The Relationship Between Cervical Radiculopathy and Eye-hand Coordination (CR)

December 11, 2023 updated by: Basma Saeed Ibrahim el Gabry, Cairo University
this study will be conducted to investigate if there is a relationship between cervical radiculopathy and eye-hand coordination.

Study Overview

Status

Not yet recruiting

Detailed Description

Cervical radiculopathy is a disorder involving dysfunction of the cervical nerve roots commonly secondary to cervical spine degenerative changes such as disk herniation and/or foraminal stenosis compressing the nerve roots. Clinical manifestations are pain in neck and one or both of the upper extremities, as a result of compression or irritation of nerve roots in the cervical spine. It can be accompanied by motor, sensory, or reflex deficits. It is most common in persons 45-60 years of age, which result in terrible chronic pain. Eye hand coordination is the ability to do activities which require the simultaneous use of hands and eyes. It is a complex cognitive skill which unites visual and motor skills in the person and allowing the hands to guide by the visual stimulations. It lies at the core of our daily activities and interactions with objects and people around us as to be a defining characteristic of typical human life. Previous studies show that there was a marked alteration in the hand function in subjects with the cervical radiating pain. Since there was no study which investigated the relationship between cervical radiculopathy and eye hand coordination despite it is an important skill that adults use in countless activities of daily living and during working.

Study Type

Observational

Enrollment (Estimated)

60

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

Yes

Sampling Method

Non-Probability Sample

Study Population

the first population will be thirty with cervical radiculopathy, the second group will be thirty subjects with the normal state

Description

Inclusion Criteria:

  • Subjects normal with no neck complain.
  • Patients of cervical radiculopathy due to cervical discogenic lesion.
  • Ages range from 30-50 both males and females.
  • Subjects should be able to follow simple verbal commands or instructions included in the procedures.

Exclusion Criteria:

  • Participants with any neck trauma.
  • Cervical Post-operative patients.
  • Participants with vision deficiency.
  • Participants with perceptual and cognitive problems with score less than 24 in mini mental state scale (Appendix I) (Goudsmit et al., 2018).
  • Participants with any other neurological or musculoskeletal problems.
  • Participants take medications that affect their attention.
  • Participants have space-occupying lesions eg. tumors

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
Intervention / Treatment
cervical radiculopathy group
thirty participants with cervical radiculopathy due to discogenic lesions.
this group will have patients with cervical radiculopathy
normal group
thirty participants in normal without any discogenic lesion
this group will have normal subjects

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
eye hand coordination movement speed objectively
Time Frame: baseline
The Purdue Pegboard test will be used to assess eye hand coordination speed by putting as many pins as possible into the pegboard in 30 sec. the Test will be done three times each and averaged. The score for each of the four subtests
baseline
pain intensity
Time Frame: baseline
numerical pain rating scale will be used for assessment of pain intensity. It is a single 11-point numeric scale. The physical therapist will ask the patient to state a number from 1 to 10 that best represents their perceived current pain intensity or pain intensity "in the last 24 hours". Zero usually represents 'no pain at all' whereas 10 is the upper limit represents 'the worst pain ever possible'
baseline
eye hand coordination accuracy and timing
Time Frame: baseline
talking pen test will used to assess the accuracy and timing; Patient will grasp the pen like any writing tool with the thumb, index finger and middle finger. Patient will hold the pen at no less than a 45 angle from the writing space. An infra-red light and fiber optic sensor in the tip of the pen sense reflect as the user traces a pattern with the pen and provide immediate auditory feedback if the user wanders off the pattern.
baseline
eye hand coordination movement speed subjectively
Time Frame: baseline
wall catch test will be used to assess eye hand coordination movement speed;A bucket of tennis balls will be available directly in front of the participant and a ball will be held in the dominant hand. The physical therapist will count down '3, 2, 1, go' and start the stopwatch, the ball will be thrown underarm off the wall and the return will be caught in their opposing hand. The participant then continue to throw and catch the ball in alternative hands for 30 s. If a ball is dropped, participants will be instructed to reach into the bucket of balls and to continue the test as quickly as possible.
baseline
eye hand coordination upper and limb muscles coordination
Time Frame: baseline
standardized finger to nose test will be used to assess eye hand coordination upper and limb muscles coordination; Test will be performed with patient starting position then the patient will be asked to bring the tip of index finger to the tip of his nose then to touch a target 45 cm at arm's length and return to touch their nose again. It consists of recording how many times the individuals alternately touched their tip of their nose and a target placed in front of them on a wall
baseline

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 (Estimated)

December 20, 2023

Primary Completion (Estimated)

January 20, 2024

Study Completion (Estimated)

January 20, 2024

Study Registration Dates

First Submitted

November 5, 2023

First Submitted That Met QC Criteria

December 11, 2023

First Posted (Actual)

December 13, 2023

Study Record Updates

Last Update Posted (Actual)

December 13, 2023

Last Update Submitted That Met QC Criteria

December 11, 2023

Last Verified

December 1, 2023

More Information

Terms related to this study

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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