Bonding Bundle for Physician-Patient Relationships
Trial Summary
Will I have to stop taking my current medications?
The trial information does not specify whether patients need to stop taking their current medications.
What data supports the effectiveness of the M-Well Bonding Bundle treatment?
The research on patient education and provider engagement, such as the myJointReplacement.ca project, shows that integrating patient and provider perspectives can improve knowledge and practice alignment, which may suggest that similar approaches in the M-Well Bonding Bundle could enhance physician-patient relationships.12345
What is the purpose of this trial?
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.
Research Team
Sanjay Saint, MD
Principal Investigator
University of Michigan
Eligibility Criteria
This trial is for attending physicians treating hospitalized medical patients and their adult patients who can consent. It excludes surgical attendings, residents, those with cognitive impairments, or non-English speakers.Inclusion Criteria
Exclusion Criteria
Timeline
Screening
Participants are screened for eligibility to participate in the trial
Intervention
Doctors in the intervention arm use suggested strategies to improve interactions with patients during their 2-week work rotation.
Control
Doctors in the control arm conduct rounds as usual without using intervention strategies.
Follow-up
Participants are monitored for the effectiveness of the intervention through surveys and interviews.
Treatment Details
Interventions
- M-Well Bonding Bundle
Find a Clinic Near You
Who Is Running the Clinical Trial?
University of Michigan
Lead Sponsor
Agency for Healthcare Research and Quality (AHRQ)
Collaborator