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Dynamo: a Tailored Lifestyle Promotion Intervention Among Pediatric Patients With Cardiometabolic Risk Factors

Implementing Dynamo: a Tailored Lifestyle Promotion Intervention Among Pediatric Patients With Cardiometabolic Risk Factors

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01736748
Acronym
CIRCUIT
Enrollment
100
Registered
2012-11-29
Start date
2012-08-31
Completion date
2030-12-31
Last updated
2025-05-25

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

Conditions

Obese

Keywords

obesity, physical activity, metabolism, environment, obese children, as defined by a body mass index > 95th percentile, for age and sex

Brief summary

The Dyn@mo lifestyle intervention (CHU Sainte-Justine, Quebec, Canada) targets children and adolescents aged 6 to 17 years old with cardiometabolic risk factors, such as obesity, hypertension, disorders in glucose regulation or dyslipidemia. Its primary goal is to promote physical activity and reduce sedentary time to improve childrens' cardiometabolic profile. To do so, the intervention relies on gathering data on mobility and physical activity using wearable sensors. These data provide a detailed picture of real-life conditions and physical activity levels, improving the health care professional's ability to tailor counseling. The investigators are presently in the implementation phase of this intervention.

Interventions

BEHAVIORALSensor based PA intervention

Children will be equipped with a heart rate monitor, a GPS receiver and an accelerometer for collection of heart rate, mobility and physical activity free-living data during a 7-day period. This will provide a 'spatio-behavioural diagnosis' using a map-based interactive web application. This data will be used to developed a tailored plan to promote physical activity in the child's every day environment.

BEHAVIORALTraditional PA counseling

Children will be encouraged to enhance their physical activity levels using traditional behavioral approaches.

Sponsors

St. Justine's Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
6 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* children ages 6 to 18 years of age with a BMI \> 95th percentile for age and sex

Exclusion criteria

* children with a physical or psychological condition that would impair their ability to participate in physical activity

Design outcomes

Primary

MeasureTime frameDescription
Change in physical activity levelsBaseline and 1 yearPhysical activity will be measured using accelerometry and we will use time spent in moderate to vigorous physical activity as our primary measure of PA

Secondary

MeasureTime frameDescription
Change in blood pressureBaseline and 1 yearBoth systolic and diastolic blood pressure will be measured
Change in glucose homeostasisBaseline and 1 yearBoth fasting blood glucose, and glucose 2hr post load (oral glucose tolerance test) will be measured
Change in lipid statusBaseline and 1 yearLDL, HDL, triglycerides and total cholesterol will be measured at baseline and after 1 year of follow-up
Change in body mass indexBaseline and 1 yearWe will measure height and weight at baseline and at 1 year of follow-up and calculate differences in body mass index over the 1 year period

Countries

Canada

Contacts

Primary ContactMelanie Henderson
514-345-4735
Backup ContactTracie A Barnett
514-345-4931

Outcome results

None listed

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