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Clinical study on the treatment of Neck Type Cervical Spondylosis with the "Yang's" acupuncture

Clinical study on the treatment of Neck Type Cervical Spondylosis with the "Yang's" acupuncture

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400081734
Enrollment
Unknown
Registered
2024-03-11
Start date
2023-04-19
Completion date
Unknown
Last updated
2024-03-18

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

Conditions

Neck Type Cervical Spondylosis

Interventions

Test group:Health promotion + "Yang's" acupuncture treatment Selected points are as follows: Ahshi point, cervical spine point, Xinshi, Tianzhu, Fengchi, Fengmen, Liejiao, and Nianjian. Method of oper
Control group:Health education + conventional acupuncture treatment Selected points are as follows: cervical spine point, Tianzhu, Houxi, Shenwei, Hangzhong. Methods of operation: conventional acupunc

Sponsors

Yueyang Hospital of Integrative Medicine, Shanghai University of Traditional Chinese Medicine, China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria for cervical cervical spondylosis in Chinese and Western medicine; 2. Age =20 years and =65 years, gender is not limited; 3. not taking painkillers within 1 month of entering this trial; 4. Voluntarily join this trial and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Combination of other disease causes of neck discomfort; 2. Those whose local skin is broken or swollen and not suitable for acupuncture treatment; 3. those who suffer from other serious diseases, such as tumor, tuberculosis, ankylosing spondylitis, combined with serious cardiac, cerebrovascular and other serious life-threatening primary diseases and patients with mental illness and cognitive dysfunction; 4. Women in pregnancy and lactation; 5. patients who have participated or are participating in other clinical trial studies within 1 month prior to enrollment.

Design outcomes

Primary

MeasureTime frame
(Northwick Park Neck Pain Questionnaire;

Secondary

MeasureTime frame
Neck Disabilition Index;The short-form 36 item health surveyquestionnaire;Self-rating Anxiety Scale;

Countries

China

Contacts

Public ContactQi Rui

Yueyang Hospital of Integrative Medicine, Shanghai University of Traditional Chinese Medicine, China

qirui36@126.com+86 189 3056 6807

Outcome results

None listed

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