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Clinical Trials/NCT04695665
NCT04695665CompletedNot Applicable

The Effectiveness of McGill's Method in the Treatment of Vertebrogenic Algic Syndrome

Charles University, Czech Republic1 site in 1 country30 target enrollmentStarted: March 15, 2020Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
30
Locations
1
Primary Endpoint
multi-segmental efficiency

Study Overview

Brief Summary

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.

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 Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Participant, Investigator)

Eligibility Criteria

Ages
20 Years to 55 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • cervical pain syndrome
  • thoracic pain syndrome
  • lumbar pain syndrome

Exclusion Criteria

  • red falgs

Outcomes

Primary Outcomes

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

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)

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Charles University, Czech Republic
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Malá Jitka

assistant professor

Charles University, Czech Republic

Study Sites (1)

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