Effect of the Mobile Self-input Tool of Incentive Spirometer (RCT)

Gastrectomy Clinical Trial

Official title:

Effect of the Mobile Self-input Tool of Incentive Spirometer on Its Usage by Patients : a Randomized Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03569332
• Other study ID #: 2018-02-135
• Status: Completed
• Phase: N/A
• Start date: April 16, 2018
• Est. completion date: July 10, 2018

Study information

• Verified date: June 2018
• Source: Samsung Medical Center
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study evaluates the effectiveness of the mobile self-input tool providing alarm and visual motivation, how much more it can encourage practicing of incentive spirometer undergoing post-operative patients under general anesthesia. Half of participants will receive the mobile self-input tool providing alarm, and their practicing rate will be sent to Nurse's Dashboard. While the other half will receive the mobile self-input tool, but it won't contain alarm function and their practicing rate won't be sent to Nurse's Dashboard, either.

Description:

1. Background : Active respiratory therapy like incentive spirometer is needed to prevent pulmonary complications for patients undergoing post-operative under general anesthesia. But in many cases, patients don't practicing it for their pain, or they just forget doing it. And medical staffs are having difficulties in checking how well the patients follow the directions for doing incentive spirometer. Insufficient practicing incentive spirometer and deep breathing cause delay their health recovery.

Therefore, we want to make some tools which can encourage the patients' practicing for incentive spirometer and also supply the objective achievement of patients to medical staffs.

2. Objective : This study evaluates the effectiveness of the mobile self-input tool providing alarm and visual motivation, how much more it can encourage practicing of incentive spirometer undergoing post-operative patients under general anesthesia.

3. Design: RCT (randomized controlled trial)

4. Setting: In the Department of Gastrointestinal Surgery at the Samsung Medical Center

5. Enrollment : 44 patients undergoing gastrectomy.

6. Intervention 6-1) For study group : participants on study group are received self-input tool with alarm system on tablet.

Alarm is provided only if insufficient practice (less than 10 times/hour) from 9am to 9pm. The practicing rate is sent to Nurse's Dashboard.

6-2) For control group : participants on control group are received self-input tool without alarm on tablet. Their practicing rate is not sent to Nurse's Dashboard.

7. Scoring by practicing incentive spirometer from 9 am to 9 pm. (Only when a subject practiced more than 10 times per hour, the subject get 10 points) (Full score 240)

8. Study period : for 48hrs from one day to 3rd day after patient's operation

9. Satisfaction survey (SUS) after study(3rd day after operation)

Recruitment information / eligibility

• Status: Completed
• Enrollment: 44
• Est. completion date: July 10, 2018
• Est. primary completion date: May 17, 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• A subject undergoing total gastrectomy or subtotal gastrectomy by robotic surgery, laparoscopic surgery or open surgery

• A subject who got surgery under general anesthesia

• A Subject receiving a prescription of using incentive spirometer

• A subject who voluntarily agrees and signs

Exclusion Criteria:

• Disorientation

• Unscheduled emergency surgery

• a subject who has difficulty in active breathing exercise due to problems such as heart disease, brain disease, chronic lung disease, etc.

Related Conditions & MeSH terms

• Gastrectomy

Intervention

Other:
• Alarm
Alarm is provided from 9am to 9pm. Alarm is active every 50 minutes if the exercise goal(10 times/hour) hasn't satisfied.
• Nurse's dashboard
Wireless data transmission system The practicing rate of participants on study group is sent to Nurse's Dashboard. It is only to display.

Locations

Country	Name	City	State
Korea, Republic of	Samsung Medical Center	Seoul	Gangnam

Sponsors (2)

Lead Sponsor	Collaborator
Samsung Medical Center	Samsung Electronics

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Total number of practicing incentive spirometer that subjects input by themselves on the mobile self-input tool and scoring by practicing incentive spirometer from 9 am to 9 pm.	Only when a subject practiced more than 10 times per hour, the subject get 10 points	Only collecting the numbers of practicing between 9 am and 9 pm for two days, from 1st day to 3rd day after operation.
Secondary	Collecting subject's medical records related to pulmonary complication	such as body temperature, laboratory results and Chest X-ray.	From one day after subject's operation to the date the subject leaves(discharges) the hospital. (Average duration is for 4~5days)
Secondary	Satisfaction Survey for mobile self-input tool	Scoring by the answers of the Questionnaire of Satisfaction (SUS)	3rd day after operation