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Effect of Physiotherapeutic Interventions on Quality of Life in Patients With Chronic Low Back Pain. (Study 2)

NCT03309540 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2018-10-12

No results posted yet for this study

Summary

The purpose of this study is to investigate the effect on QoL, PI and the AROM° in patients with non-specific chronic low back pain. This after following an episode of 6 weeks 2 times a week physiotherapeutic back rehabilitation according to the 4 times T method by orthopaedic disorder ® (4MTOR®). The results in this research will be analyzed and reported. In this study, 7 dependent variables will be independently examined relative to 2 independent variables.

Conditions

  • Chronic Low Back Pain
  • Physiotherapy
  • Quality of Life
  • Range of Motion
  • Pain Intensity

Interventions

OTHER

Physioterapy intervention

In the experimental group (EGR), the 4MTOR® treatment method will be used for LBP. This 4MTOR® uses the following steps in a decision tree: T1 Testing (Physiotherapeutic examination), T2 Triggering (Manual Techniques), T3 Taping (Elastic Tape) and T4 Training (medical rehabilitation exercises). The participants in the SGR received a sham multimodal physiotherapeutic intervention as control intervention, in which Sham technique were applied. The interventions consisted of combining Sham manual interventions, elastic tapes according to Kaze32 and Evidence Based Practice Therapy (Appendix III). The protocol in the SGR follows the similar steps: Testing, Taping, Triggering and Training like the 4MTOR®.

Sponsors & Collaborators

  • Committee of Medical Ethics University Hospital University of Brussels, B.U.N. 143201627110.

    collaborator UNKNOWN

  • Ethias liability policy: 45.147.458, insurance for the experiment on human subjects.

    collaborator UNKNOWN

  • The EuroQol Research Foundation

    collaborator OTHER

  • This research is supported by the Fysio Science Institute® and is a non-profit institution.

    collaborator UNKNOWN

  • Vrije Universiteit Brussel

    lead OTHER

Principal Investigators

  • Peter P Vaes, PhD · University of Brussels, faculty of Rehabilitation science and physical therapy, faculty of Pharmacy and medicine, Brussels, Belgium

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
FACTORIAL

Eligibility

Min Age
20 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-10-31
Primary Completion
2018-12-31
Completion
2018-12-31

Countries

  • Belgium

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03309540 on ClinicalTrials.gov