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.
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