Skip to content

Is it Helpful to Use Fitbits in a Family Based Weight Loss Program?

Effect of Personal Activity Trackers on Weight Loss in Children Enrolled in a Comprehensive Behavioral Family Lifestyle Intervention (CBFLI) Program

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03215641
Enrollment
200
Registered
2017-07-12
Start date
2015-08-31
Completion date
2019-03-31
Last updated
2018-12-31

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

Conditions

Pediatric Obesity

Keywords

obesity, pediatrics, weight management program, Fitbit, personal activity tracker

Brief summary

This study evaluates the role of personal activity trackers to help improve weight loss or weight maintenance for children and their parents enrolled in a comprehensive weight loss program.

Detailed description

Childhood obesity rates have tripled in the last 30 years, with as many as 50% of children in the US being obese or overweight. High-intensity comprehensive behavioral family lifestyle intervention (CBFLI) programs have been shown to be among the most effective interventions for weight loss in children. However, these programs are time- and resource-intensive with high rates of recidivism. Personal activity trackers (PAT) provide objectively measured physical activity data and are more reliable than self-report. These devices can also have a motivational impact. The investigators intend to study the effects of these devices and their data on behavior change and weight loss for both parents and children enrolled in a CBFLI program. The investigators will objectively measure the level of activity of both members of the parent-child dyad, explore the relationship between parent-child activity levels and its effect on each other, as well as on overall weight loss or weight maintenance.

Interventions

DEVICEFitbit

The Fitbit is a consumer-grade personal activity tracker. It is used to track physical activity. Patients will be given devices at the beginning of the study, and they will continue to use it for 7 weeks. Their data will be collected on a weekly basis, and patients will receive feedback on their level of activity based on the Fitbit data.

Sponsors

Academic Pediatric Association
CollaboratorINDUSTRY
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
CollaboratorNIH
Children's Hospital Los Angeles
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
7 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* All individuals enrolled in BodyWorks who are at least 7 years old meet inclusion criteria for this study. there is no maximum age for participation.

Exclusion criteria

Unable to wear PAT as described in study protocol Unwilling to wear PAT Unwilling to participate in the study

Design outcomes

Primary

MeasureTime frameDescription
BMI-z scoreBaseline to program completion (~8 weeks)change in BMI-z score

Secondary

MeasureTime frameDescription
Impact of fitbit on program attendanceBaseline to program completion (~8 weeks)The investigators will evaluate if families that receive fitbits attend more sessions (out of 7 total sessions) by recording their attendance at each session
impact of fitbit on program completion rateBaseline to program completion (~8 weeks)The investigators will evaluate if families that receive fitbits complete the program at a higher rate (completion is defined as having attended at least 4 out of 7 sessions).

Other

MeasureTime frameDescription
relationship between change in child weight, in Kg, and daily parent steps taken as measured by the FitbitBaseline to program completion (~8 weeksevaluate whether parents who are more active have children who are more likely to lose weight

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 16, 2026