Effect of Manual Chest Wall Vibration on Respiratory Function and Chest Tube Duration After Thoracic Surgery

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorSaglik Bilimleri Universitesi

About this trial

This study was conducted to determine the effects of a manual vibration technique applied to the chest wall on the duration of chest tube placement, secretion clearance, and hemodynamic parameters in patients with chest tubes.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Having undergone thoracic surgery

Having a chest tube in the postoperative period

Being hemodynamically stable

Agreeing to participate in the study

Disqualifiers

Severe cardiac instability

Patients unable to tolerate the procedure due to neurological or cognitive impairment

Clinical conditions that would prevent the application of vibration to the chest wall

Patients diagnosed with pneumonia

Trial design

Design model

Parallel

Treatments tested in this trial

  • Chest Wall Oscillation

    Procedure/Surgery

    Manual chest wall vibration is applied with the patient in a semi-Fowler's position during the expiratory phase of breathing. The practitioner places both hands flat on the chest wall and delivers gentle, rhythmic vibrations, starting from the lower lobes and progressing toward the upper lobes. Patients are instructed to inhale slowly through the nose and exhale using a pursed-lip breathing technique with a 1:2 inspiration-expiration ratio. The procedure is performed for approximately 5 minutes, corresponding to about 10 respiratory cycles, and is typically applied during the patient's rest period following routine care.

  • Conventional Control

    Behavioral

    Control group patients were informed about the study and provided written consent. They received only routine nursing care, with no additional interventions applied. Baseline measurements were taken at 0 minutes, including dyspnea (MBS), pain (VNRS), vital signs, and arterial blood gas values. Following routine care, the same parameters were reassessed at 3, 5, and 10 minutes and recorded. No manual chest wall vibration was performed; only standard clinical monitoring was maintained. The same assessment protocol was repeated in the evening session.

Treatment groups

60 Participants
are divided into 2 treatment groups
Group A: Chest Wall Oscillation GroupActive comparator 1 intervention
Group B: Conventional Control GroupSham comparator 1 intervention

Trial outcomes

Primary outcomes

1

Patient Follow-Up Form

Changes in respiratory and hemodynamic parameters (including respiratory rate, peripheral oxygen saturation, heart rate, blood pressure), dyspnea severity (Modified Borg Scale), and pain intensity (Visual Numeric Rating Scale) measured before the intervention and at 0, 1, 5, 10, and 15 minutes after the intervention.

Time frame
1 day

Secondary outcomes

1

Post-Operative Respiratory Status Questionnaire

A 6-item patient-reported questionnaire using a 5-point Likert scale will be used to assess postoperative respiratory symptoms and adherence to breathing exercises. Higher scores indicate better outcomes.

Time frame
1 day
2

Questionnaire on manual chest wall vibration therapy

A 9-item Likert-type questionnaire will be used to assess patient comfort, perceived benefit, and satisfaction with manual chest wall vibration. Higher scores indicate more favorable outcomes.

Time frame
1 day

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.