- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02087072
Collaborative Home Visits to Reduce Hospital Readmissions and Improve Medication Use During Transitions of Care
COLLABORATIVE HOME VISITS TO REDUCE HOSPITAL READMISSIONS AND IMPROVE MEDICATION USE DURING TRANSITIONS OF CARE
The primary objective is to develop a sustainable practice model emphasizing home visits by a collaborative physician and pharmacist team to decrease unplanned emergency department visits and hospital readmissions at 30 and 90 days for high-risk home bound patients. Secondary objectives include (1) tracking the number, type, and severity of adverse drug events (ADE) and potential adverse drug events (pADE) that occur following hospital discharge and (2) resolving any identified ADE and pADE within 7 days of hospital discharge.
Adult patients will be scheduled for a home visit by the Healthy at Home Columbus program at the time of hospital discharge. The home visit will occur within 7 days of hospital discharge and will consist of a complete hospital and medication review by a physician or nurse practitioner and a pharmacist (including all lab tests, imaging studies, medication changes, and proposed plan of care at the time of discharge). The investigators hypothesize these home visits will reduce 30 and 90 days hospital readmission rates and ED visits.
The number of emergency department visits and unplanned hospital readmissions will be tracked at 30 and 90 days following discharge from the hospitalization that led to study enrollment. A comparison cohort of patients discharged in the 12 months prior to study initiation will be used to compare the effectiveness of the home visit program. The number and type of adverse drug events (ADE) and potential adverse drug events (pADE) that occur during transitions of care will also be characterized. All ADE and pADE will be resolved during the initial home visit and will be classified based on severity. All ADE and pADE will be evaluated independently by two pharmacist reviewers; each reviewer will independently assign a severity rating to each ADE and pADE.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Contacts and Locations
Study Locations
-
-
Ohio
-
Columbus, Ohio, United States, 43221
- The Ohio State University Division of General Internal Medicine Martha Morehouse
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Adult patients discharged from the hospital in the last 7 days and with more than two chronic conditions and significant obstacles to accessing care in an office setting are eligible for study participation
Exclusion Criteria:
- Adult patients able to access care in an office setting.
- Adult patients discharged from the hospital greater than 7 days prior to the office visit.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Recently discharged homebound patients
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Hospital Readmission
Time Frame: 30 days
|
30 days
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Emergency Department Visit
Time Frame: 30 days
|
30 days
|
Other Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Number of drug related problems identified
Time Frame: 30 days
|
30 days
|
|
Type of drug related problems identified
Time Frame: 30 days
|
30 days
|
Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2013H0185
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Home Visits
-
Ghana Health ServicesUniversity of Warwick; Ellembelle District Health Directorate GhanaCompletedPregnant Women | Home VisitsGhana
-
serpil tokerBilimsel Araştirma Projeleri Birimi, Tokat Gaziosmapaşa ÜniversitesiCompletedPregnancy | Prenatal Care | Home VisitsTurkey
-
University of AlbertaCanadian Institutes of Health Research (CIHR)Not yet recruitingFamily | Dementia in Nursing Home | Remote Visits
-
State University of New York at BuffaloMedical University of South Carolina; University of Pennsylvania; University... and other collaboratorsRecruitingRemote Visits | In-person Visits | Remote vs. In-PersonUnited States
-
National Bureau of Economic Research, Inc.National Institute on Aging (NIA)CompletedParticipation in Nurse VisitsUnited States
-
Wake Forest University Health SciencesNational Institute on Minority Health and Health Disparities (NIMHD)CompletedWell-child Care VisitsUnited States
-
Universitat Internacional de CatalunyaCompletedDisruptive Global Behavior During Previous Treatment VisitsSpain
-
Sri Ramachandra Institute of Higher Education and...Completed
-
MetroHealth Medical CenterCleveland Metropolitan School District; Environmental Health Watch; Legal Aid...CompletedAsthma | Pediatric ALL | Medical Informatics | Social Determinants of Health | School Health Services | Registries | Home Visits | Housing Problems | Healthcare Disparity | Health Status DisparityUnited States
-
University GhentUniversiteit AntwerpenCompleted
Clinical Trials on Collaborative visit with provider and pharmacist
-
Brigham and Women's HospitalNational Institute on Aging (NIA); Wake Forest University Health SciencesNot yet recruitingHypertension | Primary Care
-
University of JordanCompletedPharmacist-Patient RelationsJordan
-
VA Office of Research and DevelopmentCompletedUrinary IncontinenceUnited States
-
Dartmouth-Hitchcock Medical CenterDartmouth College; National Center for Advancing Translational Sciences (NCATS)RecruitingAnxiety Disorders | Depression DisordersUnited States
-
University of PittsburghNational Institute on Alcohol Abuse and Alcoholism (NIAAA); Johns Hopkins UniversityRecruitingSexual Violence | Drinking HeavyUnited States
-
International Agency for Research on CancerCHU de Reims; Central Hospital, Nancy, France; Centre Régional de Coordination...Recruiting
-
Northwestern UniversityAllianceChicago; Cook County HealthActive, not recruitingGestational Diabetes Mellitus | Hypertension in Pregnancy | DysglycemiaUnited States
-
University of Illinois at ChicagoNational Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)Completed
-
Johns Hopkins UniversityPatient-Centered Outcomes Research Institute; National Heart, Lung, and Blood...CompletedUncontrolled HypertensionUnited States
-
The Leeds Teaching Hospitals NHS TrustUnknown