ACUTE EFFECT OF DIAPHRAGMATIC BREATHING ON POSTOPERATIVE UPPER TRAPEZIUS PAIN

Condition(s) studied

Investigational drug(s) / intervention(s)

Diaphragmatic Breathing Exercise: Participants will perform diaphragmatic breathing exercises for 5 minutes in a seated position under physiotherapist supervision.

Soft Tissue Mobilization: Soft tissue mobilization techniques will be applied to the upper trapezius muscle for 5 minutes.

Percussive Therapy: Percussive therapy will be applied to the upper trapezius muscle for 5 minutes using a massage device.

Study summary

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.

Eligibility

Primary outcome measure(s)

• Pain Intensity — 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.

Trial sites (1)

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