Preventive Care of Chronic Cervical Pain and Disabilities
NCT ID: NCT00566930
Last Updated: 2012-09-28
Study Results
Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.
View full resultsBasic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
117 participants
INTERVENTIONAL
2007-10-31
2008-09-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
FACTORIAL
TREATMENT
DOUBLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
1
No interventions assigned to this group
2
spinal manipulation
spinal manipulation
Monthly cervical spinal manipulation
3
Spinal manipulation + exercises
Spinal manipulation + exercises
Monthly cervical spine manipulation and daily home exercises
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
spinal manipulation
Monthly cervical spinal manipulation
Spinal manipulation + exercises
Monthly cervical spine manipulation and daily home exercises
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
* 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.
18 Years
60 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Foundation for Chiropractic Education and Research (FCER)
OTHER
Université du Québec à Trois-Rivières
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Martin Descarreaux
Professor
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Martin Descarreaux, PhD
Role: PRINCIPAL_INVESTIGATOR
Université du Québec à Trois-Rivières
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Université du Québec à Trois-Rivières
Trois-Rivières, Quebec, Canada
Countries
Review the countries where the study has at least one active or historical site.
References
Explore related publications, articles, or registry entries linked to this study.
Martel J, Dugas C, Dubois JD, Descarreaux M. A randomised controlled trial of preventive spinal manipulation with and without a home exercise program for patients with chronic neck pain. BMC Musculoskelet Disord. 2011 Feb 8;12:41. doi: 10.1186/1471-2474-12-41.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
FCER Grant #06-03-02
Identifier Type: -
Identifier Source: secondary_id
Chronic cervical pain UQTR
Identifier Type: -
Identifier Source: org_study_id