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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
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2100005289
Enrollment
Unknown
Registered
2021-09-10
Start date
2021-09-20
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

Cervical spondylosis

Interventions

the conventional Tuina group:Manipulation
Stretching-Relaxation-Adjustment Manipulation(SRAM) group:Manipulation

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)cervical spondylosis originated from neck pain with or without back pain or soreness, limited movement of the neck, by Guide for diagnosis, treatment and rehabilitation of cervical spondylosis Chinese Association of Rehabilitation Medicine in 2016; (2) Aged 18-70 years male and female; (3) No treatment within 2 weeks; (4) Who sign or direct relatives to sign informed consent.

Exclusion criteria

Exclusion criteria: (1) Patient who have Cervical vertebral tuberculosis, tumor, spinal canal occupying lesions and scoliosis; (2) Patient who had operated after being confirmed with cervical spondylosis; (3) Headache result from intracranial diseases, such as intracranial infection, cerebroma, subarachnoid hemorrhage and other diseases; (4) Patients with serious primary diseases of the heart, brain, blood vessels, kidneys, liver, digestive, hematopoietic disorders, diabetes, etc.; (5) Women who have fertility requirements during pregnancy, lactation and nearly half a year; (6) Failing to understand or record the relevant scoring indicators; (7) Mentally ill persons with mental retardation, moderate or higher levels of anxiety and depression; (8) Unable to cooperate with the acupuncture; (9) Who is involved in other pain medications or physical therapists, or are participating in other clinical trials.

Design outcomes

Primary

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

Secondary

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

Countries

China

Contacts

Public ContactDong Youkang

The First Affiliated Hospital, Yunnan University of Chinese Medicine

dykheaven@126.com13529396660

Outcome results

None listed

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