Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
ID07106879

Pre-screening Survey for Metabolic, Cardiovascular, Obesity, Mental Health, and Endocrine Trial Eligibility (DOVE-MET-COME-100)

Led by Clindove Research LLC · Updated on 2025-08-12

7000

Participants Needed

1

Research Sites

21 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are conducting a prescreening survey study called DOVE-MET-COME-100 to identify adults who may qualify for future clinical trials focused on metabolic, cardiovascular, obesity, mental health, and endocrine conditions. This observational study aims to collect detailed health and demographic information without testing any investigational treatments. The goal is to build a structured database of individuals with metabolic, cardiovascular, endocrine, and psychiatric risk factors to support upcoming industry-sponsored trials. Participants will undergo screening procedures including health questionnaires and laboratory tests such as blood work for metabolic and biomarker analysis, including Hemoglobin A1c, lipid panel, and liver and kidney function tests. There are no treatment interventions in this study; instead, participants will be evaluated for potential eligibility in future sub-studies through clinical evaluations and medical history reviews conducted by a physician. During the study, participants will provide informed consent and complete surveys on demographics, medical history, current health conditions, and symptoms. Basic health information such as vital signs, urine drug tests, blood samples, and pregnancy tests (if applicable) will be collected. A physician will review the medical history and may contact the participant's current doctors or pharmacies to gather additional information. The main measure of interest is the number of participants who express interest in future clinical research over five years while maintaining a detailed database of pre-screened individuals. The study is expected to last up to five years.

CONDITIONS

Brief Title

Non-interventional Pre-screening Protocol Aims to Evaluate Participants for Potential Trial Eligibility in Future Clinical Trials/Studies Focusing on Metabolic and Psychiatric Health.

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Participants aged 18 years and older
  • Willingness to provide informed consent and participate in the pre-screening study
  • Ability to comply with study procedures
Not Eligible

You will not qualify if you...

  • Pregnant or breastfeeding individuals
  • Severe cognitive impairment or inability to provide informed consent
  • Acute psychiatric emergencies requiring immediate intervention or hospitalization
  • Current participation in another conflicting research study
  • Known history of drug or alcohol misuse
  • Medical conditions that could compromise the screening process or pose significant health risks as judged by the investigator

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Trial Site Locations

Total: 1 location

1

Clindove Research LLC

Brooklyn, New York, United States, 11221

Actively Recruiting

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Research Team

N

Nelly Cohen, MD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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