RECRUITING

Enhancing Engagement of Partners in Research

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

The purpose of this study is to examine the implementation and effectiveness of a bundle of engagement strategies for pediatric patient centered outcomes research (PCOR) studies. The study aims to examine the effectiveness of a "bundle" of enhanced engagement strategies on improved stakeholder engagement and study protocol indicators (including improved language access, meeting recruitment/retention goals) compared to standard practice.

Official Title

Enhancing Stakeholder Engagement in Pediatric Research

Quick Facts

Study Start:2025-09-08
Study Completion:2026-12-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT07166913

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. 1. Studies who either have not started enrollment or are within 1-3 months of the start of enrollment, and within the 25% ceiling for % recruitment target.
  2. 2. Studies that have started enrollment must be no further than 25% of projected enrollment timeline of the study (with at least 6 months remaining for enrollment).
  3. 3. Target n\>50 participants in study.
  4. 4. At least 10 stakeholder partners part of study. The PI's must also be ≥18 years old;
  5. 1. \>=12 years old;
  6. 2. Ability to speak either English, Spanish, or Chinese, and;
  7. 3. Part of the study team or serving in an advisory capacity to the study team
  1. 1. Not able to complete 6 month follow-up assessment
  2. 2. Children who are wards/foster children
  3. 3. Not able or willing to provide consent.
  4. 4. Concurrent enrollment in another study that is part of this research project.

Contacts and Locations

Study Contact

H. Shonna Yin, MD, MS
CONTACT
646-501-4284
Hsiang.Yin@nyulangone.org
Jessica Velazquez-Perez
CONTACT
646-501-4288
Jessica.velazquez@nyulangone.org

Principal Investigator

H. Shonna Yin, MD, MS
PRINCIPAL_INVESTIGATOR
NYU Langone Health

Study Locations (Sites)

NYU Langone Health
New York, New York, 10016
United States

Collaborators and Investigators

Sponsor: NYU Langone Health

  • H. Shonna Yin, MD, MS, PRINCIPAL_INVESTIGATOR, NYU Langone Health

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 Date2025-09-08
Study Completion Date2026-12-01

Study Record Updates

Study Start Date2025-09-08
Study Completion Date2026-12-01

Terms related to this study

Additional Relevant MeSH Terms

  • Stakeholder Engagement