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Comparison of Two Different Fascial Treatments

NCT06715969 · Status: ENROLLING_BY_INVITATION · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2024-12-04

No results posted yet for this study

Summary

The aim of this study is to compare the different effects of two different fascial treatments on pain, flexibility and Asian architecture.

2 different groups 8 sessions, two different fascial treatments will be applied in accordance with the intake criteria, the individuals will be re-evaluated before the treatment, after 8 sessions of treatment and 3 months after the end of the study.

Conditions

  • Low Back Pain, Mechanical

Interventions

OTHER

Myofascial Release Techniques

Separate techniques will be applied to the parts of the thoracolumbal fascia that surround the erector spina, quadratus lumborum, latissimus dorsi muscles and extend in that direction to patients in the MFR group. Techniques will continue for 180 seconds, tissue shift will be carried further as relaxation is achieved. Applications Total 8 sessions will be applied twice a week by an experienced physiotherapist.

OTHER

Myofascial Induction Techniques

MIT will be applied to the lumbal region by a physiotherapist trained and experienced in fascial treatments to patients in the MIT group. Applications 2 sessions per week, a total of 8 sessions will be applied, with an average of 20-25 minutes. The application principles of this technique will be as follows. * Induction of the lumbal interfacial triangle region (stroke application) (3 min) * Induction of the lumbal interfacial triangle region (deep induction application) (3 min) * Cross-hands myofascial induction (3 min)

OTHER

classıcal phsyotherapy

15 sessions of mictowave diathermy (MDD), Vacuum Interference, Infraruj and Classic waist exercise program will be applied to patients in this group.

Sponsors & Collaborators

  • Hasan Kalyoncu University

    collaborator OTHER

  • Doğan Burak Endamli

    lead OTHER

Principal Investigators

  • kezban bayramlar, profesör · Hasan Kalyoncu University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2024-11-15
Primary Completion
2024-12-15
Completion
2025-04-15

Countries

  • Turkey (Türkiye)

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 NCT06715969 on ClinicalTrials.gov