About this trial
The purpose of this clinical trial is to use a digital recording device integrated with an incentive spirometer to record a patient's deep breathing lung training following abdominal surgery. Through this digital recording, it will be possible to effectively assess the daily frequency, duration, depth of deep breaths, and the volume of inhalation performed by the patient during their breathing exercises. This will transform the previously difficult-to-describe deep breathing training into a digital record, allowing healthcare professionals to quickly evaluate the patient's condition. Patients can also monitor their own respiratory function changes, leading to positive health promotion benefits, accelerating their postoperative recovery, and simultaneously reducing healthcare costs and improving medical quality.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
1. Patients undergoing bariatric surgery
2. Patients could cooperate with conducting incentive spirometry before and after the operation.
Disqualifiers
1. Patients with contra-indication for incentive spirometry.
2. Patients could not deeply breathe with pulmonary vital capacity less than 10mL/kg.
3. Patients could not cooperate with conducting incentive spirometry before and after the operation.
4. Other causes judged by the Principal Investigator
Trial design
Parallel
Treatments tested in this trial
digitalized incentive spirometry
Devicedigitalized incentive spirometry
traditional incentive spirometry
Devicetraditional incentive spirometry
Treatment groups
Trial outcomes
Primary outcomes
Apnea/Hyponea Index
Post operative
Pulse oximetry change
Post operative
Secondary outcomes
Postoperative pulmonary complication
including atelectasis, pneumonia and respiratory failure
Locations
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: