Using Digitalized Incentive Spirometers to Assist Postoperative Rehabilitation of Abdominal Surgery Patients

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age20-75
SponsorTaipei Medical University Shuang Ho Hospital

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 volunteers

Qualifiers

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

Design model

Parallel

Treatments tested in this trial

  • digitalized incentive spirometry

    Device

    digitalized incentive spirometry

  • traditional incentive spirometry

    Device

    traditional incentive spirometry

Treatment groups

200 Participants
are divided into 2 treatment groups
Group A: traditional incentive spirometryPlacebo comparator 1 intervention
Group B: digitalized incentive spirometryExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Apnea/Hyponea Index

Post operative

Time frame
7 - 10 days
2

Pulse oximetry change

Post operative

Time frame
7 - 10 days

Secondary outcomes

1

Postoperative pulmonary complication

including atelectasis, pneumonia and respiratory failure

Time frame
7-10 days

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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