- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04695665
Therapy of Pain Syndromes According to McGill's Method in Physiotherapy
January 5, 2021 updated by: Malá Jitka, Charles University, Czech Republic
The Effectiveness of McGill's Method in the Treatment of Vertebrogenic Algic Syndrome
The goal of this study is to determine the applicability of McGill ́s method to patients with diagnoses, collectively referred to as Vertebrogenic Algic syndrome, by comparing the measured data of proband with different diagnosis locations Vertebrogenic Algic syndrome in the Czech Republic.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
This is a pilot experimental research involving 10 probands diagnosed with Vertebrogenic Algic syndrome in the cervical spine, 10 probands diagnosed with Vertebrogenic Algic syndrome in the thoracic spine and 10 probands diagnosed with Vertebrogenic Algic syndrome in the lumbar spine.
Each participant undergo a kinesiological examination according to the McGill ́s principles together with an SF-36 questionnaire.
Measured values are compared and provided a basis for testing the hypotheses.
The study uses methods of research, observation, querying and comparison of collected data.
Study Type
Interventional
Enrollment (Actual)
30
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Praha, Czechia
- Charles University, Faculty of physical education and sport
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 53 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- cervical pain syndrome
- thoracic pain syndrome
- lumbar pain syndrome
Exclusion Criteria:
- red falgs
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: Cervical pain
Only patients with positive Cervical pain syndrome.
|
Exercise program for cervical spine according to McGill's approach.
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Active Comparator: Thoracic pain
Only patients with positive Thoracic pain syndrome.
|
Exercise program for thoracic spine according to McGill's approach.
|
Active Comparator: Lumbar pain
Only patients with positive Lumbar pain syndrome.
|
Exercise program for lumbar spine according to McGill's approach.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Pain relief
Time Frame: 4 weeks, 2 times a week exercising for 60 minutes
|
change in pain perception measured on a visual analog scale - from 0 (without pain) to 10 (maximum pain)
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4 weeks, 2 times a week exercising for 60 minutes
|
multi-segmental efficiency
Time Frame: 4 weeks
|
comparison of the effectiveness of therapy of the three evaluated groups against each other by Short Form (SF36) Healthy survey questionnaire, the scale from 100 to 900, lower value indicate a higher effect
|
4 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Jitka Malá, Ph.D., Charles University, Faculty of physical education and sport
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 15, 2020
Primary Completion (Actual)
March 15, 2020
Study Completion (Actual)
May 30, 2020
Study Registration Dates
First Submitted
January 3, 2021
First Submitted That Met QC Criteria
January 4, 2021
First Posted (Actual)
January 5, 2021
Study Record Updates
Last Update Posted (Actual)
January 6, 2021
Last Update Submitted That Met QC Criteria
January 5, 2021
Last Verified
January 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Vlasák, McGill
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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-
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Fondazione Don Carlo Gnocchi OnlusCompleted
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