NCT06535347

Brief Summary

The goal of this campaign is to reduce unnecessary emergency department (ED) visits by encouraging patients with high acuity visits to follow up with an appropriate primary care provider (PCP) or specialist and therefore obtain appropriate care outside of the ED. 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 and information added to the patient's after visit summary, and will include a contact number to schedule and hyperlink to allow self-scheduling. The study will assess whether ED use differs across patients in different outreach conditions. It will also examine whether patients followed through on the calls to action in the messages differently across conditions.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
6,814

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Aug 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

July 8, 2024

Completed
25 days until next milestone

First Posted

Study publicly available on registry

August 2, 2024

Completed
7 days until next milestone

Study Start

First participant enrolled

August 9, 2024

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 6, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 6, 2025

Completed
Last Updated

June 5, 2025

Status Verified

June 1, 2025

Enrollment Period

8 months

First QC Date

July 8, 2024

Last Update Submit

June 4, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Return to ED

    ED visit (yes/no)

    within 120 days following day of discharge

Other Outcomes (8)

  • PCP/specialist appointment made

    within 7 days following day of discharge

  • PCP/specialist appointment made

    within 14 days following day of discharge

  • PCP/specialist appointment made

    within 30 days following day of discharge

  • +5 more other outcomes

Study Arms (3)

Control

NO INTERVENTION

This arm will receive no intervention outside of usual care.

Experimental: Schedule Follow-Up Visit - 1 message

EXPERIMENTAL

This arm will receive a text message (at 1 day post-ED discharge) and information added to the patient's after visit summary providing a number and patient portal hyperlink via which to schedule an ED follow-up appointment.

Behavioral: Information about scheduling a follow-up appointment

Experimental: Schedule Follow-Up Visit - 2 messages

EXPERIMENTAL

This arm will receive text messages (at 1 day and 8 days post-ED discharge) and information added to the patient's after visit summary providing a number and patient portal hyperlink via which to schedule an ED follow-up appointment.

Behavioral: Information about scheduling a follow-up appointment

Interventions

Text message(s) will be sent following discharge from the emergency department, along with an after visit summary.

Also known as: Text messages, Information
Experimental: Schedule Follow-Up Visit - 1 messageExperimental: Schedule Follow-Up Visit - 2 messages

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • \>= 18 years of age
  • ED visit rated as high acuity (level L2 or L3)
  • Discharged from ED in past 24 hours
  • Attributed to a Geisinger PCP in Community Medicine Service Line

You may not qualify if:

  • Have an appointment scheduled within 7 days following discharge with a primary care provider or specialist
  • Institutionalized
  • Cannot be contacted via the communication modality being used in the study (i.e., SMS), due to insufficient/missing contact information in the electronic health record or because the patient opted out
  • Admitted to hospital
  • Eloped from ED
  • Left ED without being seen
  • Deceased prior to messaging

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Geisinger Health System

Danville, Pennsylvania, 17822, United States

Location

MeSH Terms

Conditions

Emergencies

Condition Hierarchy (Ancestors)

Disease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • Amir Goren, PhD

    Geisinger Clinic

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Masking Details
Patients will be aware of their own messages but will not be aware of other messages.
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
‪Program Director, Behavioral Insights Team

Study Record Dates

First Submitted

July 8, 2024

First Posted

August 2, 2024

Study Start

August 9, 2024

Primary Completion

April 6, 2025

Study Completion

April 6, 2025

Last Updated

June 5, 2025

Record last verified: 2025-06

Locations