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Effects of Eye-Movement Training Combined with Conventional Physical Therapy versus Conventional Physical Therapy Alone on Chronic Non-Specific Neck Pain: A Randomized Controlled Trial

Effects of Eye-Movement Training Combined with Conventional Physical Therapy versus Conventional Physical Therapy Alone on Chronic Non-Specific Neck Pain: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500111782
Enrollment
Unknown
Registered
2025-11-05
Start date
2025-12-01
Completion date
Unknown
Last updated
2025-11-11

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

Intervention group:Eye Movement Exercise combined with Conventional Physical Therapy

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: (1) Participants with non-specific neck pain **without radicular symptoms** (no clear precipitating factor, and exclusion of other specific cervical diseases such as cervical fracture, spinal tuberculosis, cervical tumor, or cervical disc herniation with evident nerve-root or spinal-cord compression). (2) Adults aged 18–60 years, either sex. (3) No history of autonomic-nerve-function training within the previous 6 months. (4) Pain intensity > 3 on the Visual Analogue Scale (VAS).

Exclusion criteria

Exclusion criteria: (1) Cognitive impairment or upper-motor-neuron lesions. (2) Conditions or medications known to alter heart-rate variability (daily use of analgesics, corticosteroids, ß-blockers, antidepressants, etc.). (3) Body-mass index > 30. (4) Severe cardiac or pulmonary disease, or any acute infectious disease. (5) Previous cervical-spine surgery. (6) Pain attributable to tumour, tuberculosis, fracture, or other specific pathology. (7) Pregnancy or unstable vital signs. (8) Chronic ocular disease. (9) Refusal to sign the informed-consent form.

Design outcomes

Primary

MeasureTime frame
Visual analog scale (VAS);

Secondary

MeasureTime frame
HRV test;Neck Disability Index(NDI) ;Cervical range of motion (ROM) measured by length;Anxiety (SAS) scale;Depression (SDS) scale;Electrical detection threshold;Electrical pain threshold;The eye blink and tracking accuracy;

Countries

China

Contacts

Public ContactLin Yang

West China Hospital, Sichuan University,China

green.yanglin@qq.com+86 177 0811 2611

Outcome results

None listed

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