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
42 participants
OBSERVATIONAL
2025-06-01
2025-11-01
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 Neuroscience-Based Exercise
NCT05788263
The Effects of Cervical Sensorimotor Control Challenges on Gait Patterns, Cervical Sensorimotor Control During Dynamic Tasks
NCT06542302
Relationship of Deep Cervical Flexor Muscle Endurance With Neck Position Sense and Body Balance
NCT03489954
Evaluation of Cervical Position and Movement Sense Using a Novel Computer Vision-Based Software
NCT07181798
Effect of Stabilization Exercises in Individuals With Non-Specific Chronic Neck Pain.
NCT05369260
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Single-task walking (walking at a self-selected pace), Motor dual-task walking (walking while carrying a tray with a glass of water), and Cognitive dual-task walking (walking while verbally reporting the number of letters in presented words).
Gait parameters will be measured using the BTS G-Walk wearable sensor system, which records accelerometric data at the lumbar level (L4-L5) and calculates temporospatial parameters. Gait variability will be quantified using the coefficient of variation formula, and gait symmetry will be determined using symmetry index calculations.
The primary outcomes are gait variability and gait symmetry across the three walking conditions. Secondary outcomes include pain characteristics, the Neck Disability Index (NDI), and the Bournemouth Neck Questionnaire (BNQ).
The study hypothesizes that both motor and cognitive dual-task conditions will significantly affect gait variability and symmetry in individuals with NSNP, and these effects will differ from those observed in healthy controls. Findings are expected to improve understanding of motor control alterations in NSNP and provide guidance for individualized rehabilitation programs and therapeutic interventions.
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
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Nonspecific Neck Pain
Adults aged 18-60 with chronic nonspecific neck pain (≥3 months), scoring ≥10 on the Neck Disability Index, no neurological/systemic disease, no prior cervical surgery.
No interventions assigned to this group
Healthy Control
Age- and sex-matched adults without neck pain or neurological/systemic disorders.
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
* Adults aged 18-60 years
* History of nonspecific neck pain lasting at least 3 months
* Neck Disability Index (NDI) score ≥10
* Willingness to participate and provide informed consent
* for the Healthy Control group
* Adults aged 18-60 years
* No history of neck pain or musculoskeletal/neurological/systemic disorders
* Willingness to participate and provide informed consent
Exclusion Criteria
* History of traumatic cervical injury
* Diagnosed cervical radiculopathy, spondylosis, spondylolisthesis, or disc herniation
* Presence of any neurological or systemic disease
* Musculoskeletal disorders affecting gait performance
* Cognitive impairment or psychiatric conditions interfering with test participation
18 Years
60 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Yuksek Ihtisas University
OTHER
Hacettepe University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Güngör Beyza ÖZVAR
Principal Investıgator
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Busra Kalkan Balak
Role: PRINCIPAL_INVESTIGATOR
Yuksek Ihtisas University
Elıf Sena Colak
Role: PRINCIPAL_INVESTIGATOR
Yuksek Ihtisas University
Aslı Isıkdemır
Role: PRINCIPAL_INVESTIGATOR
Yuksek Ihtisas University
Demet Cıhan
Role: PRINCIPAL_INVESTIGATOR
Yuksek Ihtisas University
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Yuksek Ihtisas University
Ankara, , Turkey (Türkiye)
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.
non-spesific neck pain
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.