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Recruiting NCT01736748

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

No phase Interventional Obese

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Sensor based PA intervention, Traditional PA counseling.
Who it may be relevant to
Registry conditions: Obese. Basic parameters: 6 years — 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Canada
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

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

Overview

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

  • Behavioral Sensor 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.
  • Behavioral Traditional PA counseling
    Children will be encouraged to enhance their physical activity levels using traditional behavioral approaches.

Primary outcome measures

  • Change in physical activity levels [Time frame: Baseline and 1 year]
Secondary outcome measures (4)
  • Change in blood pressure [Time frame: Baseline and 1 year]
  • Change in glucose homeostasis [Time frame: Baseline and 1 year]
  • Change in lipid status [Time frame: Baseline and 1 year]
  • Change in body mass index [Time frame: Baseline and 1 year]

Eligibility criteria

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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Quadruple blind
Primary purpose
Prevention

Study locations

Canada · 1 center
  • CHU Sainte-Justine — Montreal

Identifiers

NCT: NCT01736748 · CIRCUIT 1

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗