- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03355144
Resident Observed Burnout After Daily Supplementation With Coffee (ROBSTA)
May 21, 2018 updated by: NYU Langone Health
Coffee drinking is frequently reported as a negative outcome in studies on burnout, but the effect of an increased coffee intake on resident burnout has not been reported in the literature.
This study is a prospective, interventional cohort study enrolling up to 50 residents from the Internal Medicine Residency Program to look at the relationship between coffee and resident burnout.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Resident burnout is increasingly being recognized as detrimental to both physician well being and patient care.
It has been linked to an increased rate of medical errors and a reduced quality of patient care.
In addition, there have been multiple high-profile physician suicides in the past years.
This has resulted in a renewed focus on physician mental health and workload.
Study Type
Interventional
Enrollment (Actual)
39
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
New York
-
New York, New York, United States, 10016
- New York University School of Medicine
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 80 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- A resident in the NYU Internal Medicine residency program
Exclusion Criteria:
- Allergy or intolerance to coffee or caffeine
- Pregnancy
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Internal Medicine residents at NYU
effect of supplying Internal Medicine residents at NYU with free coffee on self reported features of psychological health, energy and burnout
|
At the beginning of study week 2 (study day 8), two coffee machines (one Nespresso Inissia and one Hamilton Beach 46205 12 Cup Programmable Coffee Maker) will be installed in the resident work rooms at each site. Subjects will be provided with free coffee beans, milk, cream, sugar and sweetener |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Self reported feelings of burnout
Time Frame: 1 Month
|
14 question survey measuring number of cups of coffee and level of exhaustion
|
1 Month
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Coffee consumption measured by self reporting questionaire
Time Frame: 1 Month
|
Measured by self reporting questionnaire
|
1 Month
|
Self reported emotional well being
Time Frame: 1 Month
|
14 question survey with questions measuring emotional wellbeing
|
1 Month
|
Self reported feelings of value
Time Frame: 1 Month
|
14 question survey with questions measuring feelings of self value
|
1 Month
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Steven Liu, MD, NYU Langone Health
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 Major Dates
Study Start (Actual)
March 22, 2018
Primary Completion (Actual)
April 12, 2018
Study Completion (Actual)
April 12, 2018
Study Registration Dates
First Submitted
November 22, 2017
First Submitted That Met QC Criteria
November 22, 2017
First Posted (Actual)
November 28, 2017
Study Record Updates
Last Update Posted (Actual)
May 22, 2018
Last Update Submitted That Met QC Criteria
May 21, 2018
Last Verified
May 1, 2018
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 17-01011
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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.
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