NCT06169618

Brief Summary

this study will be conducted to investigate if there is a relationship between cervical radiculopathy and eye-hand coordination.

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
60

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Dec 2023

Shorter than P25 for all trials

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

November 5, 2023

Completed
1 month until next milestone

First Posted

Study publicly available on registry

December 13, 2023

Completed
7 days until next milestone

Study Start

First participant enrolled

December 20, 2023

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 20, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 20, 2024

Completed
Last Updated

December 13, 2023

Status Verified

December 1, 2023

Enrollment Period

1 month

First QC Date

November 5, 2023

Last Update Submit

December 11, 2023

Conditions

Keywords

eye hand co ordinationcervical radiculopathy

Outcome Measures

Primary Outcomes (5)

  • eye hand coordination movement speed objectively

    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

    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

    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

    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

    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

Study Arms (2)

cervical radiculopathy group

thirty participants with cervical radiculopathy due to discogenic lesions.

Other: cervical radiculopathy

normal group

thirty participants in normal without any discogenic lesion

Other: normal group

Interventions

this group will have patients with cervical radiculopathy

cervical radiculopathy group

this group will have normal subjects

normal group

Eligibility Criteria

Age30 Years - 50 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
Study Population

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

You may qualify if:

  • 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.

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Radiculopathy

Condition Hierarchy (Ancestors)

Peripheral Nervous System DiseasesNeuromuscular DiseasesNervous System Diseases

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
OTHER
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
principle investigator Basma saeed ibrahim el gabry

Study Record Dates

First Submitted

November 5, 2023

First Posted

December 13, 2023

Study Start

December 20, 2023

Primary Completion

January 20, 2024

Study Completion

January 20, 2024

Last Updated

December 13, 2023

Record last verified: 2023-12