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Effect of Neurophysiological Facilitation Techniques Applied in Addition to Pilates-based Exercise Training in Individuals With Fibromyalgia on Respiratory Parameters, Fatigue and Quality of Life

NCT07017101 · Status: ENROLLING_BY_INVITATION · Phase: NA · Type: INTERVENTIONAL · Enrollment: 31

Last updated 2025-06-12

No results posted yet for this study

Summary

The aim of our study was to examine the effect of neurophysiological facilitation techniques applied in addition to pilates-based exercise training in individuals with fibromyalgia on body composition, core stabilization, respiratory parameters, fatigue and quality of life.

Conditions

  • Fibromyalgia (FM)

Interventions

OTHER

PILATES BASED EXERCISE TRAINING WITH REFORMER

Participants will only be given training on pilates-based exercises with reformers. Breathing, which are the 5 key elements of clinical pilates exercises after the first evaluation to individuals, Focus, rib cage placement, shoulder placement, head and neck placement will be taught. Whole Participants will be informed about the reformer instrument and work schedule. Exercises 2 days a week, 6 Will be applied throughout the week.

OTHER

NEUROPHYSIOLOGICAL FASCILITATION TECHNIQUES

In addition to reformer-based pilates training, participants will be given Neurophysiological facilitation techniques training. Neurophysiological facilitation techniques are non-invasive, easy to apply, the physiotherapist is active It consists of exercises made with guidance and active participation of the patient. These techniques are any Does not contain an electrotherapy current. In this study, the neurophysiological Facilitation techniques, perioral stimulation, intercostal tension, anterior basal lift, vertebral pressure, medium Graded manual pressure and abdominal co-contraction techniques and each technique for 15 seconds Will be applied. Neurophysiological facilitation techniques are used to repeat 10 sessions each session throughout the treatment. It will be done.

Sponsors & Collaborators

  • Okan University

    lead OTHER

Principal Investigators

  • Gamze Aydın · Okan Üniversitesi

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-02-23
Primary Completion
2025-06-21
Completion
2025-06-25

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 NCT07017101 on ClinicalTrials.gov