SMS-Based Follow-Ups to Improve Post-Discharge Surgical Outcomes
Surgical Site Infection
About this trial
This is an interventional supportive care trial for Surgical Site Infection focused on measuring Text-message reminder, Post-operative medication, Behavioral Research, Social Research, Short Message Service (SMS)
Eligibility Criteria
Inclusion Criteria:
- Patient has a working cell phone that can send and receive SMS/Multimedia Messaging Service (MMS) over the next three months
- Patient has a working cell phone with a camera
- Being able to read and write fluently in English
- All patients identified in the Electronic Medical Record (EMR) with International Classification of Diseases (ICD)-10 codes for patients who underwent procedures with external wounds and can be at risk of surgical site infection (SSI). Only patients falling under the categories of 'Major Diagnostic' and 'Major Therapeutic' will be considered.
Exclusion Criteria:
- Patient deceased prior to discharge
- Patient transferred to another hospital
- Patient has a terminal illness with less than 3-month expected survival
- Vulnerable populations including patients who are in the middle of a pregnancy or prisoners
Sites / Locations
- Grady Health System
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
SMS-based reminders
Control group
This group will receive consistent medication reminders, as per the patient's prescribed frequency, and weekly surveys prompting them to report their pain level and an image of their surgical site. They will also receive a monthly questionnaire via SMS to assess patient satisfaction with the intervention and changes in medication adherence behaviors.
The control group will not receive medication reminders or questions regarding their pain or surgical site. This group will receive a monthly questionnaire via SMS to assess patient satisfaction with the intervention and changes in medication adherence behaviors.