App for Acute Pain Service in Major Surgery

Seoul National University

Status: Enrolling

Conditions: Patient Satisfaction; Pain, Postoperative; Smartphone; Mobile Applications

Treatments: Device: A new smart device application (Smart APS)

Study type: Interventional

Funder types: Other

Identifiers

NCT06014918

2304-053-1420

Details and patient eligibility

About

The app will be installed on the patient's smartphone before surgery. Patients will receive reminders to record their pain intensity and opioid-related side effects at the pre-determined time points until at least 2 days after surgery. The patient's compliance with the reminders will be assessed. On the second postoperative day, their satisfaction with pain control and app usage will be evaluated. Patients can also provide feedback on any issues they have encountered with the app during the study period.

Full description

Following admission, the application will be installed on the enrolled patient's smartphone prior to surgery, and the patient will be instructed on the content of the program and how to use it. Educational videos within the app about postoperative pain control will be introduced to the patient at this time. At the pre-determined time points, until at least 2 days post-operatively, the patient will be reminded of the assessment via an alarm function and will enter post-operative pain intensity using an 11-point numeric rating scale or verbal rating scale and the presence of opioid-related side effects into the application. If a patient responds to the alarm 2 or more times per day, they will be considered to be compliant. Postoperative opioid consumption using patient-controlled analgesia and the amount of rescue analgesics will be assessed. Patients will be assessed with a survey on postoperative day 2 for overall satisfaction with pain control and usage of the application. Patients will also be able to provide feedback via the application or research staff on any errors or inconveniences they may have experienced while using the application throughout the study.

Enrollment: 60 estimated patients

Sex: All

Ages: 19 to 70 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Adult patients aged 19 to 70 years who are scheduled for regular major surgery
• American Society of Anesthesiologists (ASA) physical status classification I or II
• Patients who are using a smartphone and are not expected to have any restrictions on application use

Exclusion criteria

• Unable to communicate
• Patients under the age of 19 and over the age of 70
• Patients who, in the opinion of the investigator or study staff, are not appropriate for this study

Trial design

Primary purpose: Supportive Care

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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60 participants in 1 patient group

Patients using a new application

Experimental group

Description:

Patients will enter pain intensity and opioid analgesic side effects using a new application named 'Smart APS', developed for acute pain services, and later assess for adherence and satisfaction with the application use.

Treatment:

Device: A new smart device application (Smart APS)