New test aims to improve doctor decisions for chronic illness
NCT ID NCT05192590
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at whether a new test (CDMT) helps primary care doctors make better decisions for patients with cardiometabolic syndrome. 247 board-certified physicians participated, with some using the test and others not. Researchers measured the quality of care and expected costs to see if the test improves patient management.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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247 people
The number who actually took part.
- Started
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Oct 2021
- Finished
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Feb 2023
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Subjects must meet the following criteria to be enrolled in the study: 1. Board-certified physician currently practicing in the following areas: 1. Internal medicine 2. Family medicine 2. Have practiced as a board-certified physician in internal or family medicine or greater than 2 but less than 30 years 3. Community / non-academic based practice setting 4. ≥ 40 patients under care weekly 5. Commonly treats patients with atrial fibrillation, coronary artery disease, congestive heart failure, diabetes, hypertension, and hyperlipidemia 6. Practicing in the U.S. 7. English-speaking 8. Access to the internet 9. Informed and voluntarily consented to be in the study Exclusion Criteria: 1. Non-English speaking 2. Practicing in an academic setting 3. Unable to access the internet 4. Not practicing in the U.S. 5. Do not voluntarily consent to be in the study
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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QURE Healthcare
San Francisco, California, 94109, United States
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Other studies related to the condition(s) this trial covers.
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