Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07185828

Informing Low-acuity Emergency Department Patients of Non-emergent Resources (2)

Informing Low-acuity Emergency Department Patients of Non-emergent Healthcare Resources Following Discharge to Decrease Emergency Department Utilization (2)

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
8,286 (estimated)
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). In this campaign, patients will be assigned to receive or not receive outreach following ED discharge with a low-acuity visit designation. Outreach will occur via a text message the day after discharge from the ED as well as information added to the patient's after visit summary (AVS). Depending on the assigned condition, it will include calls to see their primary care provider (PCP) or use an Intelligent Triage tool. The study will assess whether ED use within the following 120 days differs across patients in different outreach conditions (current standard practice vs contact your PCP vs use Intelligent Triage). It will also examine whether patients follow through on the message-specific calls to action differently across conditions.

Conditions

Interventions

TypeNameDescription
BEHAVIORALContact your PCPText messages will be sent and discharge paperwork will be modified to encourage contacting a primary care provider.
BEHAVIORALUse Intelligent TriageText messages will be sent and discharge paperwork will be modified to encourage using Intelligent Triage.

Timeline

Start date
2025-04-15
Primary completion
2026-05-01
Completion
2026-08-01
First posted
2025-09-22
Last updated
2026-03-13

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT07185828. Inclusion in this directory is not an endorsement.