Skip to content

Study on the Early Warning and Treatment of Cervical Spondylosis of Cervical Type on Young People Based on the Move Generate Yang Theory

Study on the Early Warning and Treatment of Cervical Spondylosis of Cervical Type on Young People Based on the Move Generate Yang Theory

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02199405
Enrollment
140
Registered
2014-07-24
Start date
2014-09-30
Completion date
Unknown
Last updated
2014-09-03

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

Conditions

Cervical Spondylosis of Cervical Type

Keywords

Spondylosis, Massage Therapy, Exercise Therapy ,Treatment Efficacy

Brief summary

The incidence of cervical spondylosis on young people is increasing every year. Suffering from this disease will affect the normal life and learning of young people. Episode younger and incidence higher of this disease could increase health care spending of the government in the economy. Cervical spondylosis of cervical type is the main type of cervical spondylosis of young people. Patients of cervical spondylosis of cervical type always manifest the head, neck and shoulder pain accompanied by corresponding pressure point, the X-ray display of Upper cervical curvature change and instability of intervertebral joint performance ,and the dynamic lateral X-ray shows vertebral instability or trapezoidal change. The conservative treatment is the primary and preferred treatment of the disease. This study is designed as a random, control, single blind study. It will recruit 140 cases of cervical spondylosis of cervical type. Both the treatment group and the control group will be randomly assigned 70 cases. Patients in the treatment group will be treated by Massage of chiropractic and adjusting cervical curvature and practice Sishi Daoyin for 4 weeks,and the control group by conventional massage and cervical traction. The total study includes 2 views that are baseline and post-4week intervention. At all of the 2 views, all participants will be examined range of motion of cervical vertebra, cervical curvature, and Surface Electromyography of neck muscles, and will be estimated scores of The Neck Disability Index(NDI), the Northwick Park Neck Pain Questionnaire (NPQ),Short-form McGill Pain Questionnaire(SF-MPQ) and Evaluation of the therapeutic effect. This study aims to investigate the efficacy of Massage of chiropractic and adjusting cervical curvature and Sishi Daoyin practice, and discover the correlation between these scales and these objective indicators to discover the indicators of early warning signs of cervical spondylosis of cervical type of young people.

Detailed description

Quality control: The study site and all researchers must comply with the required qualifications. All researchers must be trained before the study. The study will take a number of measures to ensure the recruitment of the required sample size, and compliance of intervention providers and participants.

Interventions

OTHERMassage of chiropractic and adjusting cervical curvature

Massage of chiropractic and adjusting cervical curvature, 10 minutes, three times one week for 4 weeks

OTHERSishi Daoyin

Sishi Daoyin, practicing during 9-11am, once a day for 4 weeks

Conventional massage , 15 minutes, three times one week for 4 weeks

Sponsors

Wang Yucheng
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
15 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* meet the diagnostic criteria of cervical spondylosis of cervical type * first invasion and not receive any treatment * X-ray shows cervical curvature go straight * volunteered to join the test, and sign informed consent persons

Exclusion criteria

* suspected or confirmed bone and joint and soft tissue tumors, and so on * suffer from cardiovascular, lung, liver, kidney and hematopoietic system serious illness or impairment * lesions of skin ( such as damage, burns, and so on ) where massage will be applied * severe congenital malformation of cervical vertebra * incapacitated or unable to independently read and write * other conditions which researchers consider appropriate to participate in this study

Design outcomes

Primary

MeasureTime frameDescription
value of cervical curvaturebaseline and post- 4week interventionWe will examine the value of cervical curvature of participants at baseline and post- 4week intervention.

Secondary

MeasureTime frameDescription
range of motion of cervical vertebrabaseline and post- 4week interventionWe will examine the range of motion of cervical vertebra, including cervical flexion, extension, flexion to the left, flexion to the right, rotation to the left and rotation to the right.
value of Surface Electromyography of neck musclesbaseline and post- 4week interventionWe will examine the value of Surface Electromyography of sternocleidomastoid muscle and upper trapezius muscle when they are cervical flexion, extension, flexion to the left and flexion to the right.
scores of the Northwick Park Neck Pain Questionnaire (NPQ)baseline and post- 4week interventionWe will estimate the scores of NPQ of participants.
scores of Short-form McGill Pain Questionnaire(SF-MPQ)baseline and post- 4week interventionWe will estimate the scores of SF-MPQ of participants.
scores of the Neck Disability Index(NDI)baseline and post- 4week interventionWe will estimate the scores of NDI of participants.

Other

MeasureTime frameDescription
degree of Evaluation of the therapeutic effectbaseline and post- 4week interventionWe will estimate the degree of Evaluation of the therapeutic effect according to Standards of the diagnosis and the therapeutic effect of Disease and Syndrome of traditional Chinese medicine.

Countries

China

Contacts

Primary ContactJennifer Gao, Master
jennifergao1982@126.com022-27432929
Backup ContactJames Zhang, Master
james399@126.com022-27432929

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026