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Clinical Trials/NCT05032911
NCT05032911
Unknown
Not Applicable

Analysis of Sensorimotor Control in People With and Without Neck Pain Using Inertial Sensor Technology: Study Protocol for a Longitudinal Prospective Observational Study

CEU San Pablo University0 sites100 target enrollmentOctober 10, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Movement Disorders
Sponsor
CEU San Pablo University
Enrollment
100
Primary Endpoint
Smoothness of motion
Last Updated
4 years ago

Overview

Brief Summary

This is a descriptive, observational, longitudinal, prospective study consecutively enrolling patients with non-specific neck pain and age-matched asymptomatic participants.

The investigators will register sensorimotor control variables, including active range of motion, movement speed, acceleration, smoothness of motion, head repositioning accuracy and motion coupling patterns. These variables will be recorded by means of Inertial Measurement Unit (IMU) sensors during the following tests consecutively performed in two measuring sessions separated by 12 months: (a) kinematics of planar movements, (b) kinematics of the craniocervical flexion movement, (c) kinematics during functional tasks and (d) kinematics of task-oriented neck movements in response to visual targets.

Registry
clinicaltrials.gov
Start Date
October 10, 2021
End Date
February 15, 2023
Last Updated
4 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
CEU San Pablo University
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Population aged between 18 and 65 years old

Exclusion Criteria

  • Visual impairment not corrected by the use of glasses/contact lenses
  • Migraine headache
  • Complex regional syndrome
  • Previous surgeries in the neck and/or head region
  • Sensory and/or vestibular alterations, (f) Otogenic or idiopathic vertigo/dizziness
  • Presence of tumors in the craniocervical region
  • Previous fracture in the head or neck region
  • Osseous deformities in the thoracic, cervical or cranial region

Outcomes

Primary Outcomes

Smoothness of motion

Time Frame: 1 year

expressed as movement jerk (º/sec3)

Head repositioning accuracy

Time Frame: 1 year

Calculated as the repositioning error considering the difference between the neutral starting position and the following positions reached after the performance of any of the movements

Motion coupling patterns

Time Frame: 1 year

Calculated as the angular displacement occurring in a different anatomical plane to the one that is being tested for each of the planar movements

Active range of motion

Time Frame: 1 year

Expressed as an angular displacement (°) in 3 full-movements (flexion-extension, lateral flexion and rotation)

Movement speed

Time Frame: 1 year

Expressed as angular velocity (°/sec) in 3 full-movements (flexion-extension, lateral flexion and rotation)

Secondary Outcomes

  • Pain-related fear-avoidance(1 year)
  • Physical activity level(1 year)
  • Fear of movement and injury(1 year)

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