Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
107 participants
OBSERVATIONAL
2020-02-01
2022-01-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Evaluation of How Different Dosages of Spinal Manipulation Modulate Spinal Stiffness in Participants With Back Pain
NCT03063177
Spinal Manipulation and Spinal Mobilization Effects in Participants With and Without Back Pain
NCT02660801
The Effect of a Single Spinal Manipulation on Cardiovascular Autonomic Activity
NCT03273868
Preventive Care of Chronic Cervical Pain and Disabilities
NCT00566930
Specific or Non-Specific Manipulation for Patients With Back Pain
NCT02883634
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.
COHORT
PROSPECTIVE
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Thoracic spinal manipulation
High velocity, low amplitude force manipulation
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Presenting non-specific back pain (chronic \>=3 months or recurrent complaint)
* Speaking French or English
Exclusion Criteria
* Non-musculoskeletal disorders pain
* Pregnancy
* Not eligible to spinal manipulation (if osteoporosis, vertebral fracture history, thoracic disk herniation)
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
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, Doctor of Chiropractic
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Martin Descarreaux, DC, PhD
Role: STUDY_DIRECTOR
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.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
UQTR-2020-SMTdose
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.