both right and left arms.
during the procedure

Collaborators and Investigators

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

Sponsor

Collaborators

Investigators

  • Study Director: Wael Shendy, PhD, Associate professor Faculty of Physical Therapy-Cairo University

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)

April 1, 2019

Primary Completion (Actual)

November 15, 2019

Study Completion (Actual)

December 30, 2019

Study Registration Dates

First Submitted

January 24, 2020

First Submitted That Met QC Criteria

February 7, 2020

First Posted (Actual)

February 10, 2020

Study Record Updates

Last Update Posted (Actual)

July 22, 2022

Last Update Submitted That Met QC Criteria

July 19, 2022

Last Verified

February 1, 2020

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • P.T.Rec/012/002078

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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