Nudging High-acuity Emergency Department Patients to Schedule a Follow-up Visit
1 other identifier
interventional
6,814
1 country
1
Brief Summary
The goal of this campaign is to reduce unnecessary emergency department (ED) visits by encouraging patients with high acuity visits to follow up with an appropriate primary care provider (PCP) or specialist and therefore obtain appropriate care outside of the ED. In this campaign, patients will be assigned to receive or not receive outreach following ED discharge that is aligned with the goal. Outreach will occur via a text message and information added to the patient's after visit summary, and will include a contact number to schedule and hyperlink to allow self-scheduling. The study will assess whether ED use differs across patients in different outreach conditions. It will also examine whether patients followed through on the calls to action in the messages differently across conditions.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Aug 2024
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 8, 2024
CompletedFirst Posted
Study publicly available on registry
August 2, 2024
CompletedStudy Start
First participant enrolled
August 9, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 6, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
April 6, 2025
CompletedJune 5, 2025
June 1, 2025
8 months
July 8, 2024
June 4, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Return to ED
ED visit (yes/no)
within 120 days following day of discharge
Other Outcomes (8)
PCP/specialist appointment made
within 7 days following day of discharge
PCP/specialist appointment made
within 14 days following day of discharge
PCP/specialist appointment made
within 30 days following day of discharge
- +5 more other outcomes
Study Arms (3)
Control
NO INTERVENTIONThis arm will receive no intervention outside of usual care.
Experimental: Schedule Follow-Up Visit - 1 message
EXPERIMENTALThis arm will receive a text message (at 1 day post-ED discharge) and information added to the patient's after visit summary providing a number and patient portal hyperlink via which to schedule an ED follow-up appointment.
Experimental: Schedule Follow-Up Visit - 2 messages
EXPERIMENTALThis arm will receive text messages (at 1 day and 8 days post-ED discharge) and information added to the patient's after visit summary providing a number and patient portal hyperlink via which to schedule an ED follow-up appointment.
Interventions
Text message(s) will be sent following discharge from the emergency department, along with an after visit summary.
Eligibility Criteria
You may qualify if:
- \>= 18 years of age
- ED visit rated as high acuity (level L2 or L3)
- Discharged from ED in past 24 hours
- Attributed to a Geisinger PCP in Community Medicine Service Line
You may not qualify if:
- Have an appointment scheduled within 7 days following discharge with a primary care provider or specialist
- Institutionalized
- Cannot be contacted via the communication modality being used in the study (i.e., SMS), due to insufficient/missing contact information in the electronic health record or because the patient opted out
- Admitted to hospital
- Eloped from ED
- Left ED without being seen
- Deceased prior to messaging
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Geisinger Cliniclead
Study Sites (1)
Geisinger Health System
Danville, Pennsylvania, 17822, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Amir Goren, PhD
Geisinger Clinic
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Masking Details
- Patients will be aware of their own messages but will not be aware of other messages.
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Program Director, Behavioral Insights Team
Study Record Dates
First Submitted
July 8, 2024
First Posted
August 2, 2024
Study Start
August 9, 2024
Primary Completion
April 6, 2025
Study Completion
April 6, 2025
Last Updated
June 5, 2025
Record last verified: 2025-06