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Clinical Observation of Physiological lodorsis Changes in Patients with Chronic Neck Pain Following Rehabilitation Treatment

Clinical Observation of Physiological lodorsis Changes in Patients with Chronic Neck Pain Following Rehabilitation Treatment

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500108149
Enrollment
Unknown
Registered
2025-08-26
Start date
2025-09-01
Completion date
Unknown
Last updated
2025-09-01

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

Conditions

Chronic Neck Pain

Interventions

Experimental group:A 4-week physiotherapy
Control group:None

Sponsors

The First Affiliated Hospital of Kunming Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged between 18 and 65 years old; 2. Regular daily life without history of special diseases; 3.180° (defined as physiological curvature straightening of the cervical spine) 5. Have the ability to communicate, understand, and give consent, and be able to follow the trial arrangements; 6. Good compliance and able to cooperate with post-training follow-up requirements.

Exclusion criteria

Exclusion criteria: 1. A history of cervical spine trauma or other musculoskeletal disorders is present; 2. There is ongoing use or administration of muscle-related medications; 3. The individual has implantable electronic devices (e.g., pacemakers) or experiences persistent instability in blood pressure and heart rate; 4. Patients exhibit a Visual Analogue Scale (VAS) score for neck pain exceeding 6 (Falla et al., 2007); 5. Patients diagnosed with cervical spondylotic myelopathy or cervical instability; 6. Patients lacking complete sagittal imaging data of the cervical spine or muscle function indices; 7. Patients suffering from infectious diseases or mental health disorders; 8. Women who are pregnant, breastfeeding, or planning to become pregnant; 9. Individuals who have participated in other clinical studies within the past four weeks; 10. Cases where the investigator deems the individual unsuitable for participation in the study.

Design outcomes

Primary

MeasureTime frame
Cobb angle of neck;

Countries

China

Contacts

Public ContactDing Tao

The First Affiliated Hospital of Kunming Medical University

dt101180@sina.com+86 136 1871 3969

Outcome results

None listed

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