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
| Type | Name | Description |
|---|---|---|
| BEHAVIORAL | Contact your PCP | Text messages will be sent and discharge paperwork will be modified to encourage contacting a primary care provider. |
| BEHAVIORAL | Use Intelligent Triage | Text 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.