Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT07166913

Enhancing Engagement of Partners in Research

Led by NYU Langone Health · Updated on 2025-09-16

480

Participants Needed

1

Research Sites

64 weeks

Total Duration

On this page

Sponsors

N

NYU Langone Health

Lead Sponsor

P

Patient-Centered Outcomes Research Institute

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Enhancing Engagement of Partners in Research

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Principal investigators must oversee a study that has not started enrollment or is within 1-3 months of starting enrollment and is within 25% of the recruitment target.
  • Studies that have started enrollment must be no further than 25% of the projected enrollment timeline with at least 6 months remaining.
  • The study must aim to recruit more than 50 participants.
  • The study must include at least 10 stakeholder partners.
  • Principal investigators must be 18 years or older.
  • Stakeholders must be 12 years or older.
  • Stakeholders must be able to speak English, Spanish, or Chinese.
  • Stakeholders must be part of the study team or serve in an advisory capacity.
  • Key informants must meet the same criteria as stakeholders and principal investigators.
Not Eligible

You will not qualify if you...

  • Individuals unable to complete the 6-month follow-up assessment.
  • Children who are wards or foster children.
  • Individuals unable or unwilling to provide consent.
  • Individuals concurrently enrolled in another study within this research project.
  • Principal investigators with extensive experience in stakeholder engagement based on a screener survey.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

NYU Langone Health

New York, New York, United States, 10016

Actively Recruiting

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Research Team

H

H. Shonna Yin, MD, MS

CONTACT

J

Jessica Velazquez-Perez

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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