RECRUITING

This Pre-screening Protocol Aims to Evaluate Participants for Potential Trial Eligibility in Future Clindove Research Studies Focusing on Metabolic and Psychiatric Health. It Involves Non-interventional Screening Activities to Assess Eligibility for Future Clinical Trials.

Description

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.

Study Overview

Study Details

Study 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.

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

This Pre-screening Protocol Aims to Evaluate Participants for Potential Trial Eligibility in Future Clindove Research Studies Focusing on Metabolic and Psychiatric Health. It Involves Non-interventional Screening Activities to Assess Eligibility for Future Clinical Trials.

Condition
Cardiovascular Diseases
Intervention / Treatment

-

Contacts and Locations

Brooklyn

Clindove Research LLC, Brooklyn, New York, United States, 11221

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility 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.
  • * 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.

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

Yes

Collaborators and Investigators

Clindove Research LLC,

Study Record Dates

2030-12-01