Skip to content

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

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

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05612971
Enrollment
480
Registered
2022-11-14
Start date
2023-10-23
Completion date
2026-09-01
Last updated
2026-03-30

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

Conditions

Pediatric Obesity, Weight Loss

Brief summary

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.

Detailed 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.

Interventions

BEHAVIORALiAmHealthy Parents First

iAmHealthy Parents first is a 3-month adult obesity treatment program targeting the unique needs of adults with school-age children. Following the iAmHealthy Parents First program, these dyads will take part in a 6-month family-based healthy lifestyles program.

BEHAVIORALiAmHealthy

The iAmHealthy group will receive newsletters for three months. Following this period, these dyads will take part in a 6-month family-based healthy lifestyles program.

Sponsors

University of Kansas Medical Center
Lead SponsorOTHER
National Institutes of Health (NIH)
CollaboratorNIH
National Institute of Nursing Research (NINR)
CollaboratorNIH

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
6 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Percent weight change in parents and BMIz (BMI z-score) in childrenBaseline, 3 months, 9 monthsParents and children will measure body weight on a study-provided digital scale following instructions provided by study team.

Secondary

MeasureTime frameDescription
Mediator: AttendanceBaseline, 3 months, 9 monthsGroup and individual session attendance (percent of sessions) will be tracked on REDCap, a secure, web-based application designed exclusively to support data capture for research studies.
Mediator: Reciprocal modelingBaseline, 3 months, 9 monthsReciprocal influence (parent response as mediator for child; child response as mediator for parent) will be operationalized as adult or child weight loss.
Moderator: Family functioningBaseline, 3 months, 9 monthsFamily functioning will be measured using the Family Assessment Device (FAD). This is the gold-standard measure of structural, organizational, and transactional characteristics of families including general family functioning (core scale of interest) and 6 additional subscales: affective involvement, affective responsiveness, behavioral control, communication, problem solving, and roles. This questionnaire will be completed by adults. The FAD is scored by adding responses of each scale (1 - 4) and dividing by the number of items in each scale (between 6 - 12). The higher the overall score, the worse the level of family function.
Moderators: Genetic casual attributionsBaseline, 3 months, 9 monthsGenetic casual attributions will be measured using a a 2-item Likert scale that assesses perceived genetic role for weight status and potential for weight loss. This will be completed by adults. Those who endorse completely or mostly for the role of genes in weight loss will be characterized as having "high genetic attribution" for weight status.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORAnn M Davis, PhD, MPH

University of Kansas Medical Center

PRINCIPAL_INVESTIGATORChristie Befort, PhD

University of Kansas Medical Center

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 31, 2026