- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04263389
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
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Cairo
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Giza, Cairo, Egypt, 12613
- Faculty of Physical Therapy, Cairo University
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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 |
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control group
control group is a normal matched group.
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study group
study group is a group of chronic mechanical cervical pain
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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
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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.
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during the procedure
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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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