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RecruitingNCT07489079Updated Jun 1, 2026

PlayReadVIP in Family Child Care

An interventional study of PlayReadVIP in Caregiver-Child Interaction and Child Learning, sponsored by NYU Langone Health. Recruiting at 1 site in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-06-01.

Sponsored by NYU Langone Health · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Started May 2026; still recruiting 4 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
240
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

This study uses a mixed-methods, single-group pretest-posttest design to evaluate (1) implementation outcomes (acceptability, adoption, fidelity) and (2) preliminary changes associated with delivery of the adapted PlayReadVIP intervention in Family Care Center (FCC) settings.

02

Conditions studied

  • Caregiver-Child Interaction
  • Child Learning
03

In context

Lead sponsor

NYU Langone Health is the lead sponsor of 1,391 studies on the registry; 254 are open to participants now.

Of its 227 completed or terminated interventional studies of FDA-regulated products, 191 (84%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • 18 years of age or older
  • Family childcare provider or assistant in MARC Network who cares for children who are 0-5 years of age
  • English or Spanish-speaking

Exclusion criteria

Exclusion Criteria:

  • Less than 18 years old
  • Does not speak English or Spanish
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Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
240 participants (estimated)

Study arms

  • Experimental
    FCC Providers + Assistants

    Family child care providers and their assistants.

    Behavioral: PlayReadVIP

Interventions

  • BehavioralPlayReadVIP

    PlayReadVIP (formerly the Video Interaction Project) is an intervention that uses a strengths-based reflective-practice model to coach parents on positive parenting interactions with their children during book reading and play.

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What researchers measure

Primary outcomes

  1. Provider Self-Efficacy

    Provider self-efficacy is measured using the Beliefs About Parent Support for Early Literacy Scale (BPSES). The BPSES consists of items assessing providers' confidence in managing children's behavior and supporting children's development. Items are rated on a 5-point Likert scale ranging from Strongly disagree to Strongly agree. The total score is calculated by summing all five items, and ranges from 5 to 25, with higher scores indicating greater provider self-efficacy.

    Time frame: Pre-Intervention (Baseline), Post-Intervention Session (Day 1 up to Day 30, approximately)

  2. Provider Perceptions of Children's Literacy Practices

    The Provider Perception survey was developed by the NYULH PlayReadVIP research team and includes frequency-based items assessing how often children in the provider's care engage in literacy-related behaviors, social interaction, communication, sustained attention during reading, and challenging behaviors. Each item is rated on a 10-point Likert scale from 0-9. The total score is the sum of responses and ranges from 0-72, with higher scores indicating greater frequency of the specified behaviors.

    Time frame: Pre-Intervention (Baseline), Post-Intervention Session (Day 1 up to Day 30, approximately)

  3. Cognitive Stimulation in the Caregiving Environment

    The StimQ-2 is a standardized, validated caregiver-report measure designed to assess the quality and frequency of cognitive stimulation activities provided to children in early childcare settings. The instrument includes 5-point Likert scale from 0-5 across multiple domains, including shared reading practices, caregiver teaching activities, verbal responsiveness, and availability of developmentally appropriate learning materials. The highest total StimQ Score is 39 and the lowest is 0. Higher scores indicate greater provision of cognitive stimulation within the caregiving environment.

    Time frame: Pre-Intervention (Baseline), Post-Intervention Session (Day 1 up to Day 30, approximately)

Secondary outcomes

  1. Provider Job Stress

    The Child Care Worker Job Stress Inventory (CCW-JSI) is a survey that includes items drawn from three domains: job demands, job resources, and job control. Items are rated on a 5-point frequency scale ranging from 1-5; the total score is calculated as the sum of item responses and ranges from 51 to 255; higher scores indicate greater provider-reported job stress.

    Time frame: Pre-Intervention (Baseline), Post-Intervention Session (Day 1 up to Day 30, approximately)

  2. Caregiver-Child Interaction Quality: Adult Behavior

    Adult Child Interactive Reading Inventory (ACIRI) is an observational measure that assesses adult behaviors across multiple domains, including enhancing children's attention to text, promoting interactive reading and supporting comprehension, and use of literacy-supporting strategies. Each item is rated on a scale from 0-3; the total score is the average of all responses and ranges from 0-3, with higher scores indicating greater caregiver-child interactions.

    Time frame: Pre-Intervention (Baseline), Post-Intervention Session (Day 1 up to Day 30, approximately)

  3. Caregiver-Child Interaction Quality: Child Behavior

    Adult Child Interactive Reading Inventory (ACIRI) is an observational measure that assesses adult behaviors across multiple domains, including enhancing children's attention to text, promoting interactive reading and supporting comprehension, and use of literacy-supporting strategies. Each item is rated on a scale from 0-3; the total score is the average of all responses and ranges from 0-3, with higher scores indicating greater caregiver-child interactions.

    Time frame: Pre-Intervention (Baseline), Post-Intervention Session (Day 1 up to Day 30, approximately)

  4. Classroom Quality

    The Climate of Healthy Interactions for Learning and Development (CHILD) is a standardized observational measure that includes structured observation of classroom practices across nine domains, including transitions, directions and rules, social and emotional learning, adult awareness, adult affect, adult cooperation, adult-child interactions, individualized and developmentally appropriate practices, and child behaviors. The measure consists of 28 easily observable items, scored on a 5-point anchored Likert scale ranging from -2 (very undermining) to +2 (very promoting). The score range is then -2 to +2, with higher score indicating more promoting behavior.

    Time frame: Pre-Intervention (Baseline), Post-Intervention Session (Day 1 up to Day 30, approximately)

  5. Provider-Rated Acceptability, Appropriateness, and Feasibility of Intervention

    After completing all the intervention sessions (up to 3), the provider completes a Provider/Assistant Feedback survey developed by the NYULH PlayReadVIP research team, assessing the acceptability of the intervention. Each item is rated on a 10-point Likert scale from 0-9. The total score ranges from 0-99; higher scores indicate greater overall acceptability of the intervention.

    Time frame: Post-Intervention Session (Day 1 up to Day 30, approximately)

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Study locations

1 of 1 sites recruiting
  • NYU Langone Health
    New York, New York 10016, United States
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 1, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07489079
Lead sponsor
NYU Langone Health
Responsible party
Sponsor
First posted
Mar 23, 2026
Start date
May 27, 2026
Primary completion
Apr 2027 (estimated)
Completion
Apr 2027 (estimated)
Last update
Jun 1, 2026

Study contacts

Denise Mazzuchelli
Contact
Denise.Mazzuchelli@nyulangone.org
917-890-1073
Jade Turbides
Contact
Jade.turbides@nyulangone.org
917-890-1073
Alan Mendelsohn, MD
principal investigator · NYU Langone Health

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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