The Effects of Cervical Sensorimotor Control Challenges on Gait Patterns, Cervical Sensorimotor Control During Dynamic Tasks
Influence of Various Cervical Sensorimotor Control Challenges on Gait Patterns, Cervical Sensorimotor Control, and Dual-Task Performance During Dynamic Gait-related Tasks
1 other identifier
observational
60
1 country
1
Brief Summary
To investigate the influence of cervical SMC challenges during gait-related dynamic tasks on all task performance and symptoms in patients with CNP.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Dec 2024
1 active site
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
June 19, 2024
CompletedFirst Posted
Study publicly available on registry
August 7, 2024
CompletedStudy Start
First participant enrolled
December 16, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 30, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2025
CompletedApril 8, 2026
April 1, 2026
10 months
June 19, 2024
April 7, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (14)
Spatiotemporal parameter
Gait speed (meter/second)
One day
Spatiotemporal parameter
cadence (steps/minute)
One day
Spatiotemporal parameter
stride length (meter)
One day
Spatiotemporal parameter
stride duration (second)
One day
Spatiotemporal parameter
stance duration (second)
One day
Spatiotemporal parameter
swing duration (second)
One day
Spatiotemporal parameter
stance length (meter)
One day
Spatiotemporal parameter
swing length (meter)
One day
Spatiotemporal parameter
step width (meter)
One day
Head and Cervical Kinematics
Mean, range, maximum, and minimum of the angular displacements (degree)
One day
Head and Cervical Kinematics
Mean and peak angular velocity (m/s) and acceleration (m/\^2)
One day
Lower Extremity Kinematics and Kinetics
Maximum, minimum, and range angular displacement (degree of joint angle)
One day
Lower Extremity Kinematics and Kinetics
Mean and peak angular velocity and acceleration (m/\^2)
One day
Enter of Mass and Center of Pressure (COM-COP)
A 15-component link-segment model will be used to estimate the location of the total body COM. The center of pressure (COP) data will be derived from the outputs of the AMTI force platform.
One day
Study Arms (2)
Idiopathic neck pain group
Pain was unilateral or bilateral between the superior nuchal line and 1st thoracic vertebra; Neck pain persisting for 3 months and above; Average pain intensity of last pain episode was between 2 and 8 based on the numerical rating scale (NRS).
Asymptomatic adult group
Do not have any complaints of current pain and impairments of neuromusculoskeletal systems within the last 6 months.
Eligibility Criteria
Patients with chronic neck pain are: (1) pain was unilateral or bilateral between the superior nuchal line and 1st thoracic vertebra, (2) neck pain persisting for 3 months and above, and (3) average pain intensity of last pain episode was between 2 and 8 based on the numeric rating scale (NRS).
You may qualify if:
- Healthy asymptomatic adults will not have any complaints of current pain and impairments of neuromusculoskeletal systems within the last 6 months.
- For patients with CNP
- Pain was unilateral or bilateral between the superior nuchal line and 1st thoracic vertebra
- Neck pain persisting for 3 months and above
- Average pain intensity of last pain episode was between 2 and 8 based on the numeric rating scale (NRS).
You may not qualify if:
- ◾For patients with CNP and healthy asymptomatic adults
- Acute or the first onset of neck pain
- Traumatic cause of pain
- Previous fracture or surgery of the spine
- Diagnosed cardiopulmonary diseases, for example, chronic obstructive pulmonary disease, pulmonary tuberculosis, asthma, chronic bronchitis, pulmonary emphysema
- Diagnosed gastrointestinal and abdominal conditions which may interfere daily activities within the past 6 months
- Medical conditions that may affect balance and study procedures (e.g. neurological diseases, vestibular disorders, malignant tumors)
- Metabolic diseases such as anemia and diabetes
- Smoking, plan to pregnant or in pregnancy
- Psychological disorders (affect questionnaire responses)
- Unable to walk independently
- Corrected visual abnormalities or individuals unable to wear contact lenses for vision correction due to the potential interference of wearing VR head-mounted display with glasses.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
National Cheng Kung University
Tainan, Taiwan, 701, Taiwan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- professor
Study Record Dates
First Submitted
June 19, 2024
First Posted
August 7, 2024
Study Start
December 16, 2024
Primary Completion
September 30, 2025
Study Completion
December 31, 2025
Last Updated
April 8, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will not share