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Smart Heart Trial: Structured Lifestyle Intervention for Overweight and Obese Youth With Operated Heart Defects

The Impact of a Structured Lifestyle Intervention on Body Composition and Exercise Capacity in Overweight Children With Operated Heart Defects

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02980393
Acronym
SHT
Enrollment
40
Registered
2016-12-02
Start date
2012-05-31
Completion date
2016-11-30
Last updated
2016-12-22

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

Conditions

Congenital Heart Disease, Pediatric Obesity

Keywords

congenital heart disease, smart mobile technology, children, adolescents, lifestyle counselling, nutrition, physical activity

Brief summary

This study is to assess whether a lifestyle intervention with diet, exercise and counselling in young patients will have a positive influence on their weight and overall well-being. This study will enrol patients between the ages of 7 to 17 years of age, who have congenital heart disease, and have been identified being overweight or obese. A total of 40 individuals will participate in this study. The study duration will last for 1 year.

Interventions

BEHAVIORALLifestyle intervention

The structured lifestyle intervention involves alternating weekly phone calls with two health coaches: a registered dietitian and a fitness specialist. A total of 50 phone calls (25 nutrition-related and 25 physical activity-related) are delivered over the one-year study. After six months in the program, participants are introduced to supporting program-specific software that they can access online, as an additional way to interact with the program, set goals, and record their progress. Client and family-centred nutrition and physical activity counselling includes an initial and regular behavioural assessment, and subsequent conversations (i.e., phone calls) using motivational interviewing techniques intended to increase knowledge or skills, and improve behaviours.

Sponsors

London Health Sciences Centre
CollaboratorOTHER
Kambiz Norozi
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
7 Years to 17 Years
Healthy volunteers
No

Inclusion criteria

* overweight or obese (BMI\> 85%) patients * between 7-17 years of age * operated or non-operated congenital heart disease * reside in Southwestern Ontario

Exclusion criteria

* inability to comply with research testing or intervention components due to mental and/or physical disabilities, medications or comorbidities affecting weight or metabolic condition * involvement in any concurrent lifestyle intervention program

Design outcomes

Primary

MeasureTime frameDescription
Change in Baseline Body Mass Index (BMI) at 1 yearThis outcome was measured at Baseline, 6 months, 1 year within the 1 year time frameBMI is derived from body mass divided by the square of the body height
Change in Baseline Fat Mass at 1 yearThis outcome was measured at Baseline, 6 months, 1 year within the 1 year time frameDual energy x-ray absorptiometry (DEXA) will measure fat mass.
Change in Baseline Lean Mass at 1 yearThis outcome was measured at Baseline, 6 months, 1 year within the 1 year time frameDual energy x-ray absorptiometry (DEXA) will measure lean mass.
Change in Baseline Percent Fat at 1 yearThis outcome was measured at Baseline, 6 months, 1 year within the 1 year time frameDual energy x-ray absorptiometry (DEXA) will measure percent fat.
Change in Baseline Percent Android Fat at 1 yearThis outcome was measured at Baseline, 6 months, 1 year within the 1 year time frameDual energy x-ray absorptiometry (DEXA) will measure percent android fat.
Change in Baseline Visceral Adipose Tissue at 1 yearThis outcome was measured at Baseline, 6 months, 1 year within the 1 year time frameDual energy x-ray absorptiometry (DEXA) will measure visceral adipose tissue.
Change in Baseline Bone Mineral Content at 1 yearThis outcome was measured at Baseline, 6 months, 1 year within the 1 year time frameDual energy x-ray absorptiometry (DEXA) will measure bone mineral content.
Change in Baseline Maximum Oxygen Consumption at 1 yearThis outcome was measured at Baseline, 6 months, 1 year within the 1 year time frameMaximal exercise graded treadmill test will determine maximal oxygen consumption.

Secondary

MeasureTime frameDescription
Change in Baseline Lipid Profile at 1 yearThis outcome was measured at Baseline, 6 months, 1 year within the 1 year time frameBlood is drawn from patients who have been asked to fast for at least 10 hours.
Change in Baseline Electrolytes at 1 yearThis outcome was measured at Baseline, 6 months, 1 year within the 1 year time frameBlood is drawn from patients who have been asked to fast for at least 10 hours.
Change in Baseline Creatinine at 1 yearThis outcome was measured at Baseline, 6 months, 1 year within the 1 year time frameBlood is drawn from patients who have been asked to fast for at least 10 hours.
Change in Baseline Average Caloric Intake at 1 yearThis outcome was measured at Baseline, 6 months, 1 year within the 1 year time frameAverage caloric intake is estimated from three-day food records.
Change in Baseline Fasting Glucose at 1 yearThis outcome was measured at Baseline, 6 months, 1 year within the 1 year time frameBlood is drawn from patients who have been asked to fast for at least 10 hours.
Change in Baseline Serum Insulin at 1 yearThis outcome was measured at Baseline, 6 months, 1 year within the 1 year time frameBlood is drawn from patients who have been asked to fast for at least 10 hours.
Change in Baseline Adiponectin at 1 yearThis outcome was measured at Baseline, 6 months, 1 year within the 1 year time frameBlood is drawn from patients who have been asked to fast for at least 10 hours.
Change in Baseline Urea at 1 yearThis outcome was measured at Baseline, 6 months, 1 year within the 1 year time frameBlood is drawn from patients who have been asked to fast for at least 10 hours.
Change in Baseline Self-Report Physical Activity Levels at 1 yearThis outcome was measured at Baseline, 6 months, 1 year within the 1 year time framePhysical activity levels will also be measured by the Physical Activity Questionnaire for Older Children
Change in Baseline Physical Activity Levels at 1 yearThis outcome was measured at Baseline, 6 months, 1 year within the 1 year time framePhysical activity levels will be measured from accelerometers
Change in Baseline Quality of Life at 1 yearThis outcome was measured at Baseline, 6 months, 1 year within the 1 year time framePediatric Quality of Life Inventory Generic Core Scales
Change in Baseline Muscle function at 1 yearThis outcome was measured at Baseline, 6 months, 1 year within the 1 year time frameLeonardo Mechanograph® Ground Reaction Force Plate will assess jumping height.
Change in Baseline Electrocardiographic measurement at 1 yearThis outcome was measured at Baseline, 6 months, 1 year within the 1 year time frameElectrocardiogram
Change in Baseline Transthoracic echocardiographic measurement at 1 yearThis outcome was measured at Baseline, 6 months, 1 year within the 1 year time frameEcho-cardiogram will be employed.
Change in Baseline Endothelial vasodilator function at 1 yearThis outcome was measured at Baseline, 6 months, 1 year within the 1 year time framePeripheral arterial tonometry will assess endothelial vasodilator function.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 8, 2026