Actively Recruiting

Phase Not Applicable
Age: 6Years - 18Years
All Genders
ID01736748

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

Age: 6Years - 18Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Children aged 6 to 18 years
  • Body mass index (BMI) above the 95th percentile for age and sex
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Outpatient Treatment

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

Follow-up

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

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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

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