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iAmHealthy Parents First: A Televideo Parent and Child Obesity Program for Rural Families

University of Kansas logo

University of Kansas

Status

Active, not recruiting

Conditions

Weight Loss
Pediatric Obesity

Treatments

Behavioral: iAmHealthy Parents First
Behavioral: iAmHealthy

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT05612971
STUDY00147611
R01NR019810 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The purpose of this study is to assess whether providing a parent-only group program before providing a parent and child group program works better than the parent and child group program alone.

Full description

The goal of this project is to determine if an adult intervention followed by a family-based program (iAmHealthy Parents First) will result in a larger percentage of weight loss in parents and children compared to solely a family-based program (iAmHealthy). Furthermore, the investigators aim to discover if administering iAmHealthy Parents First will improve dietary intake, physical activity, and weight-related quality of life among parents and children when compared to iAmHealthy. Parent/child dyads will be recruited from rural elementary schools, medical clinics, and organizations across Kansas and neighboring states.

Enrollment

480 estimated patients

Sex

All

Ages

6+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Family lives in a rural area (city and/or county population <20,000) or as defined by RUCA codes, Urban Influence Codes, amount of agricultural income, or individual commuting patterns
  • Child BMI%ile ≥ 85th and parent BMI 25-50 kg/m2
  • Child in 1st-5th grade or 6-11 years of age
  • Child and parent speak English
  • Family is available at times intervention is offered

Exclusion criteria

  • For parents: new MI, stroke or cancer diagnosis in past 6 months, recent bariatrics surgery (within 2 years) or planned within 1 year, pregnancy in last 6 months or planned within 1 year

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

480 participants in 2 patient groups

iAmHealthy Parents First
Experimental group
Description:
iAmHealthy Parents First families will take part in a group program with other adults over Zoom. Children will not be involved during this time. Adults will participate in these group sessions weekly for three months. Each meeting will last approximately an hour. Fifteen dyads from each cohort will be randomized to the iAmHealthy Parents First group. After 3 months, both iAmHealthy Parents First and iAmHealthy families will take part in an educational group program with parents and their children. These meetings will be focused on living healthy lifestyles and engaging in healthy habits as a family and will occur three weeks out of four for four months. There will be three additional family-based group sessions spread over the final two months of the program. iAmHealthy Parents First adults will continue to meet monthly during the family-based program (on weeks when the family-based group does not meet) to continue the adult program.
Treatment:
Behavioral: iAmHealthy Parents First
iAmHealthy
Active Comparator group
Description:
iAmHealthy families will receive an informational newsletter once a month for three months. This group will be given the flexibility to start their weight loss journey using self-guided methods. No formal group sessions will be provided for three months. Fifteen dyads from each cohort will be randomized to the iAmHealthy group. After 3 months, both iAmHealthy Parents First and iAmHealthy families will take part in an educational group program with parents and their children. These meetings will be focused on living healthy lifestyles and engaging in healthy habits as a family and will occur three weeks out of four for four months. There will be three additional family-based group sessions spread over the final two months of the program.
Treatment:
Behavioral: iAmHealthy

Trial contacts and locations

1

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Central trial contact

Megan Olalde, MS

Data sourced from clinicaltrials.gov

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