NCT07197216

Brief Summary

The primary aim of this clinical trial is to determine whether the Tap Trust intervention increases water intake among preschool-aged children and their parents/caregivers by improving families' experiences with their home tap water.

Trial Health

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
100

participants targeted

Target at P50-P75 for not_applicable

Timeline
16mo left

Started Nov 2025

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
enrolling by invitation

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress27%
Nov 2025Sep 2027

First Submitted

Initial submission to the registry

September 19, 2025

Completed
10 days until next milestone

First Posted

Study publicly available on registry

September 29, 2025

Completed
1 month until next milestone

Study Start

First participant enrolled

November 7, 2025

Completed
1.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2027

Expected
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2027

Last Updated

November 12, 2025

Status Verified

November 1, 2025

Enrollment Period

1.6 years

First QC Date

September 19, 2025

Last Update Submit

November 10, 2025

Conditions

Keywords

Drinking water qualityChild beverage intakePreschoolers

Outcome Measures

Primary Outcomes (1)

  • Change in child total plain water intake (oz/day)

    Child total plain water intake assessed via validated beverage frequency questionnaires

    Baseline and 6 months post-intervention

Secondary Outcomes (10)

  • Change in child unfiltered tap water intake (oz/day)

    Baseline and 6 months post-intervention

  • Change in child filtered tap water intake (oz/day)

    Baseline and 6 months post-intervention

  • Change in child bottled water intake (oz/day)

    Baseline and 6 months post-intervention

  • Change in child sugar-sweetened beverages (SSB) intake (oz/day)

    Baseline and 6 months post-intervention

  • Change in parent/caregiver total plain water intake (oz/day)

    Baseline and 6 months post-intervention

  • +5 more secondary outcomes

Study Arms (2)

Intervention Group

EXPERIMENTAL

Participants will test their home tap water using kits mailed to their homes, with phone or Zoom assistance from the research team. Families with water quality concerns will receive remediation tailored to the issue (e.g., flushing guidance, filtration device and installation guidance). Participants will also receive reusable water bottles, educational handouts and videos, and phone or Zoom sessions with the research team that include motivational interviewing to set healthy beverage goals.

Behavioral: Tap Trust

Control Group

NO INTERVENTION

Participants will not receive water testing kits, filtration devices, or educational resources during the study. After the study concludes, participants will have access to the intervention materials.

Interventions

Tap TrustBEHAVIORAL

Home-based intervention includes tap water testing kits (instructions provided with videos or phone/Zoom), filtration devices if water quality concerns are identified, reusable water bottles and educational materials (handouts and videos), and phone/Zoom sessions with the research team using motivational interviewing.

Intervention Group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Parents/caregivers of pre-school aged children from the Healthy Drinks, Healthy Futures study childcare centers that did not receive the program.
  • Parents/caregivers must speak English or Spanish.
  • Parents/caregivers of preschool-age children who don't have health conditions that preclude intake of water.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Stanford University

Stanford, California, 94305-5119, United States

Location

Study Officials

  • Anisha I Patel, MD, MSPH

    Stanford University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor of Pediatrics

Study Record Dates

First Submitted

September 19, 2025

First Posted

September 29, 2025

Study Start

November 7, 2025

Primary Completion (Estimated)

July 1, 2027

Study Completion (Estimated)

September 1, 2027

Last Updated

November 12, 2025

Record last verified: 2025-11

Locations