Clinical Utility of CDMT Among VillageMD Providers

Qure Healthcare

Status: Completed

Conditions: Medication Adherence; Chronic Disease; Drug Drug Interaction

Treatments: Other: Educational Materials for Chronic Disease Management Test (CDMT)

Study type: Interventional

Funder types: Industry

Identifiers

NCT05658653

Pro00064387

Details and patient eligibility

About

This is a health system-level research study of physicians and care providers. The purpose of this study is to assess the clinical evaluation and management (drug, procedures, counseling, and other) of a subset of common patient care indications.

Full description

The results of this study could contribute to improved quality of care for patients by encouraging better care practices and adherence to evidence-based guidelines. The data from this study will be submitted to a national journal for publication. The study plans to enroll up to 150 physicians.

Upon consenting and agreeing to participate in this study, participants will be asked to care for 3 simulated patient cases, known as Clinical Performance and Value Vignettes (CPV®). CPVs describe patients physicians typically encounter in their daily practice and are not meant to be difficult. In each vignette, physicians are asked to share their expected care through 5 domains: 1) history, 2) physical exam, 3) diagnostic workup, 4) diagnosis, and 5) treatment and follow-up. Each case takes approximately 15-20 minutes to complete and the investigators estimate the time commitment for each round of CPV administration to be approximately 45 - 60 minutes. All responses to the cases will be completed online and will be kept confidential. Over 2 CPV administration rounds, the total time to care for the simulated patients is estimated at 1.5-2 hours.

If physicians are randomized to the intervention group in this study, they will receive educational materials on a novel diagnostic test after the first round of CPV administration. They are asked to review these materials before moving to the next CPV administration round. The time to review educational materials is estimated to be approximately 15 minutes.

Depending on the results of this randomized controlled trial, there may be an opportunity for physicians to re-enroll in a follow-on study. If they choose to participate in this second study, they will be asked to identify and send de-identified records of patients in their practice that are similar to the simulated patients they previously cared for in this study.

Enrollment: 166 patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

• Licensed primary care provider (PCP) (MD, DO, NP, PA) currently practicing in the following areas: a) Internal medicine b) Family medicine
• Have practiced as a PCP in internal or family medicine for greater than 2 but less than 30 years
• practicing in a community / non-academic based practice setting
• ≥ 40 patients under care weekly
• Commonly treats patients with congestive heart failure/atrial fibrillation, diabetes, hypertension, and COPD
• Practicing in the United States
• English-speaking
• Access to the internet
• Informed and voluntarily consented to be in the study

Exclusion criteria

• Non-English speaking
• Not a licensed primary care provider
• Unable to access the internet
• Not practicing in the U.S.
• Do not voluntarily consent to be in the study

Trial design

Primary purpose: Diagnostic

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

---

166 participants in 2 patient groups

Standard Practice

No Intervention group

Description:

The Control group treats their simulated patients using standard practice and has no introduction to the new CDMT test.

Chronic Disease Management Test (CDMT)

Experimental group

Description:

The intervention will receive information regarding the CDMT test and will be given the test results, whether selected or not, in Round 2 of CPV administration.

Treatment:

Other: Educational Materials for Chronic Disease Management Test (CDMT)