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A Clinical Study on the Improvement of Lateral Flexion Function and Emotional Disorders in Patients with Chronic Neck Pain through Tuina Based on the Sinew Theory

A Clinical Study on the Improvement of Lateral Flexion Function and Emotional Disorders in Patients with Chronic Neck Pain through Tuina Based on Meridian Theory.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026001210
Enrollment
Unknown
Registered
2026-05-07
Start date
2026-06-05
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Chronic neck pain

Interventions

Control Group:Routine local manipulation of the neck
Intervention Group:Foot Shaoyang Sinew Distal Manipulation

Sponsors

The Second Affiliated Hospital of Hunan University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: (1) Meets the above diagnostic criteria; (2) Age between 20-60 years, gender; (3) Visual Analog Scale (VAS) score =3 cm, accompanied by cervical lateral flexion dysfunction; (4) Negative affect score in the Positive and Negative Affect Schedule (PANAS) =15 points, or Patient Health Questionnaire (PHQ-9) depression scale =5 points; (5) Clear consciousness, able to correctly understand and cooperate, and capable of clear expression; (6) Voluntarily participates in this study and signs the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Those with a history of cervical trauma, cervical surgery, or tumor; (2) Patients with severe diseases of the heart, brain, kidneys, liver, or other vital organs, or abnormal mental behavior that makes cooperation impossible; (3) Patients with exacerbation of pre-existing internal medical conditions or sudden cerebrocardiovascular diseases who are unsuitable for continued acupuncture treatment; (4) Patients who have participated in other clinical trial projects within 14 days prior to this study; (5) Patients with cognitive or communication impairments who are unable to cooperate with treatment or follow-up.

Design outcomes

Primary

MeasureTime frame
Cervical Range of Motion (CROM);Visual Analog Scale;Positive and Negative Affect Schedule;

Secondary

MeasureTime frame
Pittsburgh sleep quality index;Patient Health Questionnaire-9;

Countries

China

Contacts

Public ContactZhan Deng Jie

The Second Affiliated Hospital of Hunan University of Traditional Chinese Medicine

2942265416@qq.com18773569827

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Jun 11, 2026