Clinical Trials Directory

Trials / Completed

CompletedNCT06350266

Informing Low-acuity Emergency Department Patients of Non-emergent Resources

Informing Low-acuity Emergency Department Patients of Non-emergent Healthcare Resources Following Discharge to Decrease Emergency Department Utilization

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
6,242 (actual)
Sponsor
Geisinger Clinic · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The goal of this campaign is to reduce unnecessary visits to a Geisinger emergency department (ED)/encourage patients with high acuity visits to follow up with an appropriate Geisinger provider. 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, as well as information added to the patient's after visit summary, and will includecalls to action to see their Geisinger CMSL PCP either in person or virtually. The study will assess whether ED use differs across patients in different outreach conditions. It will also examine whether patients follow through on the message-specific calls to action in the messages differently across conditions.

Conditions

Interventions

TypeNameDescription
BEHAVIORALInformation about healthcare resourcesText messages will be sent following discharge from the emergency department; text may also be modified in the (online and/or printed) discharge summary packet.

Timeline

Start date
2024-04-25
Primary completion
2024-12-27
Completion
2024-12-27
First posted
2024-04-05
Last updated
2025-01-09

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT06350266. Inclusion in this directory is not an endorsement.