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Investigating the Long-Term Efficacy and Neural Mechanisms of Sensorimotor Training in Patients with Chronic Non-Specific Neck Pain

The Efficacy of Sensorimotor Training and Its Brain Network Mechanisms in Patients with Chronic Nonspecific Neck Pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500110259
Enrollment
Unknown
Registered
2025-10-11
Start date
2025-10-11
Completion date
Unknown
Last updated
2025-10-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Non-Specific Neck Pain

Interventions

Sensory-Motor Training Group:Sensory-motor online intervention, 3 times per week, 40 minutes per session, for a total of 12 weeks.
Standard Exercise Group:Conventional exercise online intervention, 3 times per week, 40 minutes per session, for a total of 12 weeks.

Sponsors

Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. Diagnosed with chronic nonspecific neck pain, defined as chronic pain in the anatomical region of the cervical spine and its surrounding musculature, excluding disc disease, rheumatic conditions, or cervical tumors; 2. Recurrent neck discomfort lasting more than 3 months; 3. Neck pain NRS score between 3 and 8 (inclusive) within the past 7 days or at the most recent episode; 4. Age between 18 and 45 years; 5. No acute neck pain or chronic/acute pain in other body regions prior to testing; 6. No use of opioid analgesics, hypnotics, or anxiolytic/antidepressant medications within one month before testing; 7. Voluntary participation in the trial with signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Presence of symptoms or signs of nerve root compression; 2. History of neck trauma or surgery; 3. Spinal cord lesions or congenital spinal cord disorders; 4. Cervical tumors or tuberculosis; 5. Rheumatic diseases of the neck and shoulders; 6. Sensory aphasia, cognitive impairment, or severe visual/hearing impairment that interferes with assessment; 7. Concurrent severe conditions such as cardiac disease, liver disease, hematologic disorders, or malignancies; 8. Pregnant or lactating women; 9. Patients currently receiving other treatments for chronic nonspecific neck pain, or who received such treatment within the past 6 months.

Design outcomes

Primary

MeasureTime frame
Visual Analog Scale;Neck Disability Index;Northwick Park Neck Pain Questionnaire;

Secondary

MeasureTime frame
Heat Pain Threshold;Pressure Pain Threshold;Joint Position Error;Active Range of Motion;Cervical Maximum Isometric Muscle Strength;Cranio-Cervical Flexion Test;Pittsburgh Sleep Quality Index (PSQI);Anxiety Status;Depression Status;Fear-Avoidance Beliefs Questionnaire (FABQ);Pain Catastrophizing;Fear of Movement;STarT Back Risk Screening Tool;

Countries

China

Contacts

Public ContactBai Yiwen

Shanghai University of Traditional Chinese Medicine

baiyiwen0507@163.com+86 51323199

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026