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ACUTE EFFECT OF DIAPHRAGMATIC BREATHING ON POSTOPERATIVE UPPER TRAPEZIUS PAIN (TRAP-BREATHE)

5. Juni 2026 aktualisiert von: FATMA ÇAVDARCI, Istanbul Aydın University

EVALUATION OF THE ACUTE EFFECTS OF DIAPHRAGMATIC BREATHING EXERCISES ADDED TO SOFT TISSUE MOBILIZATION AND PERCUSSIVE THERAPY ON PAIN, FUNCTIONALITY, AND PRESSURE PAIN THRESHOLD IN THE UPPER TRAPEZIUS MUSCLE OF SURGICAL NURSES AFTER SURGERY

This randomized controlled trial aims to investigate the acute effects of diaphragmatic breathing exercises added to soft tissue mobilization and percussive therapy on pain intensity, functional disability, and pressure pain threshold in operating room nurses experiencing upper trapezius pain after surgery-related work activities.

Participants will be operating room nurses working in a hospital operating theater who report upper trapezius pain and tenderness within 30 minutes after completing a surgical procedure. Eligible participants will be randomly assigned to either an intervention group receiving soft tissue mobilization, percussive therapy, and diaphragmatic breathing exercises, or a control group receiving soft tissue mobilization and percussive therapy alone.

Pain intensity will be assessed using the Visual Analog Scale (VAS), functional disability using the Neck Disability Index (NDI), and mechanical pain sensitivity using Pressure Pain Threshold (PPT) measurements. Assessments will be performed immediately before and after a single treatment session. The study aims to determine whether the addition of diaphragmatic breathing exercises provides additional benefits in reducing pain and improving function in the acute postoperative working period of operating room nurses.

Studienübersicht

Detaillierte Beschreibung

Operating room nurses are exposed to prolonged static postures, repetitive upper extremity movements, and sustained neck and shoulder loading during surgical procedures. These occupational demands frequently result in upper trapezius pain, tenderness, and functional limitations. Acute musculoskeletal symptoms experienced after surgical procedures may negatively affect both occupational performance and quality of life.

Soft tissue mobilization and percussive therapy are commonly used physiotherapy interventions for reducing muscle tension, improving local circulation, and decreasing pain sensitivity. Diaphragmatic breathing exercises may further contribute to pain reduction through autonomic nervous system regulation, parasympathetic activation, and decreased physiological stress responses. Although each intervention has been investigated separately, evidence regarding their combined acute effects in operating room nurses is limited.

The purpose of this randomized controlled trial is to evaluate whether the addition of diaphragmatic breathing exercises to a treatment protocol consisting of soft tissue mobilization and percussive therapy provides additional benefits for pain reduction, functional improvement, and pressure pain threshold in operating room nurses experiencing upper trapezius pain following surgery-related work activities.

Participants meeting the eligibility criteria will be randomly allocated to one of two groups. The intervention group will receive soft tissue mobilization, percussive therapy, and diaphragmatic breathing exercises, while the control group will receive soft tissue mobilization and percussive therapy only. All interventions will be administered during a single treatment session under physiotherapist supervision.

Outcome measures will include pain intensity assessed by the Visual Analog Scale (VAS), functional disability assessed by the Neck Disability Index (NDI), and mechanical pain sensitivity assessed by Pressure Pain Threshold (PPT) measurements using a digital algometer. Measurements will be obtained immediately before and immediately after the intervention session.

The findings of this study may contribute to the development of practical physiotherapy strategies for managing acute work-related upper trapezius pain among operating room nurses and may help identify the additional value of diaphragmatic breathing exercises within a multimodal physiotherapy approach.

Studientyp

Interventionell

Einschreibung (Geschätzt)

38

Phase

  • Unzutreffend

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienkontakt

Studienorte

    • Eyalet/Yerleşke
      • Istanbul, Eyalet/Yerleşke, Türkei (türkiye), 34520
        • Istanbul Aydin University
        • Kontakt:

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Erwachsene

Akzeptiert gesunde Freiwillige

Nein

Beschreibung

Inclusion Criteria:

  • Aged between 22 and 55 years.
  • Operating room nurse actively working in the hospital operating theater.
  • Reporting upper trapezius pain and tenderness within 30 minutes after completion of a surgical procedure.
  • Willing to participate and able to provide written informed consent.

Exclusion Criteria:

  • History of trauma, surgery, or chronic disease affecting the neck or shoulder region.
  • Regular participation in breathing exercise programs.
  • Psychiatric disorders requiring anxiolytic or antidepressant medication.
  • Pregnancy.
  • Skin disease, infection, or open wound in the treatment area.
  • Severe cardiovascular disease or uncontrolled hypertension.
  • Contraindications to manual therapy, soft tissue mobilization, percussive therapy, or breathing exercises.

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: Zufällig
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: Experimental Group
Participants will receive 5 minutes of soft tissue mobilization, 5 minutes of percussive therapy, and 5 minutes of diaphragmatic breathing exercises in a single treatment session.
Participants will perform diaphragmatic breathing exercises for 5 minutes in a seated position under physiotherapist supervision.
Soft tissue mobilization techniques will be applied to the upper trapezius muscle for 5 minutes.
Percussive therapy will be applied to the upper trapezius muscle for 5 minutes using a massage device.
Aktiver Komparator: Control Group
Participants will receive 5 minutes of soft tissue mobilization and 5 minutes of percussive therapy in a single treatment session.
Soft tissue mobilization techniques will be applied to the upper trapezius muscle for 5 minutes.
Percussive therapy will be applied to the upper trapezius muscle for 5 minutes using a massage device.

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Pain Intensity
Zeitfenster: Immediately before intervention and immediately after intervention (single session)
Pain intensity will be assessed using the Visual Analog Scale (VAS). The Visual Analog Scale ranges from 0 to 10 points, where 0 indicates no pain and 10 indicates the worst imaginable pain. Higher scores indicate greater pain severity. Change from pre-intervention to immediately post-intervention will be analyzed.
Immediately before intervention and immediately after intervention (single session)

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Neck Disability Index
Zeitfenster: Immediately before intervention and immediately after intervention (single session)
Neck-related disability will be assessed using the Neck Disability Index (NDI). The Neck Disability Index consists of 10 items with a total score ranging from 0 to 50 points. A score of 0 indicates no disability and 50 indicates maximum disability. Higher scores indicate greater disability and poorer neck function. Change from pre-intervention to immediately post-intervention will be analyzed.
Immediately before intervention and immediately after intervention (single session)

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Geschätzt)

5. Juni 2026

Primärer Abschluss (Geschätzt)

1. Juli 2026

Studienabschluss (Geschätzt)

1. August 2026

Studienanmeldedaten

Zuerst eingereicht

2. Juni 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

5. Juni 2026

Zuerst gepostet (Tatsächlich)

9. Juni 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

9. Juni 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

5. Juni 2026

Zuletzt verifiziert

1. Juni 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

NEIN

Beschreibung des IPD-Plans

Individual participant data will not be shared to protect participant confidentiality and privacy.

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

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