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Recruiting

NCT Number: NCT07185828

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 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.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Geisinger

Danville, Pennsylvania, 17822, United States

Location status: Recruiting

Location contact

Amir Goren, PhD

CONTACT

[email protected]

570-214-4395

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Contact your PCP

Behavioral

Text messages will be sent and discharge paperwork will be modified to encourage contacting a primary care provider.

Use Intelligent Triage

Behavioral

Text messages will be sent and discharge paperwork will be modified to encourage using Intelligent Triage.

Primary outcomes

  1. Return to Geisinger ED

    Time frame: within 120 days following day of discharge

    ED visit (yes/no)

Other outcomes

  1. PCP appointment made

    Time frame: within 60 days following day of discharge

    PCP appointment made (yes/no)

  2. PCP visit

    Time frame: within 60 days following day of discharge

    PCP appointment attended (yes/no)

  3. Telehealth appointment made

    Time frame: within 60 days following day of discharge

    Telehealth appointment made (yes/no)

  4. Telehealth appointment attended

    Time frame: within 60 days following day of discharge

    Telehealth appointment attended (yes/no)

  5. Call made to PCP

    Time frame: within 60 days following day of discharge

    Record of patient call to PCP (yes/no)

  6. Urgent care visit

    Time frame: within 60 days following day of discharge

    Urgent care appointment attended (yes/no)

  7. Used Intelligent Triage

    Time frame: within 60 days following day of discharge

    Used the Intelligent Triage tool (yes/no)

  8. Any of the suggested actions taken

    Time frame: within 60 days following day of discharge

    PCP called or visited, telehealth appointment attended, or PCP or telehealth appointment made, or Intelligent Triage tool used (yes/no)

Study contacts

Contact information is provided by the study sponsor or research team.

Amir Goren, PhD

CONTACT

[email protected]

570-214-4395

Sponsors and collaborators

Lead sponsor

Geisinger Clinic

Other

Registry information

Official study title

Informing Low-acuity Emergency Department Patients of Non-emergent Healthcare Resources Following Discharge to Decrease Emergency Department Utilization (2)

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Sep 22, 2025
Registry last updated
Jul 23, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.