NCT05245773

Brief Summary

This study will evaluate a 30-day post-discharge intervention using an automated SMS platform to monitor patients and facilitate communication with their primary care practice. The population will be patients who receive care from participating practices and are discharged from an inpatient stay. In addition to the usual phone call from their practice, patients will be randomized to enrollment in the program, wherein they will receive automated SMS messages on a tapering schedule over 30 days.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
5,000

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Mar 2022

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

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 8, 2022

Completed
10 days until next milestone

First Posted

Study publicly available on registry

February 18, 2022

Completed
1 month until next milestone

Study Start

First participant enrolled

March 29, 2022

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 4, 2023

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

February 3, 2023

Completed
Last Updated

February 27, 2023

Status Verified

February 1, 2023

Enrollment Period

9 months

First QC Date

February 8, 2022

Last Update Submit

February 24, 2023

Conditions

Keywords

Post-DischargePrimary CareAutomated Hovering

Outcome Measures

Primary Outcomes (1)

  • Post-discharge acute care utilization

    A composite, binary measure indicating whether a patient visited the ED or was readmitted to inpatient care after discharge from the hospital.

    30 days post-discharge

Secondary Outcomes (7)

  • Post-discharge days in the hospital

    30 days post-discharge

  • Post-discharge acute care utilization

    7 and 60 days post-discharge

  • Post-discharge ED visit

    7, 30, and 60 days post-discharge

  • Readmission

    7, 30, and 60 days post-discharge

  • Time from discharge to first acute care visit

    30 days post-discharge

  • +2 more secondary outcomes

Study Arms (2)

30-day automated hovering + usual care

EXPERIMENTAL

The intervention arm will get the usual post-discharge call from their practice, typically within 2 business days of discharge. In addition, they will be enrolled in the 30-day automated texting program, wherein they will receive check-in messages on a tapering schedule; they will be free to opt out at any time. They can also message into the platform at any time. Any needs identified through the platform will be escalated to their primary care practice, and they will receive a follow-up phone call from practice staff to address their needs.

Other: Automated SMS program to support post-discharge transitions of care

Usual care

NO INTERVENTION

The control arm will continue to receive the usual post-discharge call from their practice, typically within 2 business days of discharge.

Interventions

The intervention will consist of automated text messages on a tapering schedule over the course of 30 days post-discharge, with responses escalated back to the practice care management team. After initial enrollment messages, patients will receive check-in messages on a tapering schedule over the course of 30 days. For the first week they will receive 3 total messages; the second week they will receive a total of 2 messages. For the last 2 weeks they will receive weekly messages. If a patient need is identified, the request will be escalated to the practice (triaged by the care management RN) for a follow up phone call. Patients will be able to reach out at any time by sending a message to the same number, and they will be entered into the same pathway. For any escalated need, patients will receive a follow up phone call from the practice staff.

Also known as: MORE-PC
30-day automated hovering + usual care

Eligibility Criteria

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

You may qualify if:

  • The study subjects will be medium to high risk (UPHS risk score 4 and above; an internally developed and validated score assessing a patient's risk for readmission) adult (age ≥ 18) patients of the Penn Primary Care Practices who are discharged home from acute inpatient care in the broad Philadelphia region as identified in HealthShare Exchange (HSX) reports

You may not qualify if:

  • This study will exclude discharges who do not meet criteria for transitional care management. These criteria include discharges after 1) planned chemotherapy admissions; 2) certain scheduled surgeries, including spinal surgery, joint replacements, gastric bypass, transurethral resection of the prostate, gynecologic surgeries, and transplants; 3) obstetrics admissions.
  • We will exclude patients from re-enrollment during the study period (once they have been enrolled once, they will not be enrolled again). We will also exclude patients being discharged to home hospice.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Pennsylvania School of Medicine

Philadelphia, Pennsylvania, 19104, United States

Location

Related Publications (1)

  • Bressman E, Long JA, Burke RE, Ahn A, Honig K, Zee J, McGlaughlin N, Balachandran M, Asch DA, Morgan AU. Automated Text Message-Based Program and Use of Acute Health Care Resources After Hospital Discharge: A Randomized Clinical Trial. JAMA Netw Open. 2024 Apr 1;7(4):e243701. doi: 10.1001/jamanetworkopen.2024.3701.

Study Officials

  • Anna Morgan, MD, MSHP

    University of Pennsylvania

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
PARALLEL
Model Details: Pragmatic randomized controlled trial with intervention and control arm
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 8, 2022

First Posted

February 18, 2022

Study Start

March 29, 2022

Primary Completion

January 4, 2023

Study Completion

February 3, 2023

Last Updated

February 27, 2023

Record last verified: 2023-02

Locations