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Therapy of Pain Syndromes According to McGill's Method in Physiotherapy

Primary Purpose

Vertebrogenic Pain Syndrome

Status

Completed

Phase

Not Applicable

Locations

Czechia

Study Type

Interventional

Intervention

Cervical pain

Thoracic pain

Lumbar pain

About this trial

This is an interventional treatment trial for Vertebrogenic Pain Syndrome focused on measuring pain syndrome, efficiency, stabilization, McGill method

Eligibility Criteria

20 Years - 55 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

cervical pain syndrome
thoracic pain syndrome
lumbar pain syndrome

Exclusion Criteria:

red falgs

Sites / Locations

Charles University, Faculty of physical education and sport

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Arm Label

Cervical pain

Thoracic pain

Lumbar pain

Arm Description

Only patients with positive Cervical pain syndrome.

Only patients with positive Thoracic pain syndrome.

Only patients with positive Lumbar pain syndrome.

Outcomes

Primary Outcome Measures

Pain relief

change in pain perception measured on a visual analog scale - from 0 (without pain) to 10 (maximum pain)

multi-segmental efficiency

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

Secondary Outcome Measures

Full Information

NCT ID

NCT04695665

First Posted

January 3, 2021

Last Updated

January 5, 2021

Sponsor

Charles University, Czech Republic

1. Study Identification

Unique Protocol Identification Number

NCT04695665

Brief Title

Therapy of Pain Syndromes According to McGill's Method in Physiotherapy

Official Title

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

Study Type

Interventional

2. Study Status

Record Verification Date

January 2021

Overall Recruitment Status

Completed

Study Start Date

March 15, 2020 (Actual)

Primary Completion Date

March 15, 2020 (Actual)

Study Completion Date

May 30, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title

Principal Investigator

Name of the Sponsor

Charles University, Czech Republic

4. Oversight

Studies a U.S. FDA-regulated Drug Product

Studies a U.S. FDA-regulated Device Product

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study

Vertebrogenic Pain Syndrome

Keywords

pain syndrome, efficiency, stabilization, McGill method

7. Study Design

Primary Purpose

Treatment

Study Phase

Not Applicable

Interventional Study Model

Parallel Assignment

Masking

ParticipantInvestigator

Allocation

Non-Randomized

Enrollment

30 (Actual)

8. Arms, Groups, and Interventions

Arm Title

Cervical pain

Arm Type

Active Comparator

Arm Description

Only patients with positive Cervical pain syndrome.

Arm Title

Thoracic pain

Arm Type

Active Comparator

Arm Description

Only patients with positive Thoracic pain syndrome.

Arm Title

Lumbar pain

Arm Type

Active Comparator

Arm Description

Only patients with positive Lumbar pain syndrome.

Intervention Type

Other

Intervention Name(s)

Cervical pain

Intervention Description

Exercise program for cervical spine according to McGill's approach.

Intervention Type

Other

Intervention Name(s)

Thoracic pain

Intervention Description

Exercise program for thoracic spine according to McGill's approach.

Intervention Type

Other

Intervention Name(s)

Lumbar pain

Intervention Description

Exercise program for lumbar spine according to McGill's approach.

Primary Outcome Measure Information:

Title

Pain relief

Description

change in pain perception measured on a visual analog scale - from 0 (without pain) to 10 (maximum pain)

Time Frame

4 weeks, 2 times a week exercising for 60 minutes

Title

multi-segmental efficiency

Description

Time Frame

4 weeks

10. Eligibility

Sex

All

Minimum Age & Unit of Time

20 Years

Maximum Age & Unit of Time

55 Years

Accepts Healthy Volunteers

Eligibility Criteria

Inclusion Criteria: cervical pain syndrome thoracic pain syndrome lumbar pain syndrome Exclusion Criteria: red falgs

Overall Study Officials:

First Name & Middle Initial & Last Name & Degree

Jitka Malá, Ph.D.

Organizational Affiliation

Charles University, Faculty of physical education and sport

Official's Role

Principal Investigator

Facility Information:

Facility Name

Charles University, Faculty of physical education and sport

City

Praha

Country

Czechia

12. IPD Sharing Statement

Plan to Share IPD

Learn more about this trial

Therapy of Pain Syndromes According to McGill's Method in Physiotherapy

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