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Enhancing Engagement of Partners in Research

Enhancing Stakeholder Engagement in Pediatric Research

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07166913
Enrollment
480
Registered
2025-09-11
Start date
2025-09-08
Completion date
2027-12-01
Last updated
2026-07-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stakeholder Engagement

Brief summary

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.

Interventions

BEHAVIORALToolkit

The toolkit contains information regarding enhanced stakeholder engagement strategies. The toolkit includes guidance materials, checklists, and templates/ sample materials, to increase stakeholder engagement in the research. This includes guidance on setting up a stakeholder advisory board (SAB) and ensuring literacy- and language- sensitivity of participant-/stakeholder-facing materials.

Sponsors

NYU Langone Health
Lead SponsorOTHER
Patient-Centered Outcomes Research Institute
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

In order to be eligible to participate in this study, PIs must oversee a study that meets the following criteria: 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. 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. Target n\>50 participants in study. 4. At least 10 stakeholder partners part of study. The PI's must also be ≥18 years old; In order for study stakeholders to be eligible to participate in this study, an individual must meet all of the following criteria: 1. \>=12 years old; 2. Ability to speak either English, Spanish, or Chinese, and; 3. Part of the study team or serving in an advisory capacity to the study team The same criteria as that used for stakeholder and PI eligibility applies to Key informant (KI) interviews.

Exclusion criteria

An individual who meets any of the following criteria will be excluded from participation in this study: 1. Not able to complete 6 month follow-up assessment 2. Children who are wards/foster children 3. Not able or willing to provide consent. 4. Concurrent enrollment in another study that is part of this research project. In addition, PI's who meet the following criteria will be excluded from participation in this study: 1\. A lot of experience with stakeholder engagement (based on screener survey question)

Design outcomes

Primary

MeasureTime frameDescription
Research Engagement Survey Tool (REST) stakeholder engagement scoreMonth 6This tool consists of 32 items and assesses engagement across 8 domains, using a 5-point Likert scale for each item. The 8 domains include: 1) focus on community perspectives and determinants of health, 2) partner input, 3) partnership sustainability, 4) fostering co-learning, capacity building and co-benefit, 5) building on strengths and resources, 6) facilitating collaborative, equitable partnerships, 7) involving partners in the dissemination process, and 8) building and maintaining trust. Engagement principle (EP) scores are calculated as an average of non-missing items. The 8 means are used to calculate the overall stakeholder engagement score. Higher scores indicate higher degree of stakeholder engagement.

Secondary

MeasureTime frameDescription
Patient Engagement in Research Scale (PEIRS) stakeholder engagement scoreMonth 6The scale consists of 22 items and assesses engagement across seven domains, using a 5-point Likert scale for each item. The 7 domains include: 1) procedural requirements, 2) convenience, 3) contributions, 4) team environment and interaction, 5) support, 6) feel valued, and 7) benefits. The total score is calculated by summing the scores for each item and dividing by the maximum possible score. This result is then multiplied by 100 to get a score out of 100. Higher scores indicate a greater degree of meaningful patient engagement.
Reading grade level of written materialsMonth 6Mean of 5 readability formulas (Flesch Reading Ease, Flesch-Kincaid, Simple Measure of Gobbledygook (SMOG), Gunning Fog, Forcast). Lower score reflects lower reading grade level.
Patient Education Materials Assessment Tool (PEMAT) scoreMonth 6Consists of Understandability (19 items) and Actionability (7 items) subscales. Scoring is as follows: (Total points / possible points yields) x100 = Score %. Higher score reflects greater understandability / actionability.

Countries

United States

Contacts

CONTACTH. Shonna Yin, MD, MS
Hsiang.Yin@nyulangone.org646-501-4284
CONTACTJessica Velazquez-Perez
Jessica.velazquez@nyulangone.org646-501-4288
PRINCIPAL_INVESTIGATORH. Shonna Yin, MD, MS

NYU Langone Health

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 1, 2026