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Neuroimaging study on the effect of acupuncture on pain perception brain network in patients with chronic neck pain

The study on the central mechanism of acupuncture effect in patients with chronic pain

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800017718
Enrollment
Unknown
Registered
2018-08-10
Start date
2018-08-01
Completion date
Unknown
Last updated
2018-08-20

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

Conditions

Chronic Neck Pain

Interventions

Individualized acupuncture group:acupuncture on the sensitized points

Sponsors

the Teaching Hospital of Chengdu University of TCM
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Complaints of neck pain /discomfort, stiffness or limited cervical activity; (2) Aged 18 to 75 years old, male or female, right-handedness; (3) For 5 days out of every 7 days, the neck pain/discomfort score estimated by visual analogue scale (VAS) was more than 3; (4) The course of neck pain continue more than 3 months; (5) In this study, the volunteer with good compliance, willing to cooperate with the research, voluntarily join in this study and sign the informed consent of patients. noted: patients who meet the above 5 items may be included in this study

Exclusion criteria

Exclusion criteria: (1) Under 18 years old or over 75 years old; (2) In the past three months, cervical spondylosis has been treated with acupuncture or medicine; (3) Patient who have cervical vertebral tuberculosis, tumor, spinal canal occupying lesions and scoliosis; (4) 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; (5) Severe osteoporosis and cardiovascular and cerebrovascular diseases, digestive, urinary, blood, endocrine system and other serious diseases or clinical control is not up to standard; (6) The history of alcoholism or drug abuse habits; (7) The pregnant and lactating women, and have fertility requirements women in the following six months; (8) Who were participating in other clinical studies. Note: all patients who meet any of the above shall be excluded

Design outcomes

Primary

MeasureTime frame
Visual Analogue Score(VAS);

Secondary

MeasureTime frame
Northwick Park Questionnaire (NPQ); short-form of McGill pain questionnaire;Neck Disability Index (NDI);Short-form 12-Item Health Survey (SF-12);Self-Rating Anxiety Scale(SAS);Self-Rating Depression Scale(SDS);cervical range of motion (CROM);

Countries

China

Contacts

Public ContactZhao ling

Acupuncture and Tuina School, 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