MORE-PC: A 30-day Automated SMS Program to Support Post-discharge Transitions of Care

Sponsor
University of Pennsylvania (Other)
Overall Status
Recruiting
CT.gov ID
NCT05245773
Collaborator
UnitedHealth Group (Industry)
5,000
1
2
6.1
818.2

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Automated SMS program to support post-discharge transitions of care
N/A

Detailed Description

Background:

Current models of post-discharge care management are time and labor intensive, limited in scope, and inconvenient from the patient perspective, particularly when they have a need arise. Automation can significantly scale up patient touches while reserving staff time for concrete patient needs. Text messaging has been shown to enhance patient engagement (as compared to calls) in many settings, possibly due to greater convenience and the potential for asynchronous interaction. We believe using automated text messaging messaging as the foundation of a post-discharge, primary care based care management program can increase patient engagement, allow for earlier and more frequent identification of needs, and improve post-discharge outcomes.

Objective:

To evaluate the impact of a 30-day post-discharge intervention using an automated SMS platform in addition to usual care as compared to usual care alone in a multi-clinic, pragmatic randomized controlled trial on acute care utilization, post-discharge follow-up appointment scheduling and show-rates, overall patient engagement, and overall patient-clinic encounters.

Description of Intervention:

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 enrollment, patients will receive an initial message asking them if they have a follow up appointment within the next 2 weeks. If they respond no, the practice will be notified to reach out and help them schedule an appointment.

Beginning the day after this introductory message, 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 (Monday, Wednesday and Friday); the second week they will receive a total of 2 messages (Tuesday and Thursday). For the last 2 weeks they will receive weekly messages (on Tuesdays). 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 throughout the 30 days 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 within 1 business day. Patients who do not respond to 3 consecutive messages will receive an additional check in message ensuring that they still want to be enrolled.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
5000 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Pragmatic randomized controlled trial with intervention and control armPragmatic randomized controlled trial with intervention and control arm
Masking:
None (Open Label)
Primary Purpose:
Health Services Research
Official Title:
MORE-PC: A 30-day Automated SMS Program to Support Post-discharge Transitions of Care
Actual Study Start Date :
Mar 29, 2022
Anticipated Primary Completion Date :
Sep 1, 2022
Anticipated Study Completion Date :
Oct 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: 30-day automated hovering + usual care

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
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.
Other Names:
  • MORE-PC
  • No Intervention: Usual care

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

    Outcome Measures

    Primary Outcome Measures

    1. Post-discharge acute care utilization [30 days post-discharge]

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

    Secondary Outcome Measures

    1. Post-discharge days in the hospital [30 days post-discharge]

      A continuous measure of total days spent in the hospital (in the ED or as an inpatient) after hospital discharge

    2. Post-discharge acute care utilization [7 and 60 days post-discharge]

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

    3. Post-discharge ED visit [7, 30, and 60 days post-discharge]

      A binary measure indicating whether a patient visited the ED after hospital discharge

    4. Readmission [7, 30, and 60 days post-discharge]

      A binary measure indicating whether a patient was readmitted after hospital discharge

    5. Time from discharge to first acute care visit [30 days post-discharge]

      A continuous measure of the time from discharge to either first ED visit or readmission

    6. Post-discharge follow up visit [14 days post-discharge]

      A binary measure indicating scheduling and completion of a follow up visit with the primary care practice

    7. Number of patient-practice interactions [30 days post-discharge]

      A continuous measure of non-visit interactions between the patient and practice (which will include a) telephone encounters [which are the end point of any needs identified through the automated messaging program] and b) EMR portal messages)

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • 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
    Exclusion Criteria:
    • 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.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of Pennsylvania School of Medicine Philadelphia Pennsylvania United States 19104

    Sponsors and Collaborators

    • University of Pennsylvania
    • UnitedHealth Group

    Investigators

    • Principal Investigator: Anna Morgan, MD, MSHP, University of Pennsylvania

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University of Pennsylvania
    ClinicalTrials.gov Identifier:
    NCT05245773
    Other Study ID Numbers:
    • 849348
    First Posted:
    Feb 18, 2022
    Last Update Posted:
    Mar 31, 2022
    Last Verified:
    Mar 1, 2022
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by University of Pennsylvania

    Study Results

    No Results Posted as of Mar 31, 2022