Assessing Cervical Sensorimotor Control With VR in Chronic Neck Pain
NCT ID: NCT06474130
Last Updated: 2025-03-24
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
RECRUITING
80 participants
OBSERVATIONAL
2025-02-17
2027-07-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
The Effects of Cervical Sensorimotor Control Challenges on Gait Patterns, Cervical Sensorimotor Control During Dynamic Tasks
NCT06542302
Innovative Rehabilitation: Integrating VR-Based Sensorimotor Training Into Comprehensive Neck Rehabilitation
NCT06750718
Sensorimotor Dysfunction of Individuals With Neck Pain
NCT00174148
Virtual Reality and Cervical Mobilization
NCT05829564
Virtual Reality Application for Assessing Neck Movement and Position Sense
NCT07190014
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_CONTROL
CROSS_SECTIONAL
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Chronic 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).
No interventions assigned to this group
Healthy adults group
Do not have any complaints of current pain and impairments of neuromusculoskeletal systems within the last 6 months.
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* 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)
2. Healthy asymptomatic adults:
* Do not have any complaints of current pain and impairments of neuromusculoskeletal systems within the last 6 months
Exclusion Criteria
* 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
18 Years
60 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
National Science and Technology Council
FED
National Cheng Kung University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
YI-JU TSAI
professor
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
National Cheng Kung University
Tainan City, , Taiwan
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
NCKU_VR
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.