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.

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

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.

Official Title

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

Quick Facts

Study Start:2025-07-30
Study Completion:2030-12-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT07106879

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.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Any participant of age 18 years and over
  2. * Who are willing to provide informed consent and participate in the pre-screening study and comply with study procedures.
  1. * Pregnant or breastfeeding individuals
  2. * Individuals having severe cognitive impairment or inability to provide informed consent
  3. * Individuals having acute psychiatric emergencies requiring immediate intervention/hospitalization
  4. * Individuals who are currently participating in another research study that conflicts with pre-screening data collection
  5. * Individuals having known history of drug/alcohol misuse
  6. * 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.

Contacts and Locations

Study Contact

Nelly Cohen, MD
CONTACT
516-518-3239
team@clindoveresearch.com
Ian Ho, Site Director
CONTACT
516-512-4122
ian@clindoveresearch.com

Study Locations (Sites)

Clindove Research LLC
Brooklyn, New York, 11221
United States

Collaborators and Investigators

Sponsor: Clindove Research LLC

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-07-30
Study Completion Date2030-12-01

Study Record Updates

Study Start Date2025-07-30
Study Completion Date2030-12-01

Terms related to this study

Additional Relevant MeSH Terms

  • Cardiovascular Diseases
  • Metabolic Syndrome
  • Obesity
  • Type 2 Diabetes Mellitus (T2D) and Chronic Kidney Disease (CKD)
  • Prediabetes
  • Mental Health Disorders
  • Endocrine Dysfunction
  • Chronic Kidney Diseases