The Effect Of Cervical Muscle Fatigue in Neck Proprioception and Postural Stability

June 16, 2020 updated by: Alaa Yousri Mahmoud Atia

The Effect of Cervical Muscle Fatigue on Neck Proprioception and Postural Stability

PURPOSE:

To investigate the effect of cervical muscle Fatigue on neck proprioception and postural stability during cervical flexion.

BACKGROUND:

Postural stability is the ability to maintain the body in equilibrium either at rest or in a steady state of motion . Muscle fatigue is the diminished response of muscle to repeated stimulus. Cervical proprioceptive inputs provide important somatosensory information influencing postural stability. Hence, the investigators performed this study to evaluate the effect of experimentally induced fatigue on general cervical musculature on postural stability .

HYPOTHESES:

This study will hypnotize that:

  1. Cervical flexor muscle fatigue will have a significant effect on neck proprioception
  2. Cervical muscle fatigue will have a significant effect on posture stability

RESEARCH QUESTION:

Will fatigue of cervical flexors have an effect on neck proprioception and postural stability?

Study Overview

Status

Unknown

Conditions

Intervention / Treatment

Detailed Description

the research methodology that will be used

Induction of fatigue using isometric neck flexor muscle endurance test (NET):

An isometric neck muscle endurance test (NME test) will be performed for the deep neck flexors (Rectus Capitus Anterior, Rectus Capitus Lateralis, Longus Capitus, Longus Colli) until exhaustion in all participants occurs. With the subject in hook lying position through CHIN RETRACTION AND HEAD ELEVATED FROM THE COUCH.

All the assessment measurements will be done before and just immediately after performing the cervical muscle fatigue then after 15 minutes of fatigue induction(fatigue recovery) A. Measurement of neck proprioception using cervical joint position error test via OVERHEAD LASER POINTER

B. Measurement of postural stability using :

  1. Biodex balance system(limit of stability) to measure postural stability
  2. Multi-Directional Reach Test

Study Type

Observational

Enrollment (Anticipated)

45

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

    • Giza
      • Cairo, Giza, Egypt, 00202
        • Recruiting
        • Ministry of Health
        • Contact:

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

18 years to 40 years (Adult)

Accepts Healthy Volunteers

N/A

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

Residents from certain town

Description

Inclusion Criteria:

  • having cervical range of motion 80 to 90 of flextion, 70 degree of extension, 20 to 45 degrees if lateral flextion, and 80 to 90 rotation to both sides.
  • having normaluscle test strength for cervical neck flexors according to group manual muscle test
  • body mass index ranging from 18.5 to 24.9 kg/m2

Exclusion Criteria:

  • any history of pathological truma to the cervical,thoracic or lumbar spine, upper extremity or rib cage.
  • surgical condition of the spine
  • having any orthopedic, musculoskeletal or neurological disorders around cervical region.
  • any vestibular impairment (e.g.vertigo)
  • spinal postural deformities as hyper kyphosis &scoliosis

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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Induction of fatigue using isometric neck flexor muscle endurance test (NET):
Time Frame: six months
a. An isometric neck muscle endurance test (NME test) will be performed for the deep neck flexors (Rectus Capitus Anterior, Rectus Capitus Lateralis, Longus Capitus, Longus Colli) until exhaustion in all participants occurs. with the subject in hook lying position through CHIN RETRACTION AND HEAD ELEVATED FROM THE COUCH.
six months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Measurement of neck proprioception using cervical joint position error test via OVERHEAD LASER POINTER
Time Frame: six months
: A laser pointer will be fixed to a headband or strap. Target paper will be typically 40 cm in diameter that contains concentric circles in 1 cm increments, divided into 4 quadrants intersecting at the zero.
six months

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Multi-Directional Reach Test
Time Frame: six months
Multi-Directional Reach (MDRT) is an inexpensive screening tool to determine the limits of stability of individuals in 4 directions. It measure how far an individual can voluntarily reach, thereby shifting the COG to the limits of the BOS with the feet stationary. The MDRT is a valid and reliable clinical measure for limits of stability. The test can be used to assess human postural stability in different four direction as follow (Roberta 2001)
six months
Biodex Balance System for The postural stability test
Time Frame: six months
The postural stability test emphasized on subject's ability to maintain center of balance. The subject's score on this test will assess the deviations from center, thus a lower score is more desirable than a higher score. Platform stability could be varied during this test by selecting (more options) from the Postural Stability Testing screen. It was proved that trial time, number of trials, starting and ending platform stability, rest count-downs or bilateral test could be set (Tropp and Odenrick., 2011).
six months

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 (Actual)

March 31, 2019

Primary Completion (Actual)

June 15, 2020

Study Completion (Anticipated)

July 20, 2020

Study Registration Dates

First Submitted

June 14, 2019

First Submitted That Met QC Criteria

June 24, 2019

First Posted (Actual)

June 26, 2019

Study Record Updates

Last Update Posted (Actual)

June 18, 2020

Last Update Submitted That Met QC Criteria

June 16, 2020

Last Verified

June 1, 2020

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • P. T. REC/012/002299

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

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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