NCT07230938

Brief Summary

This observational cross-sectional study aims to investigate the impact of cervical proprioception deficits on postural stability in patients with cervical spondylosis. Using pedobarographic analysis, the study will assess static balance parameters in affected individuals. The main question it aims to answer is: Does Cervical proprioception deficits affect postural stability in patients with cervical spondylosis measured by pedobarographic parameters?

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
82

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Nov 2025

Shorter than P25 for all trials

Status
not yet recruiting

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

September 22, 2025

Completed
2 months until next milestone

Study Start

First participant enrolled

November 15, 2025

Completed
2 days until next milestone

First Posted

Study publicly available on registry

November 17, 2025

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 30, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 30, 2025

Completed
Last Updated

November 17, 2025

Status Verified

October 1, 2025

Enrollment Period

2 months

First QC Date

September 22, 2025

Last Update Submit

November 13, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Postural stability measured using a foot pressure platform

    Postural stability will be assessed by measuring postural sway using a force platform (stabilometer) under two conditions (eyes open and eyes closed). The primary variable will be the ellipse surface area (mm²) representing the center of pressure sway.

    Single assessment at baseline (Day 1)

Secondary Outcomes (1)

  • Cervical joint position error (JPE) measured using overhead laser pointer

    Single assessment at baseline (Day 1)

Interventions

Pedobarography system (foot pressure plateform) for Postural Stability assessment will be used to assess Postural stability. the pedobarographic analysis will be delivered using the FreeMed Professional platform (Sensor Medica, Rome, Italy). It evaluates the distribution of foot pressure on the ground.Three components make up the platform: a central mat with resistance sensors and two passive mats at either end that form a walking path. The platform is connected to a computer, to which all data is displayed and processed using FreeStep software

Also known as: FREEMED baropodometric platform and FREESTEP software -v.2.01.054

laser pointer for Cervical proprioception device will be used to assess cervical proprioception by preforming Cervical joint position error (JPE) test

Eligibility Criteria

Age25 Years - 50 Years
Sexall
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
Study Population

Eighty-two patients with cervical spondylosis will represent the sample of this study. They will be selected from the outpatient clinic of Faculty of Physical Therapy, Delta University. All the patients will sign a consent form before starting the study

You may qualify if:

  • Eighty-two patients with cervical spondylosis, the patient will be diagnosed and referred by physician.
  • Mild to moderate cervical disability according to neck disability index( MacDermid et al., 2009).
  • Age ranges from 25 to 45 years.
  • Body mass index from 18.5 - 24.9.

You may not qualify if:

  • The patients will be excluded if they have one of the following:
  • visual or vestibular sensory disorders or cerebellar disease.
  • Cervical myelopathy.
  • Patients with previous cervical surgery.
  • inflammatory diseases involving cervical spine such as rheumatoid arthritis or ankylosing spondylitis.
  • History of cervical trauma including whiplash associated disorders (WAD).
  • History of cervical tumors.
  • History of ankle instability.
  • No previous foot and ankle surgery.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Central Study Contacts

AISHA MOURAD MOHAMMED, Bachelor of physical therapy

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
principal investigator, MSc candidate

Study Record Dates

First Submitted

September 22, 2025

First Posted

November 17, 2025

Study Start

November 15, 2025

Primary Completion

December 30, 2025

Study Completion

December 30, 2025

Last Updated

November 17, 2025

Record last verified: 2025-10