Institute of Health Sciences, Saglik Bilimleri University
Istanbul, Turkey (Türkiye)
Location status: Recruiting
Location contact
Beyza SU, MSc.
PRINCIPAL_INVESTIGATOR
Sibel YİLMAZ SAHİN, Assoc Prof
CONTACT
NCT Number: NCT07549555
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.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Not applicable
Istanbul, Turkey (Türkiye)
Location status: Recruiting
Beyza SU, MSc.
PRINCIPAL_INVESTIGATOR
Sibel YİLMAZ SAHİN, Assoc Prof
CONTACT
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.
Thoracic surgery is a method used in the treatment of diseases of the lungs, pleura, chest wall, and mediastinum. The primary problems encountered by patients postoperatively include improper patient positioning, incision pain, ineffective coughing, reduced lung volume, postoperative pulmonary complications, inadequate airway clearance, frozen shoulder on the side of the thoracotomy, postural abnormalities, and persistent chest wall tension. These issues, particularly pulmonary complications, can delay patient recovery, prolong hospital stays, and increase morbidity and mortality. Tube thoracostomy is a one-way drainage system that facilitates the drainage of fluid and air from the pleural space, maintains negative pressure, and allows for lung expansion. Additionally, it allows for the administration of therapeutic medications into the pleural space. Patients should be educated on respiratory exercises-such as coughing, balloon inflation, and the use of a triflowmeter-to facilitate lung expansion and secretion clearance, and they should be encouraged to perform these exercises regularly. A review of the literature reveals no studies investigating the effectiveness of manual vibration in patients with chest tubes. It is believed that this technique may shorten the duration of chest tube placement. Additionally, due to the lack of cost-effectiveness of mechanical vibration, supply issues, the inability to use it effectively on all patients in clinical settings, the recommendation for more frequent use, and the necessity of applying it based on the patient's needs rather than at regular intervals (such as every two hours)-a determination that must be made by the nurse closely monitoring the patient- it is anticipated that the manual vibration technique will provide greater benefits at regular intervals without incurring additional costs, as it adapts to the patient's needs and the clinic's operational schedule throughout the day.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
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.
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.
Time frame: 1 day
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
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
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.
Contact information is provided by the study sponsor or research team.
Beyza SU, MSc.
CONTACT
Sibel YİLMAZ SAHİN, Assoc Prof
CONTACT
Saglik Bilimleri Universitesi
Other
The Effect of Manual Chest Wall Vibration on Respiratory Functions and Chest Tube Duration in Patients Undergoing Thoracic Surgery
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07634861
Respiratory Tract Diseases, Thoracic Diseases
Shanghai, China
View Trial DetailsNCT05521789
Lung Diseases, Lung Neoplasms
Washington D.C., District of Columbia, United States
View Trial DetailsNCT07028593
Lung Diseases, Lung Neoplasms
Wuhan, China
View Trial DetailsNCT07250230
Agnosia, Analgesia
Zhengzhou, Henan, China
View Trial Details