Actively Recruiting
Implementing Dynamo: a Tailored Lifestyle Promotion Intervention Among Pediatric Patients With Cardiometabolic Risk Factors
Led by St. Justine's Hospital · Updated on 2025-05-25
100
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are studying a tailored lifestyle intervention called Dyn@mo for children and adolescents aged 6 to 17 years who have cardiometabolic risk factors like obesity, high blood pressure, glucose regulation issues, or abnormal cholesterol levels. This intervention aims to increase physical activity and decrease sedentary time to help improve the participants' heart and metabolic health. The study is currently in the phase of implementing this program. Participants are randomly assigned to one of two groups. In the experimental group, children wear sensors including a heart rate monitor, GPS receiver, and accelerometer for seven days to collect detailed data on their heart rate, movement, and physical activity. This information creates a personalized activity plan using an interactive web tool. The control group also wears the sensors but receives traditional physical activity advice without using the sensor data to guide counseling. During the study, researchers measure changes in physical activity levels, blood pressure, glucose control, cholesterol, and body mass index at the start and after one year. Children are monitored using the wearable devices and a web application to support personalized coaching. The study lasts for at least one year, allowing ongoing assessment of how the intervention affects the participants' health and activity habits over time.
CONDITIONS
Brief Title
Dynamo: a Tailored Lifestyle Promotion Intervention Among Pediatric Patients With Cardiometabolic Risk Factors
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Children aged 6 to 18 years
- Body mass index (BMI) above the 95th percentile for age and sex
You will not qualify if you...
- Children with physical conditions that impair their ability to participate in physical activity
- Children with psychological conditions that affect participation in physical activity
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - 7 days
Participants engage in tailored or traditional physical activity promotion interventions using wearable sensors and counseling strategies.
1 week of wearing sensors and receiving intervention
Duration - 1 year
Participants are assessed to evaluate changes in physical activity levels and cardiometabolic risk factors one year after the intervention.
1 follow-up visit at 1 year post-intervention
Trial Site Locations
Total: 1 location
1
CHU Sainte-Justine
Montreal, Quebec, Canada, H3T 1C5
Actively Recruiting
Research Team
M
Melanie Henderson
T
Tracie A Barnett
How is the study designed?
Study Type
INTERVENTIONAL
Masking
QUADRUPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2