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Text Messaging Follow-up From ED

The Role of Text Messaging in Follow-up Appointments for Patients Discharged From the Emergency Department

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03370978
Enrollment
0
Registered
2017-12-13
Start date
2019-05-01
Completion date
2020-05-01
Last updated
2021-04-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Text Messaging

Brief summary

Ensuring follow-up for patients after discharge from the emergency department (ED) has long been a concern for ED care providers. The current technology of text messaging may be able to assist us in improving follow-up rates. In addition, having a quick and easy communication tool to be in touch with providers may improve overall patient satisfaction. This study is designed to evaluate the usage of text messaging to improve follow-up appointment compliance from the Emergency Department. In this study, a prospective randomized controlled trial (RCT) will be performed (involving patients scheduled by Emergency Department Nurse Navigators to follow up with Family Medicine) in which patients will be randomized to a texting appointment reminder versus standard-of-care (no texting reminder) group. Texted patients will receive reminders 3 days and 1 day prior to their follow-up appointment. In addition, the patients will have the ability to text back-and-forth with the Nurse Navigators in order to ask questions/request clarification if needed. Chart review will be performed of both groups to evaluate the number of follow-up appointments that patients attended versus rescheduled versus did not attend/reschedule. These values will then be compared to the retrospective chart review previously performed to evaluate for non-inferiority of text messaging as a means of improving patient attendance at follow-up appointments.

Interventions

BEHAVIORALText Messaging

To communicate with intervention patients after discharge from the ED, we will use a bidirectional text messaging service provided by another physician's research group within the University of Iowa. The nurse navigator will enter the patient's study identification number, first and last name and cell phone onto a secure study website established by this research group. Patients will, as previously mentioned, have had their cell phone number tested in the text messaging system prior to leaving the Emergency Department (this includes the control group). Patient's will receive a text message 3 days, and 1 day, prior to their scheduled follow-up appointment with Family Medicine (this appointment having been scheduled through the Emergency Department Nurse Navigators). Each text message will remind the patient of the date/time of their appointment, and provide them a link containing a map with the location of their appointment.

Sponsors

University of Iowa
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. At least 18 years old 2. Able to read, write and communicate in English - English as the primary language 3. Has a phone with capabilities for text messaging 4. Identifies oneself as someone who is comfortable with text messaging. 5. To follow-up with Family Medicine as outpatient (Scheduled through Emergency Department Nurse Navigators). 6. Evaluated in the University of Iowa Hospitals and Clinics Emergency Department

Exclusion criteria

1. Absence of one or more inclusion criteria 2. Not able to provide informed consent or participate due to limited decision-making ability. 3. Prisoner 4. Previously has followed with the University of Iowa Hospitals and Clinics Family Medicine (i.e., would not be a new patient establishing care).

Design outcomes

Primary

MeasureTime frameDescription
Attending Primary Care AppointmentLess than 6 monthsAttending appointment versus rescheduling versus not showing

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026