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Pilot-Testing a Family-Based Intervention to Improve Child Outcomes and Increase Family Activity

Pilot-Testing a Family-Based Intervention to Improve Child Outcomes and Increase Family Activity

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01969760
Acronym
HFDC
Enrollment
18
Registered
2013-10-25
Start date
2013-10-31
Completion date
2014-05-31
Last updated
2015-01-28

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

Conditions

Obesity, Overweight, Smoking

Brief summary

The purpose of this study is to examine the feasibility and acceptability of a family-based program to improve physical activity and tobacco outcomes in a small pilot of middle school students and their families.

Detailed description

Low income ethnic minority youth tend to be at greater risk for obesity, physical inactivity, high risk behaviors such as tobacco and substance use and resulting cardiovascular and chronic disease. In this study we modified a tobacco and substance use risk prevention program to develop a tailored intervention (Healthy Families DC) that also included promotion of physical activity (PA) for DC middle-school students referred by school staff as over-weight and at risk for problem behaviors. The program included an initial family assessment, a family feedback session with family PA goal setting and 6 phone/text based booster sessions. A pilot study with 18 families, comprised of at least one caregiver and target child, was conducted to examine feasibility, acceptability, and trends in preliminary outcomes such as PA via self-report and accelerometry, health risk behaviors (e.g., tobacco use), health goal setting, and changes in family functioning (e.g., youth positive behaviors, parenting).

Interventions

BEHAVIORALHealthy Families DC Program

A tailored family-based intervention for health promotion goal setting, substance use prevention, and promotion of physical activity

Sponsors

Cassandra Stanton, PhD
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
12 Years to 16 Years
Healthy volunteers
Yes

Inclusion criteria

* Students aged 12-16 years * Attending regular education classes at three urban DC public middle schools. -Students must currently reside with at least one parent or guardian who wishes to also participate in this study. * Students and at least one guardian must be fluent in English

Exclusion criteria

* Adolescents, who are outside the study age range * Patients/parents unable to speak/read English * Are wards of the state * Not attending regular education classes at the public middle schools -Furthermore, adolescents and guardians not assenting/consenting to be in the study will be excluded.

Design outcomes

Primary

MeasureTime frame
Actigraphy-based changes in physical activity from baseline to 8-weeks post-baseline8-weeks

Secondary

MeasureTime frame
Smoking Susceptibility Scale changes from baseline to 8-weeks post-baseline8 weeks

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026