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Quality IQ Patient Simulation Physician Practice Measurement and Engagement (Q-IQ)

Primary Purpose

Diabetes, Hypertension, Depression

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Continuing Medical Education
Quality IQ Patient Simulations
Sponsored by
Qure Healthcare, LLC
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Diabetes

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. Board-certified in internal medicine or family medicine
  2. Minimum patient panel size of 1,500 patients
  3. English-speaking
  4. Access to the internet
  5. Informed, signed and voluntarily consented to be in the study

Exclusion Criteria:

  1. Not board certified in either internal medicine or family medicine
  2. Patient panel size less than 1,500 patients
  3. Non-English speaking
  4. Unable to access the internet
  5. Does not voluntarily consent to be in the study

Sites / Locations

  • QURE Healthcare

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Control

CME

Arm Description

The Control arm will be asked to care for online, Quality IQ patient simulations and will receive feedback based on their care decisions made in each case. The feedback will identify correct care, unneeded care, or gaps in care and recommend or reinforce evidence-based care decisions and includes references. This arm will not be offered Continuing Medical Education (CME) or American Board of Internal Medicine (ABIM) Part II Maintenance of Certification (MOC) credits for their participation.

The CME arm will be asked to care for online, Quality IQ patient simulations and will receive feedback based on their care decisions made in each case. The feedback will identify correct care, unneeded care, or gaps in care and recommend or reinforce evidence-based care decisions and includes references. This arm will be offered Continuing Medical Education (CME) and American Board of Internal Medicine (ABIM) Part II Maintenance of Certification (MOC) credits for their participation.

Outcomes

Primary Outcome Measures

Change in the percentage of evidence-based diagnostic and treatment decisions made in the simulations.
In each case, participants will answer multiple-choice questions about their preferred course of action to work-up, diagnose and treat patients in the primary care setting. Each question has specific evidence-based scoring criteria identifying necessary and unnecessary care decisions. Each provider will get a score for each case, ranging from 0 to 100 percentage based on the care decisions they make in the case. Over the course of the project, the investigators will track the percentage of correct, evidence-based care decisions made by participants, with the hypothesis that serial measurement and feedback on evidence-based care decisions will lead to increases in appropriate decisions over time. Higher scores represent a better outcome.

Secondary Outcome Measures

Change in MIPS-relevant care decisions made in the patient simulations
As described in the primary outcome measure, the investigators will track the percentage of evidence-based care decisions made by participants in the patient simulations. A subset of these care decisions tie directly to quality measures tracked by Medicare through the Merit-based Incentive Payment System (MIPS). For this outcome measure, the investigators will track changes in the percentage of MIPS-relevant work-up and treatment decisions made in the patient simulations. Higher scores represent a better outcome.
Change in ordering of unneeded work-up tests made in the patient simulations
As described in the primary outcome measure, the investigators will track the percentage of evidence-based care decisions made by participants in the patient simulations. A subset of these care decisions tie to ordering of unneeded laboratory and imaging testing that is not supported by the evidence-based guidelines. For this outcome measure, the investigators will track changes in the frequency with which unneeded tests are ordered in the patient simulations. Higher scores represent a better outcome.
Participant case completion rate
The investigators will track the percentage of enrolled participants who stay engaged in the study and complete at least 75% of their patient simulation cases.
Participant Satisfaction
Investigators will measure participant satisfaction as measured by post-evaluation survey. On a scale of 1 to 5 (with 5 being the highest), participants will be asked about the overall quality of the material, the relevance to their practice and the educational content. Higher scores represent a better outcome.
Impact of available CME and ABIM MOC on recruitment rate
Operating under the hypothesis that physicians offered CME and MOC credits are more likely to participate in a quality improvement program like this, the investigators will track the rate at which a randomized group of primary care physicians enroll in the program when offered CME and MOC credit and compare that to a group that is not offered CME and MOC credit for their participation.
Impact of available CME and ABIM MOC on retention rate
Operating under the hypothesis that physicians offered CME and MOC credits are more likely to continue participating in a quality improvement program, the investigators will track the rate at which a primary care physicians eligible to earn CME and MOC credit complete the full 8 week project and compare that to a group that is not offered CME and MOC credit.

Full Information

First Posted
January 4, 2019
Last Updated
March 2, 2020
Sponsor
Qure Healthcare, LLC
Collaborators
CE Outcomes
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1. Study Identification

Unique Protocol Identification Number
NCT03800901
Brief Title
Quality IQ Patient Simulation Physician Practice Measurement and Engagement
Acronym
Q-IQ
Official Title
Quality IQ Patient Simulation Physician Practice Measurement and Engagement
Study Type
Interventional

2. Study Status

Record Verification Date
March 2020
Overall Recruitment Status
Completed
Study Start Date
January 11, 2019 (Actual)
Primary Completion Date
March 11, 2019 (Actual)
Study Completion Date
April 15, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Qure Healthcare, LLC
Collaborators
CE Outcomes

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This study will test the quality of physician care decisions using a patient-simulation based measurement and feedback approach that combines multiple-choice care decisions with real-time, personalized scoring and feedback. The study will also measure the impact of gaming-inspired competition and motivation, including a weekly leaderboard, to improve evidence-based care decisions. In addition, the study the test the impact of CME and MOC credits on participant engagement in the process.
Detailed Description
Primary care providers (PCPs) make many of the most important care decisions, especially for patients with chronic conditions and multiple co-morbidities. Studies have confirmed that unwarranted variation is common among PCPs, with high level of variation in care documented between urban and rural practices, across regions, and even among providers within a single healthcare system. The investigators' previous work has shown that patient simulations can rapidly and reliably measure unwarranted practice variation among providers. In addition, published work shows that patient simulations, when administered serially and combined with customized feedback on improvement opportunities can reduce practice variation and improve performance on patient-level quality measures. Given the large scope of unwarranted variation in medical practice, there is a need for scalable approaches to measure care decisions, provide feedback on improvement opportunities and benchmark performance to peers. This study seeks to evaluate the impact of measurement, feedback and competition on evidence-based care decisions made by primary care providers across the country. It is a randomized, controlled trial with multiple measurements across key domains of clinical care. All participants are asked to care for simulated patients designed to look like typical patients seen in a primary care practice. In each case, providers will answer multiple-choice questions about their preferred course of action to work-up, diagnose and treat patients in the primary care setting. After each question, providers will receive evidence-based feedback, including references, on the appropriateness of each of their care decisions. Feedback will be supported with relevant reference to evidence-based guidelines, including national MIPS quality measures. All participants will receive the following interventions: Feedback on care decisions made in each Quality IQ case, which will identify correct care, unneeded care, or gaps in care. This feedback will recommend or reinforce evidence-based care decisions and includes references. All cases will be scored against evidence-based criteria. For each case, providers will start with 100 base points. Correct care decisions will add to that total, while unnecessary care decisions will subtract from that total. A weekly leaderboard will be posted online, allowing participants to see how they are performing relative to their peers across the country. Participants will have the opportunity to select a unique username or an anonymous user ID to be identified on the leaderboard, to maintain anonymity. Half of the recruits will be offered Category I CME credit approved by The University of California, San Francisco School of Medicine (UCSF) which has been accredited by the Accreditation Council of Continuing Medical Education to provide CME for physicians and MOC points in the ABIM's MOC program.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes, Hypertension, Depression, Osteoarthritis, Asthma, Pain, Heart Failure

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The study will enroll practicing PCPs in the US. Once eligibility is determined and providers are enrolled in the study, they will be randomized into one of two arms: Control: will not be offered CME or ABIM MOC credits for their participation. CME Arm: will be offered CME or ABIM MOC credits for their participation. Between the two arms, all other aspects of the study will remain constant. All providers will then care for 1 Quality IQ patient simulation each week over the course of 6-8 weeks.
Masking
Participant
Masking Description
The Control arm, who are not offered CME or ABIM MOC credits for their participation, will be unaware of the interventional CME arm. The CME arm will also be unaware of the Control arm. Per recommendations from the IRB, all participants at the end of the study will receive a study debrief letter informing them of the other study arms.
Allocation
Randomized
Enrollment
187 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control
Arm Type
Active Comparator
Arm Description
The Control arm will be asked to care for online, Quality IQ patient simulations and will receive feedback based on their care decisions made in each case. The feedback will identify correct care, unneeded care, or gaps in care and recommend or reinforce evidence-based care decisions and includes references. This arm will not be offered Continuing Medical Education (CME) or American Board of Internal Medicine (ABIM) Part II Maintenance of Certification (MOC) credits for their participation.
Arm Title
CME
Arm Type
Experimental
Arm Description
The CME arm will be asked to care for online, Quality IQ patient simulations and will receive feedback based on their care decisions made in each case. The feedback will identify correct care, unneeded care, or gaps in care and recommend or reinforce evidence-based care decisions and includes references. This arm will be offered Continuing Medical Education (CME) and American Board of Internal Medicine (ABIM) Part II Maintenance of Certification (MOC) credits for their participation.
Intervention Type
Other
Intervention Name(s)
Continuing Medical Education
Other Intervention Name(s)
CME
Intervention Description
CME or ABIM MOC credits
Intervention Type
Other
Intervention Name(s)
Quality IQ Patient Simulations
Other Intervention Name(s)
Clinical Performance and Value vignettes, CPVs
Intervention Description
Online patient cases designed to simulate typical patients seen in a primary care practice. In each case, providers will answer multiple-choice questions about their preferred course of action to work-up, diagnose and treat patients in the primary care setting. After each question, providers will receive evidence-based feedback, including references, on the appropriateness of each of their care decisions. Feedback will be supported with relevant reference to evidence-based guidelines, including national MIPS quality measures. Cases will cover clinical conditions aligned with MIPS measures that are commonly seen in the primary care setting including: diabetes, hypertension, depression, osteoarthritis, asthma and pain control.
Primary Outcome Measure Information:
Title
Change in the percentage of evidence-based diagnostic and treatment decisions made in the simulations.
Description
In each case, participants will answer multiple-choice questions about their preferred course of action to work-up, diagnose and treat patients in the primary care setting. Each question has specific evidence-based scoring criteria identifying necessary and unnecessary care decisions. Each provider will get a score for each case, ranging from 0 to 100 percentage based on the care decisions they make in the case. Over the course of the project, the investigators will track the percentage of correct, evidence-based care decisions made by participants, with the hypothesis that serial measurement and feedback on evidence-based care decisions will lead to increases in appropriate decisions over time. Higher scores represent a better outcome.
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Change in MIPS-relevant care decisions made in the patient simulations
Description
As described in the primary outcome measure, the investigators will track the percentage of evidence-based care decisions made by participants in the patient simulations. A subset of these care decisions tie directly to quality measures tracked by Medicare through the Merit-based Incentive Payment System (MIPS). For this outcome measure, the investigators will track changes in the percentage of MIPS-relevant work-up and treatment decisions made in the patient simulations. Higher scores represent a better outcome.
Time Frame
3 months
Title
Change in ordering of unneeded work-up tests made in the patient simulations
Description
As described in the primary outcome measure, the investigators will track the percentage of evidence-based care decisions made by participants in the patient simulations. A subset of these care decisions tie to ordering of unneeded laboratory and imaging testing that is not supported by the evidence-based guidelines. For this outcome measure, the investigators will track changes in the frequency with which unneeded tests are ordered in the patient simulations. Higher scores represent a better outcome.
Time Frame
3 months
Title
Participant case completion rate
Description
The investigators will track the percentage of enrolled participants who stay engaged in the study and complete at least 75% of their patient simulation cases.
Time Frame
3 months
Title
Participant Satisfaction
Description
Investigators will measure participant satisfaction as measured by post-evaluation survey. On a scale of 1 to 5 (with 5 being the highest), participants will be asked about the overall quality of the material, the relevance to their practice and the educational content. Higher scores represent a better outcome.
Time Frame
3 months
Title
Impact of available CME and ABIM MOC on recruitment rate
Description
Operating under the hypothesis that physicians offered CME and MOC credits are more likely to participate in a quality improvement program like this, the investigators will track the rate at which a randomized group of primary care physicians enroll in the program when offered CME and MOC credit and compare that to a group that is not offered CME and MOC credit for their participation.
Time Frame
3 months
Title
Impact of available CME and ABIM MOC on retention rate
Description
Operating under the hypothesis that physicians offered CME and MOC credits are more likely to continue participating in a quality improvement program, the investigators will track the rate at which a primary care physicians eligible to earn CME and MOC credit complete the full 8 week project and compare that to a group that is not offered CME and MOC credit.
Time Frame
3 months

10. Eligibility

Sex
All
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Board-certified in internal medicine or family medicine Minimum patient panel size of 1,500 patients English-speaking Access to the internet Informed, signed and voluntarily consented to be in the study Exclusion Criteria: Not board certified in either internal medicine or family medicine Patient panel size less than 1,500 patients Non-English speaking Unable to access the internet Does not voluntarily consent to be in the study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
John Peabody, MD, PhD
Organizational Affiliation
QURE Healthcare
Official's Role
Principal Investigator
Facility Information:
Facility Name
QURE Healthcare
City
San Francisco
State/Province
California
ZIP/Postal Code
94109
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
No individual participant data will be shared with other researchers. Analysis will be conducted at the aggregate group level.
Citations:
PubMed Identifier
30328782
Citation
Burgon TB, Cox-Chapman J, Czarnecki C, Kropp R, Guerriere R, Paculdo D, Peabody JW. Engaging Primary Care Providers to Reduce Unwanted Clinical Variation and Support ACO Cost and Quality Goals: A Unique Provider-Payer Collaboration. Popul Health Manag. 2019 Aug;22(4):321-329. doi: 10.1089/pop.2018.0111. Epub 2018 Oct 17.
Results Reference
background
PubMed Identifier
26376210
Citation
Weigel PA, Ullrich F, Shane DM, Mueller KJ. Variation in Primary Care Service Patterns by Rural-Urban Location. J Rural Health. 2016 Spring;32(2):196-203. doi: 10.1111/jrh.12146. Epub 2015 Sep 16.
Results Reference
background
PubMed Identifier
10755498
Citation
Peabody JW, Luck J, Glassman P, Dresselhaus TR, Lee M. Comparison of vignettes, standardized patients, and chart abstraction: a prospective validation study of 3 methods for measuring quality. JAMA. 2000 Apr 5;283(13):1715-22. doi: 10.1001/jama.283.13.1715.
Results Reference
background
PubMed Identifier
15545677
Citation
Peabody JW, Luck J, Glassman P, Jain S, Hansen J, Spell M, Lee M. Measuring the quality of physician practice by using clinical vignettes: a prospective validation study. Ann Intern Med. 2004 Nov 16;141(10):771-80. doi: 10.7326/0003-4819-141-10-200411160-00008.
Results Reference
background
PubMed Identifier
34941547
Citation
Burgon T, Casebeer L, Aasen H, Valdenor C, Tamondong-Lachica D, de Belen E, Paculdo D, Peabody J. Measuring and Improving Evidence-Based Patient Care Using a Web-Based Gamified Approach in Primary Care (QualityIQ): Randomized Controlled Trial. J Med Internet Res. 2021 Dec 23;23(12):e31042. doi: 10.2196/31042.
Results Reference
derived

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Quality IQ Patient Simulation Physician Practice Measurement and Engagement

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