ClinicalTrials.Veeva

Menu

Engineering Whole Health Into Hospital Care - University of Michigan

University of Michigan logo

University of Michigan

Status

Enrolling

Conditions

Whole Health

Treatments

Behavioral: Inpatient Whole Health Bundle

Study type

Interventional

Funder types

Other

Identifiers

NCT07215117
HUM00270511
1R18HS028963-01 (U.S. AHRQ Grant/Contract)

Details and patient eligibility

About

The purpose of this study is to test an intervention focused on improving patients' wellness and satisfaction with their hospital stay. As part of this study, patients hospitalized on specific hospital units will be asked to participate in the study intervention. This will help the researchers learn if the items offered will help improve patients' satisfaction with their hospital stay.

Full description

Whole Health is a model designed to address multiple patient needs. This includes physical and spiritual wellness, personal surroundings, nutrition, relationships, and mental wellness. The Whole Health approach focuses on improving overall patient wellness and includes increased availability of complementary and alternative medicine services. While some Whole Health work is being done at outpatient facilities, this study seeks to expand and test this approach to the inpatient setting, given the potential Whole Health has for addressing patient wellness.

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.

Enrollment

300 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • hospitalized patients on medical and medical/surgical units at the University of Michigan Health System

Exclusion criteria

  • patients that cannot speak English
  • patients that are cognitively impaired or unable to provide their own consent
  • patients that are under respiratory contact precautions.

Trial design

Primary purpose

Supportive Care

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

300 participants in 2 patient groups

Pre-Intervention Participants
No Intervention group
Description:
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.
Whole Health Intervention Participants
Experimental group
Description:
Hospitalized patients on the intervention units will be offered participation in the Inpatient Whole Health Bundle.
Treatment:
Behavioral: Inpatient Whole Health Bundle

Trial contacts and locations

1

Loading...

Central trial contact

Latoya Kuhn, MPH; Karen Fowler, MPH

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems