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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04263389
Other study ID # P.T.Rec/012/002078
Secondary ID
Status Completed
Phase
First received
Last updated
Start date April 1, 2019
Est. completion date December 30, 2019

Study information

Verified date February 2020
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 80
Est. completion date December 30, 2019
Est. primary completion date November 15, 2019
Accepts healthy volunteers
Gender All
Age group 20 Years to 35 Years
Eligibility 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 Design


Related Conditions & MeSH terms


Locations

Country Name City State
Egypt Faculty of Physical Therapy, Cairo University Giza Cairo

Sponsors (2)

Lead Sponsor Collaborator
Hamada Ahmed Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Absolute angular error (AAE) of shoulder joint 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
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