Automated Caller and Text Message Reminders for Reducing Appointment No-Shows
Text Message + Automated Caller (Intervention)
Other Study
Summary
Study start date: November 5, 2024
Actual date on which the first participant was enrolled.This study is focused on improving the attendance rate of patients at their scheduled outpatient appointments. Penn Medicine has noticed that less than 75% of these appointments are completed, which can cause longer wait times and reduce access to care. To address this, the study is testing if adding an automated phone call to the existing text message reminders can help reduce the number of missed appointments. The target group includes patients who are identified as having a higher risk of not showing up, according to a specific risk model. By finding a more effective reminder method, the study aims to improve appointment completion rates and enhance the efficiency of healthcare operations. During the study, participants are divided into two groups. One group receives the usual text message reminder, while the other gets both the text and an automated phone call. All participants are patients who have already agreed to receive text reminders and have an in-person appointment during the study. The study lasts for two weeks, and throughout this period, researchers track whether patients confirm, cancel, or miss their appointments. The outcomes of this trial will help Penn Medicine decide on the most effective reminder strategy to use in the future, potentially leading to better appointment adherence and healthcare service efficiency.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.32925 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Other Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Group I
Active ComparatorStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location