Pre-screening to identify adults who may be eligible for future metabolic and mental health opportunities.
Official title: Pre-screening Survey for Metabolic, Cardiovascular, Obesity, Mental Health, and Endocrine Trial Eligibility (DOVE-MET-COME-100)
Run by Clindove Research LLC · NCT07106879 · Data updated 2026-11-12
This prescreening will see if adults with metabolic conditions or mental health disorders qualify for upcoming clinical opportunities by collecting health history, basic tests, and a doctor interview.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 7000 (estimated) |
| Sponsor | Clindove Research LLC Academic / other |
| Locations | 1 site (Brooklyn, New York) |
| Status | Recruiting |
| Started | July 30, 2025 |
| Main results expected | July 1, 2030 |
| Study ends | December 1, 2030 |
| Registry record updated | August 12, 2025 |
| Trial ID | NCT07106879 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults aged 18 and older with cardiovascular, metabolic, obesity-related, prediabetes, or mental health conditions who can give informed consent and comply with basic screening procedures are ideal candidates.
✕Probably not a fit
Pregnant or breastfeeding individuals, those with severe cognitive impairment or acute psychiatric emergencies, people with known drug or alcohol misuse, or those already enrolled in conflicting research are unlikely to benefit from this prescreening.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This single-site observational prescreening enrolls adults 18 and older to collect demographics, medical history, current symptoms, and basic health data including vital signs, urine drug screens, pregnancy tests when applicable, and blood samples. A physician oversees informed consent and conducts a one-on-one medical history review and eligibility interview. The study team may contact participants' current doctors or pharmacies to verify records when needed. No investigational treatments are given; data are used only to determine fit for future metabolic and psychiatric sub-studies.
Why it matters
Potential benefit: If successful, this program could help people find and be referred to relevant future clinical opportunities more quickly.
How similar studies have gone: Other prescreening registries and pre-enrollment approaches have been used successfully to speed recruitment and match patients to suitable studies, so this is a commonly used method.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Any participant of age 18 years and over * Who are willing to provide informed consent and participate in the pre-screening study and comply with study procedures. Exclusion Criteria: * Pregnant or breastfeeding individuals * Individuals having severe cognitive impairment or inability to provide informed consent * Individuals having acute psychiatric emergencies requiring immediate intervention/hospitalization * Individuals who are currently participating in another research study that conflicts with pre-screening data collection * Individuals having known history of drug/alcohol misuse * Individuals having medical conditions that, in the investigator's opinion, could compromise the integrity of the screening process or pose significant risks to the participant's health.
Where it's running
-
Clindove Research LLC
Brooklyn, New York, United States Recruiting
Study contacts
- Principal investigator: Nelly Cohen, MD — Clindove Research LLC
- Study coordinator: Nelly Cohen, MD
- Email: study@clindoveresearch.com
- Phone: 516-518-3239
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.