Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT06350266 · ClinicalTrials.gov registry record · NA
Informing Low-acuity Emergency Department Patients of Non-emergent Resources
A NA study, sponsored by Geisinger Clinic.
- Completed
- Registry status
- NA
- Development phase
- 6,242
- Enrollment target
NCT06350266: Completed NA study, sponsored by Geisinger Clinic.
NCT06350266 is a NA study that has completed, run by Geisinger Clinic. The registered enrollment target is 6,242 participants, above the 1,403-participant average among 58,714 other NA trials with a reported enrollment target (345% higher). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06350266, a NA study, has completed, sponsored by Geisinger Clinic.
- COMPLETED
- Registry status
- NA
- Development phase
- 6,242 participants
- Enrollment target
Study 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.
Primary Outcome
ED visit (yes/no)
Interventions
- BEHAVIORAL Information about healthcare resources
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 6,242 participants |
| Start Date | 2024-04-25 |
| Est. Completion | 2024-12-27 |
| Phase | NA |
What the finished NCT06350266 record still lists
NCT06350266 is an interventional study that assigns participants to a tested intervention. Its 6,242 participants enrollment target places it among the larger protocols in the corpus, above the 1,403-participant average among 58,714 other NA trials with a reported enrollment target (345% higher).
The record links to 0 conditions, and to 1 intervention - of which Information about healthcare resources is the first listed.
NCT06350266 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT06350266 about?
NCT06350266 is a clinical study titled "Informing Low-acuity Emergency Department Patients of Non-emergent Resources". 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 tha...
What is the current status of trial NCT06350266?
This trial is currently completed. It is a NA study. The enrollment target is 6,242 participants. The study started on 2024-04-25. Estimated completion is 2024-12-27.
What interventions are being tested in trial NCT06350266?
The interventions under investigation include: Information about healthcare resources (BEHAVIORAL).
Who is sponsoring clinical trial NCT06350266?
This trial is sponsored by Geisinger Clinic, which has 107 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT06350266's enrollment target sits among peer trials
6,242 22nd of 2000 higher than 1,979 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT03960099 · 6,250 participants · NA
Pictographs for Preventing Wrong-Patient Errors in NICUs
- NCT05440851 · 6,250 participants · NA
Platform of Randomized Adaptive Clinical Trials in Critical Illness
- NCT06566170 · 6,250 participants
A Real-World Comparative Study of Donanemab (LY3002813) Plus Usual Care Versus Usual Care Alone in US Participants With Early Symptomatic Alzheimer's Disease
- NCT04884802 · 6,254 participants · NA
The GUARDIAN Trial
Similar registry start date
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia
- NCT07125183 · started 2026-12 · Phase 2
Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma
- NCT07292298 · started 2026-11 · Phase 2
Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates
- NCT04263285 · started 2026-10 · NA
Treatment of Depression Post-SCI