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Respiratory Exercise Diary in Major Abdominal Surgery

T

TC Erciyes University

Status

Enrolling

Conditions

Pulmonary Complication

Treatments

Other: respiratory exercise diary

Study type

Interventional

Funder types

Other

Identifiers

NCT06078644
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Details and patient eligibility

About

Postoperative pulmonary complications are common and lead to increased morbidity and mortality in patients. These complications are observed especially after major surgical interventions. Breathing exercises performed with or without the use of a device are extremely important in preventing postoperative pulmonary complications. Breathing exercises that increase total lung capacity by encouraging the use of the diaphragm reverse alveolar collapse and postoperative hypoxemia. This study aim to determine the effect of postoperative respiratory exercise diary use in patients undergoing major abdominal surgery on dyspnea, fatigue, respiratory parameters (respiratory rate, SPO2, cough, sputum), early pulmonary complications, spirometry use and functional capacity.The research is planned to be conducted in a single-blind, randomized controlled manner. In the study, 60 patients (30 intervention and 30 control) who underwent major abdominal surgery will be included.Data will be collected using the Patient Introduction Form, Visual Analogue Scale, Medical Research Board Scale, 2-minute walk test, breathing exercise diary and patient follow-up chart.Patients in the intervention and control groups will be visited by the researcher for 3 postoperative days, respiratory parameters, cough, and sputum status will be recorded in the patient follow-up chart, and the use of a respiratory exercise diary will be evaluated.

Enrollment

60 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Undergoing elective surgery
  • Receiving general anesthesia
  • Having major abdominal surgery (colorectal surgery, gastrectomy, liver resection, pancreatectomy)
  • Staying in the general surgery service for at least 3 days after the surgery
  • Becoming literate

Exclusion criteria

  • Psychoactive drug use
  • Having Alzheimer's or dementia
  • Having chronic respiratory diseases (COPD, asthma)

Trial design

Primary purpose

Diagnostic

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

60 participants in 2 patient groups

Intervention group
Experimental group
Description:
Patients in this group will be asked to perform breathing exercises in the form of using a spirometer 10 times every hour during the preoperative period while they are awake for three days, starting from the first day after the surgery. Patients in this group will be given a breathing exercise diary.
Treatment:
Other: respiratory exercise diary
Control group
No Intervention group
Description:
Patients in this group will not undergo any treatment and will continue to receive care according to their clinical routine. In the clinic, when patients are admitted to the hospital, nurses give them a spirometer during the pre-operative period and it is stated that they should use it before and after the surgery. After the data collection tools are applied to the patients in this group, they will be asked how many times a day they use a spirometry.

Trial contacts and locations

1

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Central trial contact

Erdoğan Mütevelli Sözüer, Prof.

Data sourced from clinicaltrials.gov

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