Engineering Whole Health Into Hospital Care - University of Michigan
NCT ID: NCT07215117
Last Updated: 2025-11-12
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
300 participants
INTERVENTIONAL
2025-09-10
2026-03-31
Brief Summary
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Detailed Description
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The goal of this study is to implement and evaluate an inpatient Whole Health Bundle intervention to improve hospitalized patients' well-being. This study will assess if implementing an Inpatient Whole Health Bundle is associated with improved patient-centric outcomes (such as perceptions of the healing environment and patient satisfaction) among hospitalized patients.
This is a quasi-experimental pre-test/post-test trial. The study will be conducted at one medical unit at the University of Michigan hospital. Study subjects will be hospitalized patients. The study will be conducted in 2 phases- pre-intervention and intervention. Each study phase will last 1-2-months. During the pre-intervention phase, a sample of patients recently discharged from the hospital will be mailed a study survey. The survey will ask questions about their satisfaction with their hospital stay.
During the intervention phase, patients staying in the hospital will be asked if they would like to participate in the study. Participants will be offered a menu of items and services that could help improve their overall well-being and their hospital stay. Patient will be free to choose or decline any of the items on the menu. A researcher will record which items, if any, a patient selects. Patients in the intervention will be mailed the same study survey as the pre- intervention phase after they are discharged from the hospital. Researchers will compare patient satisfaction responses between patients staying in the hospital during the pre- intervention phase to those who participated in the intervention. A few patients will be asked to participate in a study interview. The interviews are to better understand intervention experiences as well as barriers and facilitators to improving patient satisfaction with their hospital stay. In addition, unit level metrics will be assessed between the pre-intervention and intervention time periods.
Conditions
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Keywords
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Study Design
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NON_RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
NONE
Study Groups
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Whole Health Intervention Participants
Hospitalized patients on the intervention units will be offered participation in the Inpatient Whole Health Bundle.
Inpatient Whole Health Bundle
Hospitalized patients on the intervention units will be offered participation in the Inpatient Whole Health Bundle, which is comprised of a variety of offerings aimed at improving the wellbeing of the patient. They can choose to use any or none of the bundle elements.
Pre-Intervention Participants
Randomly selected patients who had been discharged within the 1-2 months prior to the intervention will be recruited to provide information via a survey.
No interventions assigned to this group
Interventions
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Inpatient Whole Health Bundle
Hospitalized patients on the intervention units will be offered participation in the Inpatient Whole Health Bundle, which is comprised of a variety of offerings aimed at improving the wellbeing of the patient. They can choose to use any or none of the bundle elements.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* patients that are cognitively impaired or unable to provide their own consent
* patients that are under respiratory contact precautions.
18 Years
ALL
No
Sponsors
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University of Michigan
OTHER
Responsible Party
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Sanjay Saint
Professor of Internal Medicine
Principal Investigators
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Sanjay Saint, MD, MPH
Role: PRINCIPAL_INVESTIGATOR
University of Michigan
Locations
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University of Michigan
Ann Arbor, Michigan, United States
Countries
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Central Contacts
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Facility Contacts
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Karen Fowler, MPH
Role: primary
Other Identifiers
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HUM00270511
Identifier Type: -
Identifier Source: org_study_id