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

H

Hamada Ahmed

Status

Completed

Conditions

Cervical Pain

Study type

Observational

Funder types

Other

Identifiers

NCT04263389
P.T.Rec/012/002078

Details and patient eligibility

About

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.

Full 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.

Enrollment

80 patients

Sex

All

Ages

20 to 35 years old

Volunteers

No Healthy Volunteers

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).

Trial design

80 participants in 2 patient groups

control group
Description:
control group is a normal matched group.
study group
Description:
study group is a group of chronic mechanical cervical pain

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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