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

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

Recruiting
18 years and older
All
Phase N/A

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Overview

DOVE-MET-COME-100 is a single site prescreening survey study designed to identify adults who may be eligible for future industry-sponsored clinical trials. A physician will oversee the informed consent process, after which participants will be surveyed on demographics, medical history, current health conditions and symptoms. The study team may also collect basic health information, including vital signs, urine drug tests, blood samples and pregnancy tests (if applicable). A physician will review each participant's medical history in a one-on-one interview to assess potential fit for upcoming trials. If needed, the doctor may contact the participant's current doctors or pharmacies to gather more information for eligibility review.

Description

Eligible participants will undergo screening procedures including laboratory assessments and health questionnaires to determine their suitability for further evaluation in metabolic and/or psychiatric sub-studies. The study does not include any investigational intervention.

Eligibility

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.

Study details
    Cardiovascular Diseases
    Metabolic Syndrome
    Obesity
    Prediabetes
    Mental Health Disorders
    Endocrine Dysfunction
    Type 2 Diabetes Mellitus (T2DM)
    Chronic Kidney Disease (CKD)

NCT07106879

Clindove Research LLC

13 August 2025

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FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

Do I get compensated for taking part in clinical trials?

Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

How safe are clinical trials?

Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
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