M-Well Bonding Bundle to Improve Patient-Physician Relationships
The goal of this clinical trial is to learn more about the interaction between a patient in the hospital and their treating doctor. A good relationship between patients and their doctors can help improve patient care. Doctors will be asked to use strategies to improve their interactions with patients in the hospital. The main questions it aims to answer are: * Will using the intervention strategies improve doctors' empathy towards their patients? * Will using the intervention strategies lead to improved scores in patient views of doctors' empathy? There will be 2 study arms. One group of doctors will be asked to use the intervention strategies. The other group of doctors will provide care as they would normally. Researchers will compare the doctors in the intervention arm to those in the control arm. Doctors are the primary subjects for this study. The doctors in both study arms will be asked to do the following: 1. Allow study staff to observe the interaction between them and their patients. 2. Complete a brief survey at the end of their 2-week work rotation. Doctors who are in the intervention arm will be asked to use suggested strategies when visiting with patients in the hospital. Patients are secondary subjects for this study. Patients of participating doctors may be asked to do the following: 1. Allow study staff to observe the interaction between them and their doctors. 2. Complete a brief survey after meeting with their doctor.
Conditions:
Physician-Patient Relations
Study Start (Actual) 2024-04-08
Primary Completion (Estimated) 2026-06
Study Completion (Estimated) 2026-06
Enrollment (Estimated) 3624
Study Type INTERVENTIONAL
Phase NA
Locations:
📍 Ann Arbor, Michigan, United States
📍 Ann Arbor, Michigan, United States

Eligibility Criteria

Description

  • Primary Subjects - Physicians
  • Inclusion Criteria:

    • * Attending physicians caring for hospitalized medical patients

    Exclusion Criteria:

    • * Surgical attendings
    • * Residents
    • Secondary Subjects - Patients
    • Inclusion Criteria
    • * Hospitalized adult patient
    • * Patient of an enrolled physician in the study
    • * Cognitively impaired
    • * Unable to provide informed consent
    • * Does not speak English
Ages Eligible for Study: 18 Years to N/A (ADULT, OLDER_ADULT)
Sexes Eligible for Study: ALL
Accepts Healthy Volunteers: No

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

  • First Submitted2024-04-03
  • First Submitted that Met QC Criteria2024-04-03
  • First Posted2024-04-09

Study Record Updates

  • Last Update Submitted that Met QC Criteria2024-04-08
  • Last Update Posted2024-04-10
  • Last Verified2024-04