Water is K'é: Multi-level Intervention to Promote Healthy Beverage Choices Among Navajo Families

March 20, 2025 updated by: Sonya Sunhi Shin, Brigham and Women's Hospital

The goal of this clinical trial is to understand if a cultural intervention for Navajo families will improve healthy beverage habits, health outcomes, and family cohesion. The main questions it aims to answer are:

  • Does Water is K'é results in healthier beverage habits among children aged 2 to 5, compared with children in a control group?
  • Does the intervention improve the health of other family members?
  • How does the intervention affect family well-being?

Participants will take part in a four-month program at the early child education site (such as a Head Start or the Bureau of Indian Affair's Family and Child Education or FACE Program) where the child is enrolled. They will take part in lesson plans, a social media campaign, and a family water access plan. Researchers will compare the participating families with families at wait-list early child educations sites. We will collect information through surveys, health measurements, and qualitative interviews and compare results to learn if Water is K'e improves health behaviors, health outcomes, and family cohesion.

Study Overview

Detailed Description

Water is K'é is a culturally-grounded, family-based intervention designed to promote healthy beverage consumption among Navajo families. Delivered by early child education (ECE) staff, Water is K'é includes three strategies: promoting Diné (Navajo) culture through intergenerational sharing, increasing health literacy about water and sugar-sweetened beverages (SSBs), and increasing drinking water access in both home and ECE settings. Activities consist of a lesson plan for children and caregivers, a tailored access plan to promote confidence in water quality at home and ECE sites; and a social media campaign. Water is K'é is guided by the conceptual framework of the Navajo Wellness Model, addressing four aspects: spiritual; sustenance; family and kinship (K'é); and the environment. The intervention's goal is to promote healthy behaviors and intergenerational sharing of cultural teachings about water, resulting in better health among family members and greater family cohesion overall.

This prospective cluster-randomized trial evaluates the impact of Water is K'é on healthy beverage consumption, health outcomes, and family cohesion. A total of 25 ECE sites will be enrolled in the study, serving in the waitlist group for one year, and then the intervention group the following year based on random assignment. Stepwise roll-out will ensure adequate bandwidth to support intervention sites, while also gathering control data from waitlist sites. Primary caregivers will consent for themselves and the child who is enrolled in the ECE program; other family members will be invited to enroll in the study as well. Each site will enroll approximately 11 families per year, resulting in a total enrollment of 440 families (220 in the intervention group, 220 in the control group) and follow them for 12 months to evaluate the impact on behaviors (beverage consumption patterns) and health outcomes (body mass index, A1c among adults living with diabetes or pre-diabetes) of children and adults. In addition, convergent parallel mixed methods will be used to explore whether Water is K'é results in greater family cohesion through intergenerational cultural continuity. Specific aims are:

  1. Evaluate the impact of Water is K'é on children aged 2 to 5. Hypothesis: participating children will have healthier beverage habits and body mass indices compared with children in the control group.
  2. Evaluate intervention impact on the health of other family members. Hypothesis: participating individuals will have healthier beverage habits and body mass indices compared with the control group.
  3. Evaluate the intervention's impact on family well-being. Hypothesis: participating families will have stronger family cohesion through strengthening of intergenerational cultural continuity compared with families in the control group.

Study Type

Interventional

Enrollment (Estimated)

1160

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Arizona
      • Window Rock, Arizona, United States, 86515
        • Navajo Nation Head Start

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.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • At least one of the following: child enrolled in participating early child education (ECE) program between 2 and 5 years of age; primary caregiver of that child (i.e. identifies as the person who assumes primary caregiver responsibilities of and resides in the same household as the child; or family member aged six or older identified by primary caregiver as an individual in the immediate family who either resides in the same household or visits frequently and day to day interactions with child);
  • Plans to reside in the same household for the next 12 months
  • If enrolled in ECE program, plans to participate in ECE program for the entire school year

Exclusion Criteria:

  • Plans to leave their residence in the next 12 months
  • If enrolled in ECE program, does not plan to participate in ECE program for the entire school year

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Intervention Arm
Water is K'é is a family-based intervention aimed at improving health and wellness of family members and of the family as a whole. The multi-level intervention targets change at environmental, community and family levels through three core activities: a lesson plan, social media campaign and water access plan. ECE staff will receive a brief training on the curriculum and its relation to the Navajo Wellness Model before delivering the lessons and posting messages. Four interactive lesson plans will be delivered by ECE staff. Caregiver and family sessions will be delivered at the Head Start / FACE facility or in the home, depending on staff preference.
Four-month multi-level, family-based intervention that is grounded in Navajo culture and promotes individual knowledge, motivation and skills; social norms; and environmental changes (access to drinking water). At minimum, the enrolled child and primary caregiver will attend monthly sessions, with an open invitation to other family members. Families will also receive social media posts and develop a family access plan by selecting strategies (if needed) to boost their confidence in their water sources at home. ECE sites will also develop a tailored access plan, selecting strategies to increase confidence in water offered at the ECE site, and implement their access plan with study team support.
Other Names:
  • Water is K'e
No Intervention: Control Arm
Participants attending an ECE site randomly assigned to "waitlist" will receive usual programs and services at the site.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Average daily intake of water (fluid ounces) among ECE children
Time Frame: Post intervention (at 4 months) and 8 months after intervention (at 12 months from baseline)
Study arm differences based on Beverage Intake Questionnaire Preschool (BEVQ-PS) measurements in frequency and amount across beverage categories, validated in children under 6
Post intervention (at 4 months) and 8 months after intervention (at 12 months from baseline)
Average daily intake of SSB (fluid ounces) among ECE children
Time Frame: Post intervention (at 4 months) and 8 months after intervention (at 12 months from baseline)
Study arm differences per BEVQ-PS measurements frequency and amount by beverage type, validated in children under 6
Post intervention (at 4 months) and 8 months after intervention (at 12 months from baseline)
Average daily energy intake from SSB (in calories) among ECE children
Time Frame: Post intervention (at 4 months) and 8 months after intervention (at 12 months from baseline)
Study arm differences per BEVQ-PS; measures frequency and amount by beverage type, validated in children under 6
Post intervention (at 4 months) and 8 months after intervention (at 12 months from baseline)
Average daily intake of water (fluid ounces) among family members
Time Frame: Post intervention (at 4 months) and 8 months after intervention (at 12 months from baseline)
Study arm differences per Beverage Intake Questionnaire (BEVQ-15); measures frequency and amount across beverage categories, validated for children 6 and older
Post intervention (at 4 months) and 8 months after intervention (at 12 months from baseline)
Average daily intake of SSB (fluid ounces) among family members
Time Frame: Post intervention (at 4 months) and 8 months after intervention (at 12 months from baseline)
Study arm differences per BEVQ-PS; measures frequency and amount by beverage type
Post intervention (at 4 months) and 8 months after intervention (at 12 months from baseline)
Average daily energy intake from SSB (in calories) among family members
Time Frame: Post intervention (at 4 months) and 8 months after intervention (at 12 months from baseline)
Study arm differences per BEVQ-PS; measures frequency and amount by beverage type, validated in children under 6
Post intervention (at 4 months) and 8 months after intervention (at 12 months from baseline)
Family cohesion score
Time Frame: Post intervention (at 4 months) and 8 months after intervention (at 12 months from baseline)
Study arm differences based on 10-question instrument adapted from Family Adaptability and Cohesion Scale, Short Form (FACES-SF) subscale to measure family cohesion; completed by all family members over 12. For each family, scores from all family members will be averaged to derive a single score per family.
Post intervention (at 4 months) and 8 months after intervention (at 12 months from baseline)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Age-adjusted body mass index z-score among ECE children
Time Frame: Post intervention (at 4 months) and 8 months after intervention (at 12 months from baseline)
Height and weight collected using the National Health and Nutrition Examination Survey (NHANES) protocol
Post intervention (at 4 months) and 8 months after intervention (at 12 months from baseline)
Study arm differences in average World Health Organization-5 (WHO-5) score among family members
Time Frame: Post intervention (at 4 months) and 8 months after intervention (at 12 months from baseline)
WHO-5: 5-item questionnaire to measure well-being; range 0 to 2t with higher score reflecting greater wellbeing
Post intervention (at 4 months) and 8 months after intervention (at 12 months from baseline)
Perceived access to drinking water
Time Frame: Post intervention (at 4 months) and 8 months after intervention (at 12 months from baseline)
Question (Likert score 1-5) on perceived access to reliable drinking water; range 0-5 with higher score reflecting greater access.
Post intervention (at 4 months) and 8 months after intervention (at 12 months from baseline)
Perceived confidence in drinking water
Time Frame: Post intervention (at 4 months) and 8 months after intervention (at 12 months from baseline)
Question (Likert score 1-5) on confidence in drinking water' range 0-5 with higher score reflecting greater confidence.
Post intervention (at 4 months) and 8 months after intervention (at 12 months from baseline)
Knowledge of traditional teachings related to water
Time Frame: Post intervention (at 4 months) and 8 months after intervention (at 12 months from baseline)
Question (Likert score 1-5) on knowledge of Navajo culture related to water; range 0-5 with higher score reflecting greater knowledge.
Post intervention (at 4 months) and 8 months after intervention (at 12 months from baseline)
Influence of traditional teaching on beverage choices
Time Frame: Post intervention (at 4 months) and 8 months after intervention (at 12 months from baseline)
Question (Likert score 1-5) on influence of Navajo culture on what drinks offered to child; range 0-5 with higher score reflecting greater influence.
Post intervention (at 4 months) and 8 months after intervention (at 12 months from baseline)

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Exploratory: Study arm differences in change in glycosylated hemoglobin A1c among individuals living with diabetes or pre-diabetes
Time Frame: Post intervention (at 4 months) and 8 months after intervention (at 12 months from baseline)
Average value of two A1c measures taken at each time point
Post intervention (at 4 months) and 8 months after intervention (at 12 months from baseline)
Exploratory: Study arm differences in average age-adjusted body mass index z-score among family members
Time Frame: Post intervention (at 4 months) and 8 months after intervention (at 12 months from baseline)
Height and weight collected using NHANES protocol
Post intervention (at 4 months) and 8 months after intervention (at 12 months from baseline)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

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 Major Dates

Study Start (Actual)

September 18, 2024

Primary Completion (Estimated)

September 30, 2028

Study Completion (Estimated)

December 31, 2028

Study Registration Dates

First Submitted

August 25, 2023

First Submitted That Met QC Criteria

August 25, 2023

First Posted (Actual)

August 31, 2023

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

March 20, 2025

Last Verified

March 1, 2025

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Per stipulations of the Navajo Research Code, all data belongs to Navajo Nation; researchers would need to direct any request for study data, including IPD, to the Navajo Nation Human Research Review Board

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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