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Clinical study of the immediate efficacy of acupuncture combined with active exercise in the rapid treatment for pain and movement disorders in patients with acute stiff neck

Clinical study of the immediate efficacy of acupuncture combined with active exercise in the rapid treatment for pain and movement disorders in patients with acute stiff neck

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200066997
Enrollment
Unknown
Registered
2022-12-23
Start date
2023-01-01
Completion date
Unknown
Last updated
2024-05-21

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

Conditions

Acute stiff neck

Interventions

Group A:acupuncture combined with active exercise
Group B:sham acupuncture combined with active exercise
Group C:active exercise

Sponsors

Second Affiliated Hospital of Yunnan University of Chinese Medicine/ School of Acupuncture and Massage-Rehabilitation/The Second Affiliated Hospital, Yunnan University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: (1) Meet the diagnostic criteria for stiff neck and are in the acute phase; (2) Aged between 18 and 60 years old; (3) 4 =VAS score =9; (4) Volunteering to participate in the study and signing informed consent. (Note: Patients who meet the above 4 items at the same time may be included in this study.)

Exclusion criteria

Exclusion criteria: (1) Patients with disease onset of more than seven days, according to the International Association for the Study of Pain; (2) Patients with cervical spine fracture, dislocation, tuberculosis, or tumor; (3) Patients with severe cardiovascular and cerebrovascular diseases; (4) Pregnant women or patients with skin allergies; (5) Patients with a history of syncope and unable to accept acupuncture treatment; (6) Unconsciousness, inability to express subjective discomfort symptoms and mental illness; (7) Severe local lesions (such as infection, burn, and scald) cannot be treated with acupuncture; (8) Patients who had received analgesic treatment; (9) Patients who are intolerant or uncooperative to exercise therapy. (Note: Patients meeting any of the above criteria will be excluded)

Design outcomes

Primary

MeasureTime frame
effective rate at 10 minutes of treatment;

Secondary

MeasureTime frame
effective rate at 0,0-1,2, 4, 6, 8, min;Visual analog scale score (VAS);Cervical range of motion evaluation sheet;

Countries

China

Contacts

Public ContactGuo Taipin

Yunnan University of Chinese Medicine/ Second Affiliated Hospital of Yunnan University of Chinese Medicine

gtphncs@126.com+86 184 8727 2658

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 6, 2026