- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05741827
YOUhealTH - a Study to Improve Cardiovascular Health in Adolescents and Adults
The goal of this single-center prospective randomized controlled parallel 2-arm intervention study is to test a lifestyle intervention focusing on diet and physical activity in students and at least one legal guardian to improve cardiovascular risk factor profiles.
The primary objective of this study ist to evaluate the efficacy of a health promotion intervention (intervention group) over the course of a year using a participative approach compared to a control group in 14- to 17-year-olds and at least one legal guardian.
Further study objectives are to determine the effect of the health promotion intervention on the change of the score of the individual health metric components, on the absolute health metric score, on the change in intima-media thickness and pulse-wave velocity and cardiovascular health (such as blood pressure, non-HDL-cholesterol, BMI) as well as health literacy with regards to CVDs, especially stroke, in both age-groups.
Furthermore, a biobank will be collected.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
YOUhealTH is a single-center prospective randomized controlled parallel 2-arm intervention study with the aim to test a lifestyle intervention focusing on diet and physical activity in students and at least one legal guardian to improve cardiovascular risk factor profiles. The lifestyle intervention is designed using a participative approach of adolescents who are part of the study team and design the intervention. This intervention is applied to students aged 14- to 17-years and at least one legal guardian for the duration of one year. At the beginning and the end of the intervention, an examination including a blood draw, a structured medical interview, anthropometrics including blood pressure measurement, ultrasonography of the aorta and the carotid artery, pulse-wave velocity and bioelectrical impedance measurement as well as FibroScan (a liver fat and elasticity measurement) is conducted and the effects of the intervention are evaluated compared to the control group receiving no intervention. Students and their legal guardians are randomized to the intervention or control group in a school-wise manner and in a 4:3 ratio.
The primary objective is to determine the effect of the health intervention with regards to the change of the health metric components diet and physical activity of the Life's Essential Eight score of the American Heart Association. Further study objectives are to evaluate the effect of the health promotion intervention on the change of the score of the individual health metric components, on the absolute health metric score, on the change in intima-media thickness and pulse-wave velocity and cardiovascular health (such as blood pressure, non-HDL-cholesterol, BMI) as well as health literacy with regards to CVDs, especially stroke, in both age-groups.
Furthermore, a long-term follow-up by means of record linkage is planned and a biobank will be collected.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Tirol
-
Innsbruck, Tirol, Austria, 6020
- Department for Neurology, Medical University of Innsbruck
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Adolescents at the age of 14 to 17 years and at least one legal guardian willing to participate
- Signed informed consent of subjects and legal guardian
Exclusion Criteria:
- Persons, who are suspended upon a court order or upon other legal processes or are accommodated according to the Hospitalization Act, or for whom a custodian is appointed (or appointment is initiated).
- Persons with impaired power of judgment
- Persons who are currently engaged in military or community service
- Pregnancy of study participants
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Interventional group
Lifestyle intervention with focus on increased physical activity and healthy diet.
|
Lifestyle intervention focusing on diet and physical activity
|
|
No Intervention: Control group
No lifestyle intervention.
No change in physical activity or diet.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Efficacy of health promotion intervention
Time Frame: Baseline visit until follow-up visit (at 12 +/- 2 months)
|
The efficacy of the health promotion intervention to improve cardiovascular health in 14- to 17 year-olds and at least one legal guardian measured by means of change of the "2022 cardiovascular health metrics score (0-100 points)" for the components of diet and physical activity from baseline to follow-up of the intervention group using a participative approach compared to a control-group.
|
Baseline visit until follow-up visit (at 12 +/- 2 months)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Health promotion intervention
Time Frame: Baseline visit until follow-up visit (at 12 +/- 2 months)
|
The effect of the health promotion intervention on both the change and the absolute values of the "2022 cardiovascular health metrics score (0-100 points)" and its components in the whole study group and in adolescents and adults separately.
|
Baseline visit until follow-up visit (at 12 +/- 2 months)
|
|
Health literacy
Time Frame: Baseline visit until follow-up visit (at 12 +/- 2 months)
|
The effect of the health intervention on health literacy (measured by means of a CVD (HELMA; score) and stroke knowledge questionnaire (%)).
|
Baseline visit until follow-up visit (at 12 +/- 2 months)
|
|
Pulse-wave velocity change
Time Frame: Baseline visit until follow-up visit (at 12 +/- 2 months)
|
The effect of the health intervention on pulse-wave velocity (m/s)
|
Baseline visit until follow-up visit (at 12 +/- 2 months)
|
|
Intima-media thickness change
Time Frame: Baseline visit until follow-up visit (at 12 +/- 2 months)
|
The effect of the health intervention on intima-media thickness (µm).
|
Baseline visit until follow-up visit (at 12 +/- 2 months)
|
|
Liver fat content change
Time Frame: Baseline visit until follow-up visit (at 12 +/- 2 months)
|
The effect of the health intervention on liver fat content (dB/m).
|
Baseline visit until follow-up visit (at 12 +/- 2 months)
|
|
Blood pressue change
Time Frame: Baseline visit until follow-up visit (at 12 +/- 2 months)
|
The effect of the health intervention on blood pressure (mmHg).
|
Baseline visit until follow-up visit (at 12 +/- 2 months)
|
|
Body-/fat composition change
Time Frame: Baseline visit until follow-up visit (at 12+/- 2 months)
|
The effect of the health intervention on body-/fat composition (%)
|
Baseline visit until follow-up visit (at 12+/- 2 months)
|
|
Visceral fat thickness change
Time Frame: Baseline visit until follow-up visit (at 12+/- 2 months)
|
The effect of the health intervention on abdominal visceral fat thickness (mm).
|
Baseline visit until follow-up visit (at 12+/- 2 months)
|
|
Physical activity change
Time Frame: Baseline visit until follow-up visit (at 12 +/- 2 months)
|
The effect of the health intervention on the average minutes of moderate to vigorous physical activity per day (min/day).
|
Baseline visit until follow-up visit (at 12 +/- 2 months)
|
|
Risk profile - e.g. blood lipids
Time Frame: Baseline visit until follow-up visit (at 12 +/- 2 months)
|
Risk profiles (e.g.
blood lipids such as LDL-C (mg/dl)) of adolescents will be compared to their legal guardian(s).
|
Baseline visit until follow-up visit (at 12 +/- 2 months)
|
|
Risk profile - e.g. Blood sugar
Time Frame: Baseline visit until follow-up visit (at 12+/- 2 months)
|
Risk profiles (e.g.
blood sugar (HbA1c (%)) of adolescents will be compared to their legal guardian(s).
|
Baseline visit until follow-up visit (at 12+/- 2 months)
|
|
Risk profile - Healthy diet
Time Frame: Baseline visit until follow-up visit (at 12+/- 2 months)
|
Risk profiles (healty diet (MEPA score;%)) of adolescents will be compared to their legal guardian(s).
|
Baseline visit until follow-up visit (at 12+/- 2 months)
|
|
Risk profile - Smoking
Time Frame: Baseline visit until follow-up visit (at 12+/- 2 months)
|
Risk profiles (smoking (questionnaire, score) of adolescents will be compared to their legal guardian(s).
|
Baseline visit until follow-up visit (at 12+/- 2 months)
|
|
Cardiovascular risk factor description - hypertension
Time Frame: Baseline visit until follow-up visit (at 12 +/- 2 months)
|
The prevalence of traditional cardiovascular risk factors such as hypertension (mmHg) in the Tyrolean youth and their legal guardians will be described.
|
Baseline visit until follow-up visit (at 12 +/- 2 months)
|
|
Cardiovascular risk factor description - obesity
Time Frame: Baseline visit until follow-up visit (at 12+/- 2 months)
|
The prevalence of traditional cardiovascular risk factors such as obesity (e.g.BMI (kg/m^2)) in the Tyrolean youth and their legal guardians will be described.
|
Baseline visit until follow-up visit (at 12+/- 2 months)
|
|
Cardiovascular risk factor description - dislipidemia
Time Frame: Baseline visit until follow-up visit (at 12+/- 2 months)
|
The prevalence of traditional cardiovascular risk factors such as dyslipidemia (e.g.
LDL-C (mg/dl)) in the Tyrolean youth and their legal guardians will be described.
|
Baseline visit until follow-up visit (at 12+/- 2 months)
|
|
Cardiovascular risk factor description - diabetes
Time Frame: Baseline visit until follow-up visit (at 12+/- 2 months)
|
The prevalence of traditional cardiovascular risk factors such as diabetes (HbA1c (%)) in the Tyrolean youth and their legal guardians will be described.
|
Baseline visit until follow-up visit (at 12+/- 2 months)
|
|
Lifestyle factor description - unhealthy diet
Time Frame: Baseline visit until follow-up visit (at 12+/- 2 months)
|
The prevalence of lifestyle factors such as unhealthy diet (MEPA-score; %) in the Tyrolean youth and their legal guardians will be described.
|
Baseline visit until follow-up visit (at 12+/- 2 months)
|
|
Lifestyle factor description - sedentary lifestyle
Time Frame: Baseline visit until follow-up visit (at 12+/- 2 months)
|
The prevalence of lifestyle factors such as sedentary lifestyle (Physical activity component of of Life's Essential 8 assessment; %) in the Tyrolean youth and their legal guardians will be described.
|
Baseline visit until follow-up visit (at 12+/- 2 months)
|
|
Lifestyle factor description - smoking
Time Frame: Baseline visit until follow-up visit (at 12+/- 2 months)
|
The prevalence of lifestyle factors such as smoking (YES/NO, cigarettes per day) in the Tyrolean youth and their legal guardians will be described.
|
Baseline visit until follow-up visit (at 12+/- 2 months)
|
|
High-risk population exploration
Time Frame: Baseline visit until follow-up visit (at 12+/- 2 months)
|
High-risk populations (Life's essential 8 score; %) based on school type, age, sex and region of residence will be explored.
|
Baseline visit until follow-up visit (at 12+/- 2 months)
|
|
Time trends
Time Frame: Baseline visit until follow-up visit (at 12+/- 2 months)
|
Time trends in risk-profiles will be evaluated by comparison to the data from the "Early vascular Ageing" and the "Early Vascular Ageing in YOUth" study.
|
Baseline visit until follow-up visit (at 12+/- 2 months)
|
|
Long-term Intervention - CVD events
Time Frame: Every 2-5 years, on average for the duration of 50 years
|
Evaluation of predictors for later cardio- and cerebrovascular disease (events or deaths) in adolescents and their legal guardian by record linkage to electronic health record.
|
Every 2-5 years, on average for the duration of 50 years
|
|
Long-term Intervention - any deaths
Time Frame: Every 2-5 years, on average for the duration of 50 years
|
Evaluation of predictors for later mortality in adolescents and their legal guardian by record linkage to death registry.
|
Every 2-5 years, on average for the duration of 50 years
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Michael Knoflach, Assoc.-Prof., Medical University of Innsbruck
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- nC_FNA-0029_004
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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