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Cervical spondylosis treated by Stretching-Relaxation-Adjustment Manipulation(SRAM): a randomized controlled trial

Cervical spondylosis treated by Stretching-Relaxation-Adjustment Manipulation(SRAM): a randomized controlled trial

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100051003
Enrollment
Unknown
Registered
2021-09-10
Start date
2021-09-20
Completion date
Unknown
Last updated
2022-05-16

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

Conditions

Cervical spondylosis

Interventions

Group 1:Stretching-Relaxation-Adjustment Manipulation(SRAM)
Group 2:conventional tuina

Sponsors

The First Affiliated Hospital, Yunnan University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria, neck pain, with or without back pain or soreness and limited neck movement; 2. Age 18-70 years old, male or female; 3. Those who have not received treatment in the past 2 weeks; 4. The person who signed the informed consent form himself or his immediate family.

Exclusion criteria

Exclusion criteria: 1. Cervical vertebral body tuberculosis, tumors, etc. with vertebral body destruction or space-occupying lesions in the spinal canal and scoliosis; 2. Those who have been diagnosed with cervical spondylosis but have undergone surgery; 3. Headache caused by intracranial organic lesions and diseases, such as intracranial infection, brain tumor, subarachnoid hemorrhage, etc.; 4. Patients with serious primary diseases of the heart, brain, blood vessels, kidneys, liver, digestion, hematopoietic disorders, diabetes and other organs or systems; 5. Pregnant women, lactating women and women who have childbearing requirements in the past six months; 6. Those who cannot understand or record relevant scoring indicators; 7. Persons with mental retardation, moderate or higher anxiety, depression and other mental illnesses; 8. Those who are seriously afraid of acupuncture and cannot cooperate with acupuncture; 9. Those who are engaged in other pain medicines or physical therapy, or who are participating in other clinical trials.

Design outcomes

Primary

MeasureTime frame
PainVision perceptive pain quantitative(VAS,PD,PR);

Secondary

MeasureTime frame
Reform of Northwick Park Neck Pain Questionnaire (NPQ);Self-rating Anxiety Scale(SAS);Self-rating Depression Scale(SDS);

Countries

China

Contacts

Public ContactDong Youkang

The First Affiliated Hospital, Yunnan University of Chinese Medicine

dykheaven@126.com+86 13529396660

Outcome results

None listed

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