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ACUTE EFFECT OF DIAPHRAGMATIC BREATHING ON POSTOPERATIVE UPPER TRAPEZIUS PAIN

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

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07634588
Acronym
TRAP-BREATHE
Enrollment
38
Registered
2026-06-09
Start date
2026-06-05
Completion date
2026-08-01
Last updated
2026-06-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Myofascial Pain Syndrome, Neck Pain, Work-Related Musculoskeletal Disorders

Keywords

Upper Trapezius Pain, Diaphragmatic Breathing, Soft Tissue Mobilization, Percussive Therapy, Operating Room Nurses, Pressure Pain Threshold, Neck Disability Index, Musculoskeletal Pain, Acute Pain

Brief 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.

Detailed description

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.

Interventions

BEHAVIORALDiaphragmatic Breathing Exercise

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

OTHERSoft Tissue Mobilization

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.

Sponsors

Istanbul Aydın University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
22 Years to 55 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Pain IntensityImmediately 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.

Secondary

MeasureTime frameDescription
Neck Disability IndexImmediately 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.

Countries

Turkey (Türkiye)

Contacts

CONTACTFatma Çavdarcı
cvdrcftm@gmail.com+905374590918

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 10, 2026