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NCT07185828 · ClinicalTrials.gov registry record · NA
Informing Low-acuity Emergency Department Patients of Non-emergent Resources (2)
A NA study of Emergency Service, Hospital and Behavior Change Interventions, sponsored by Geisinger Clinic.
- Recruiting
- Registry status
- NA
- Development phase
- 8,286
- Enrollment target
- 1
- Study location
NCT07185828 is a NA study of Emergency Service, Hospital and Behavior Change Interventions that is actively recruiting participants, run by Geisinger Clinic. The registered enrollment target is 8,286 participants. The trial reports 1 study location across 1 state.
The verdict
NCT07185828, a NA study of Emergency Service, Hospital and Behavior Change Interventions, is actively recruiting participants, sponsored by Geisinger Clinic.
- RECRUITING
- Registry status
- NA
- Development phase
- 8,286 participants
- Enrollment target
- 1
- Study location
Study 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 Studied
Interventions
- BEHAVIORAL Contact your PCP
- BEHAVIORAL Use Intelligent Triage
Study Locations (1)
Pennsylvania
- Geisinger - Danville
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 8,286 participants |
| Start Date | 2025-04-15 |
| Est. Completion | 2026-08 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07185828
The ClinicalTrials.gov registry entry for NCT07185828 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 8,286 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Geisinger Clinic, which has 107 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Emergency Service, Hospital appearing as the primary indexed condition, and to 2 interventions - of which Contact your PCP is the first listed.
NCT07185828 reports 1 study location spanning 1 distinct geographic area - top geographies include Pennsylvania.
Frequently Asked Questions
What is clinical trial NCT07185828 about?
NCT07185828 is a clinical study titled "Informing Low-acuity Emergency Department Patients of Non-emergent Resources (2)". 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 discharg...
What is the current status of trial NCT07185828?
This trial is currently recruiting. It is a NA study. The enrollment target is 8,286 participants. The study started on 2025-04-15. Estimated completion is 2026-08.
What conditions does trial NCT07185828 study?
This clinical trial studies the following conditions: Emergency Service, Hospital, Behavior Change Interventions.
What interventions are being tested in trial NCT07185828?
The interventions under investigation include: Contact your PCP (BEHAVIORAL), Use Intelligent Triage (BEHAVIORAL).
Who is sponsoring clinical trial NCT07185828?
This trial is sponsored by Geisinger Clinic, which has 107 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07185828 being conducted?
This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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