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A Study of the regressive mechanism of pain memory with electro-acupuncture intervention based on 'acupuncture at pain points' theory

A Study of the regressive mechanism of pain memory with electro-acupuncture intervention based on 'acupuncture at pain points' theory

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IIR-17010797
Enrollment
Unknown
Registered
2017-01-22
Start date
2017-03-28
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Cervical spondylosis (Chronic neck pain)

Interventions

1:Sensitized acupuncture
2:conventional acupuncture

Sponsors

the Teaching Hospital of Chengdu University of TCM
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Suffering from neck pain and stiffness; 2. Meet the diagnostic criteria of cervicalspondylotic radiculopathy or cervical spondylosis of nerve root type; 3. aged 18 to 65 years old, male or female, right-handed; 4. The neck pain and discomfort continue more than 3 months; 5. Cervical pain / discomfort was estimate by visual analogue scale (VAS) score of greater than 3 scors; 6. In this study, the volunteer voluntarily join in this study and signed the informed consent of patients. Note: patients who meet the above 6 items may be included in this study

Exclusion criteria

Exclusion criteria: 1. In the past three months, cervical spondylosis has been treated with acupuncture or medicine; 2. Patient who have Cervical vertebral tuberculosis, tumor, spinal canal occupying lesions and scoliosis; 3. The cervical lesions (thoracic outlet syndrome, tennis elbow, carpal tunnel syndrome, cubital tunnel syndrome, periarthritis of shoulder, biceps tenosynovitis etc.) caused by the above reason of leg pain; 4. Severe osteoporosis and cardiovascular and cerebrovascular diseases, digestive, urinary, blood, endocrine system and other serious diseases or clinical control is not up to standard; 5. The history of fainting of needle or alcoholism or drug abuse habits; 6. The pregnant and lactating women, and have fertility requirements women in the following six months; 7. Who were participating in other clinical studies. Note: all patients who meet any of the above shall be excluded

Design outcomes

Primary

MeasureTime frame
Northwick Park Questionnaire;

Secondary

MeasureTime frame
Neck Disabilitv Index (NDI);Stroop Effect;short-form of McGill pain questionnaire;Beck Anxiety Inventory(BAI);Beck Depression Inventory(BDI);the MOS 12-item Short Form Health Survey (SF-12);

Countries

China

Contacts

Public ContactZhao ling

Chengdu university of Traditional Chinese Medicine

ling94@163.com+86 13568801429

Outcome results

None listed

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