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Preventive Care of Chronic Cervical Pain and Disabilities

CompletedNot applicableNCT00566930
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

Brief summary (from the registry)

The aim of this study is to determine which of tertiary prevention spinal manipulative therapy (SMT) or a home exercise program is the more efficient approach to reduce pain and increase functional capacity, quality of life and general health condition. To do so, 60 participants with chronic cervical pain, will be recruited and divided into 3 groups according to the intervention they will receive: control group, experimental group 1 who will receive preventive chiropractic care in the form of spinal manipulations and experimental group 2 will have to perform an individualized home exercise program on a daily basis. We hypothesize that a group of patient receiving SMT + a home exercise program will present less pain and functional disabilities over a 1 year period. The innovative value of this project is mainly related to the fact that it will generate new and potentially very useful data concerning the clinical significance of preventive chiropractic care. Moreover, such data will be beneficial to our profession as chiropractic makes a step towards prevention, wellness and public health.

Study details

Official title
Preventive Care of Chronic Cervical Pain and Disabilities; Comparison of Spinal Manipulative Therapy and Individualized Home Exercise Programs
Conditions
Interventions
Sponsor
Université du Québec à Trois-Rivières
Collaborators
Foundation for Chiropractic Education and Research (FCER)
Start date
2007-10
Primary completion
2008-09
Sex
All
Age range
from 18 Years to 60 Years
Results posted
Yes, on ClinicalTrials.gov
Countries
Canada
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Adults between 18 and 60 years old from the city and the surrounding Trois-Rivières with chronic cervical pain of non-traumatic origin (chronic or recurrent cervical pain that lasted at least 6 months) Exclusion Criteria: Exclusion criteria for the project are: * Surgery to the cervical spine * Neoplasms * Severe osteoarthritis * Ankylosing spondylitis * Hypertension * Referred pain in the cervical area * Central or peripheric nervous system dysfunction * Vascular disease * Treated cardiovascular disease * Inflammatory or infectious disease of the cervical spine * Metabolic or endocrine diseases * Pregnancy * Specific rehabilitation training for the neck or already under manual therapy for neck pain * Patient suffering from dizziness, vertigo or headache suspected to be cervicogenic or of unknown origin will not be involved in the study.

Canadian sites (1)

FacilityCityProvince
Université du Québec à Trois-RivièresTrois-RivièresQuebec

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT00566930