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Informing Low-acuity Emergency Department Patients of Non-emergent Resources

Informing Low-acuity Emergency Department Patients of Non-emergent Healthcare Resources Following Discharge to Decrease Emergency Department Utilization

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06350266
Enrollment
6242
Registered
2024-04-05
Start date
2024-04-25
Completion date
2024-12-27
Last updated
2025-01-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Emergency Service, Hospital

Brief 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.

Interventions

BEHAVIORALInformation about healthcare resources

Text messages will be sent following discharge from the emergency department; text may also be modified in the (online and/or printed) discharge summary packet.

Sponsors

Geisinger Clinic
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Masking description

Patients will be aware of their own messages but not of messages sent to other patients or in other arms.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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 information in the EHR or because the patient opted out * Admitted to hospital * Already included in intervention in past 365 days

Design outcomes

Primary

MeasureTime frameDescription
Return to Geisinger EDwithin 120 days following day of dischargeED visit (yes/no)

Other

MeasureTime frameDescription
PCP visitwithin 60 days following day of dischargePCP appointment attended (yes/no)
Telehealth appointment madewithin 60 days following day of dischargeTelehealth appointment made (yes/no)
Telehealth appointment attendedwithin 60 days following day of dischargeTelehealth appointment attended (yes/no)
PCP appointment madewithin 60 days following day of dischargePCP appointment made (yes/no)
Any of the suggested actions takenwithin 60 days following day of dischargePCP called or visited, telehealth appointment attended, or PCP or telehealth appointment made (yes/no)
Urgent care visitwithin 60 days following day of dischargeUrgent care appointment attended (yes/no)
Call made to PCPwithin 60 days following day of dischargeRecord of patient call to PCP (yes/no)

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026