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

Recruiting N/A Interventional Study
Emergency Service, Hospital Behavior Change Interventions
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Health Services Research
Participants needed
8,286 (estimated)
Sponsor
Geisinger Clinic · Other
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About This Trial
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 …
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * \>= 18 years of age * Geisinger ED visit rated as low acuity (L4 or L5) * Discharged from Geisinger ED in past 24 hours Exclusion Criteria: * Cannot be contacted via the communication modality being used in the study (i.e., SMS), due to insufficient/missing contact informati…
Contacts

Amir Goren, PhD

570-214-4395

agoren@geisinger.edu

CONTACT