Hospitalism Clinical Trial
Official title:
Implementing 30-day Post- Discharge Community Health Worker Pairings for Patients at High-Risk for Readmission (C-CAT Study)
This study focuses on pairing community health workers (CHWs) with patients that are high risk for readmission prior to hospital discharge in order to assess differences in hospital readmission rates, ED visits, patient satisfaction and provider satisfaction as compared to patients without community health worker pairings at discharge.
This study is a randomized controlled trial of 1200 adult patients admitted to internal
medicine units that will examine the effectiveness of pairing patients that are high risk for
readmission with community health workers at the time of hospital discharge on hospital
readmission rates, emergency room visits, adherence to post-discharge medical appontments,
and satisfaction with care. During this study, community health workers will partner with
patients for 30 days after discharge from the hospital to address barriers to care via phone
contacts, home visits, and accompanying patients to medical appointments/other non-clinical
supportive care.
AIM 1) Determine if patients randomly assigned to the intervention group have lower rates of
hospital readmission than the control group at the end of the intervention.
Hypothesis 1.1 Study participants in the intervention group will have lower rates of
post-discharge thirty day readmission than the study participants in the control group at the
end of the intervention.
AIM 2) Determine if patients randomly assigned to the intervention group will have less
emergency room visits than the control group at the end of the intervention
Hypothesis 2.1 Study participants in the intervention group will have less emergency room
visits than the study participants in the control group at the end of the intervention.
AIM 3) Determine if patients randomly assigned to the intervention group have more adherence
to post-discharge appointments that study group participants in the control group at the end
of the intervention
Hypothesis: 3.1 Study participants in the intervention group will have higher rates of
attendance at post-discharge medical appointments than the study participants in the control
group at the end of the intervention.
AIM 4) Determine if patients randomly assigned to the intervention group have higher levels
of patient psychosocial support and satisfaction with post-discharge care than the control
group
Hypothesis 4.1: Study participants in the intervention group will have higher levels of
patient psychosocial support and satisfaction with post-discharge care than the study
participants in the control group at the end of the intervention.
AIM 5) Determine if Primary Care Physicians of patients randomly assigned to the intervention
group have higher levels of satisfaction with post-discharge care than Primary Care Providers
of patients in the control group
Hypothesis 5.1: Primary Care Physicians of patients randomly assigned to the intervention
group have higher levels of satisfaction with post-discharge care than Primary Care Providers
of patients in the control group
After reviewing the fact sheet and consenting to enrollment by signing the informed consent
form, patients will randomized to the intervention or control groups of the study.
STUDY PROCEDURES
Intervention Arm Group:
Patients randomized to the intervention group will be paired with community health workers
prior to discharge from the hospital and patient- centered program goals will be established.
A patient questionnaire (10-15 minutes) will be administered to intervention study
participants by a study coordinator prior to discharge. A chart review will be performed for
all intervention group participants by study coordinators prior to patient discharge.
Patient-CHW pairings will continue for thirty days post-discharge and will include phone
contacts, home visits, accompanying patients to medical appointments and other non-clinical
supportive care. Both intervention group participants and primary care providers (PCPs) of
intervention study participants will complete questionnaires 30-60 days after hospital
discharge to assess certain patient ( 10 minute questionnaire; via phone) and primary care
provider ( 5 minute questionnaire via email) perceptions (Please see Aim 4 and Aim 5). CHWs
will document patient encounters in a REDCap database and complete patient care notes in
EPIC. All intervention study participants readmitted within thirty days of prior discharge
will be administered a readmission questionnaire by study coordinators. A chart review for
readmitted study participants will also be performed by study staff. A REDCap database will
be used to store all questionnaire and chart review data. Readmission rates, ED visits, PCP
appointment compliance, patient/ PCP will be tracked.
Control Arm Group:
Those randomized to the control group will receive usual care without a community heath
worker pairing. A patient questionnaire (10-15 minutes) will be administered to intervention
study participants by a study coordinator prior to discharge. A chart review will be
performed for all control group participants by study coordinators prior to patient
discharge. Both control group participants and primary care providers (PCPs) of intervention
study participants will complete questionnaires 30-60 days after hospital discharge to assess
certain patient ( 10 minute questionnaire; via phone) and primary care provider ( 5 minute
questionnaire via email) perceptions (Please see Aim 4 and Aim 5). A REDCap database will be
used to store all questionnaire and chart review data. Readmission rates, ED visits, PCP
appointment compliance, patient/ PCP perceptions will be tracked.
Three groups of research subjects will be assessed: the intervention study group, the control
study group, and the PCPs of the patients enrolled in the study.
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