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

T

Taipei Medical University

Status

Not yet enrolling

Conditions

Sleep Apnea, Obstructive
Bariatric Surgery Candidate

Treatments

Device: digitalized incentive spirometry
Device: traditional incentive spirometry

Study type

Interventional

Funder types

Other

Identifiers

NCT06132100
N202303047

Details and patient eligibility

About

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.

Full description

After thoracoabdominal and neurosurgery procedures, an incentive spirometer is commonly employed for deep breathing exercises to prevent or improve potential postoperative pulmonary atelectasis, increase lung capacity, promote the clearance of respiratory secretions, and maintain chest mobility to reduce postoperative complications related to lung collapse. This medical device and the respiratory training process are essential components of Enhanced Recovery After Surgery (ERAS) protocols, which integrate postoperative care processes to enhance recovery, reduce hospitalization times, and minimize postoperative complications. Currently, clinical guidelines typically recommend patients to perform 200-600 deep inhalations per day after surgery. Despite the simplicity and effectiveness of using an incentive spirometer for deep breathing exercises, the observation of patients' usage, recording of the number and duration of exercises, and tracking of their deep inhalation volumes have become crucial tasks for respiratory therapists, nurses, and physicians in the postoperative setting, consuming significant time and resources.

Generally, using an incentive spirometer requires patients to perform 200-600 deep breaths a day. According to a 2018 medical literature estimate in the United States, approximately 9.7 million surgical procedures annually involve the use of incentive spirometers, with human resource costs for assisting patients in their use and assessing the effectiveness of their pulmonary rehabilitation reaching approximately one billion US dollars.

Enrollment

200 estimated patients

Sex

All

Ages

20 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

    1. Patients undergoing bariatric surgery
    1. Patients could cooperate with conducting incentive spirometry before and after the operation.

Exclusion criteria

    1. Patients with contra-indication for incentive spirometry.
    1. Patients could not deeply breathe with pulmonary vital capacity less than 10mL/kg.
    1. Patients could not cooperate with conducting incentive spirometry before and after the operation.
    1. Other causes judged by the Principal Investigator

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

200 participants in 2 patient groups, including a placebo group

traditional incentive spirometry
Placebo Comparator group
Description:
patients with traditional incentive spirometry
Treatment:
Device: traditional incentive spirometry
digitalized incentive spirometry
Experimental group
Description:
patients with digitalized incentive spirometry
Treatment:
Device: digitalized incentive spirometry

Trial contacts and locations

0

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Central trial contact

Shih-Chiang Shen, MD

Data sourced from clinicaltrials.gov

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