- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05974826
Healthy Communities: a Healthy City Preventive Program on Cardiovascular Health and Well-being (HC) (HC)
Impact of a Healthy City Preventive Program on Cardiovascular Health and Well-being: a Quasi-Experimental Controlled Longitudinal Community-Based Study (Healthy Communities 2030)
Healthy Communities is a multidisciplinary health-promotion initiative. The objective of the present study is to determine whether such an intervention will be efficacious to improve cardiovascular health compared to the current approach.
A quasi-experimental controlled longitudinal community-based intervention study will be carried out comprising approximately 2000 individuals from the age of 12 years from the cities of Cardona (intervention city) and Sallent (control city), in Spain. The core of the intervention will be based on the previous health promotion programs developed and evaluated by the Science, Health and Education (SHE) Foundation: the SI! Program (Salud Integral -Comprehensive Health) for children, and the Fifty-Fifty Program for adults. Coupled to infrastructure development, we will promote the understanding of the benefits of active living to increase awareness on the relevance of healthy lifestyle to improve health and wellbeing in three consecutive phases (Phase 1- full supervised program; Phase 2- transition period, and Phase 3- self-community driven program), which will provide full empowerment to the community.
The primary outcome will be measured with the validated composite Fuster-BEWAT (Blood pressure, Exercise/physical activity, body Weight/BMI, Alimentation/diet, and Tobbaco/smoking) score consisting of a 0-15 scale for behaviors/health risk factors. Assessments will be performed at baseline, at 2.5 and 5 years. Follow-up assessments will be conducted to determine the between group differences (intervention vs. control) in the change of the Fuster-BEWAT score at phase 2 and phase 3.
Study Overview
Status
Detailed Description
Healthy Communities is a multidisciplinary health-promotion initiative aiming to improve the health and wellbeing of individuals using an innovative combination of programs and urban design to build up a "culture of health". The main aim is to turn cities and towns into places where individuals, families, and communities can increase their health and welfare potential, and where working toward cardiovascular health and wellbeing is everyone's business.
The objective of the present study is to determine whether such an intervention will be efficacious compared to the current approach.
The hypothesize is that a healthy city will impact positively to their inhabitants by improving cardiovascular health and physical activity indices, mental health, and wellbeing. For such a purpose, a controlled longitudinal community-based intervention study will be carried out on 2000 participants (1000 in the intervention and 1000 in the control towns) 12 years or older over a period of 5 years.
The core of the intervention will be based on the previous health promotion programs developed and evaluated by the Science, Health and Education (SHE) Foundation: the SI! Program for children, and the "Fifty-Fifty" Program for adults. The effect of these interventions was proven through randomized trials and the results were published in high-impact journals (Journal of the American College of Cardiology, American Heart Journal, American Journal of Medicine, etc.).
- The "SI!" Program is a school-based intervention aimed at promoting cardiovascular Health among children aged 3 to 16 years using their proximal environment (school, teachers, and families). The intervention is designed to instill and develop healthy behaviors in relation to diet, physical activity, and emotions, all connected to cardiovascular health.
- The "Fifty-Fifty" Program is a peer-group based intervention about topics related to physical activity, nutrition, and psychological aspects of lifestyle change, which is adapted to 3 different aged groups: "Fifty-Action" for young adults aged 17 to 24 years, "Fifty-Fifty" for people aged 25 to 50 years and "Fifty-Plus" for people over 51 years of age.
Coupled to infrastructure development, we will promote the understanding of the benefits of active living to increase awareness on the relevance of healthy lifestyle to improve health and wellbeing in three consecutive phases, which will provide full empowerment to the community.
During the first phase, a full educational and behavioral change program with specific actions and activities to engage and promote health and wellbeing in the community will be implemented; while the second phase will be a transition period where the Cardona inhabitants will progressively acquire a key role in such implementation under moderate supervision. Finally, during phase 3, we expect that the community will become totally empowered to drive their own health and wellbeing promotion program under minimal supervision. A non-intervention town -Sallent, in the same area- will serve as control group.
The primary outcome will be measured with the validated composite Fuster-BEWAT score consisting of a 0-15 scale for behaviors/health risk factors related to Blood pressure, Exercise, Weight, Alimentation (diet), and Tobacco (smoking). Assessments will be performed at baseline, at 2.5 and 5 years. Follow-up assessments will be used to calculate the between group differences (intervention vs. control) for the change in the Fuster-BEWAT score at midpoint of phase 2 (after the full supervised program and during the transition period), and at phase 3 (self-community driven program). Each study visit will include clinical interview, physical examination (height, weight, waist circumference, blood pressure and heart rate), point-of-care testing of lipid and glucose profile, lifestyle and behavior questionnaires, assessment of physical activity, evaluation of muscle strength and muscle quality, and assessment of psychosocial well-being. Trained health personnel will conduct all interviews and measurements.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Madrid, Spain, 28001
- Foundation for Science, Health and Education
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Age greater than or equal to 12 years
- Registered in the local census of the selected towns (Cardona or Sallent)
Exclusion Criteria:
- Age less than 12 years
- Residency out of the selected towns (Cardona or Sallent)
- Unable/unwilling to provide informed consent
- Severe diseases
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Community Intervention (town: Cardona)
The interventions aim to encourage a healthy lifestyle, including diet education, physical activity, and wellbeing. The SI! Program for Secondary Schools: a four-year specially designed educational program for adolescents is applied. The Fifty-Fifty Program implies two stages: 1) Training period; 2) a Peer-group intervention, designed to make the subjects participate actively in their healthcare |
The SI! Program is implemented from 1st to 4th grade of Secondary Schools.
A total of 12 hours of classroom intervention per academic year, organized through three educational units, and with active and participative methodologies, and complementary intervention in the family setting, at school and on teachers.
|
|
No Intervention: Community Control (town: Sallent)
The participants on the control group only receive general health recommendation at the end of each assessment.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Changes of the Fuster-BEWAT
Time Frame: baseline, 3 and 5 years
|
The primary outcome will be the change from baseline in composite Fuster-BEWAT score consisting of a 0-15 scale for the following behaviors/health risk factors (higher scores correspond to healthier lifestyles): Blood pressure (systolic and diastolic blood pressure), Exercise (minutes of vigorous and moderate physical activity), Weight (body mass index calculated as body weight divided by height squared (kg/m2), Alimentation (diet) (fruits and vegetables consumption), and Tobacco (smoking) (smoking status and number of cigarettes) (0-3 points for each domain).
Higher scores correspond to healthier lifestyle behaviors.
The primary outcome is whether individuals belonging to a lifestyle intervention program (intervention group) demonstrate an improvement of health related behaviors and biological parameters compared to the self-management approach (control group).
|
baseline, 3 and 5 years
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Changes at follow-up visits of individual domains of the Fuster-BEWAT score
Time Frame: baseline, 3 and 5 years
|
Mean score and change at follow-up visits for each of the individual domains assimilated in the composite Fuster-BEWAT score (0-3 points for each domain, higher scores correspond to healthier lifestyles): Blood pressure (systolic and diastolic blood pressure), Exercise (minutes of vigorous and moderate physical activity), Weight (body mass index calculated as body weight divided by height squared (kg/m2)), Alimentation (diet) (fruits and vegetables consumption), and Tobacco (smoking) (smoking status and number of cigarettes).
Higher scores correspond to higher compliance to lifestyle guidelines.
|
baseline, 3 and 5 years
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Changes at follow-up visits of blood pressure
Time Frame: baseline, 3 and 5 years
|
Mean and change in blood pressure (systolic and diastolic) (mmHg) as assessed with a fully automated blood pressure monitor (OMRON M6 monitor).
|
baseline, 3 and 5 years
|
|
Changes at follow-up visits of physical activity
Time Frame: baseline, 3 and 5 years
|
Mean and change in physical activity as evaluated by self-reported the short version of the Minnesota Leisure Time Physical Activity Questionnaire (REGICOR).
The questionnaire calculates energy expenditure from total physical activity, and from light, moderate and vigorous physical activity (minutes per week).
|
baseline, 3 and 5 years
|
|
Changes at follow-up visits of body mass index
Time Frame: baseline, 3 and 5 years
|
Mean and change in body mass index (kg/m2).
Body height as measured using a stadiometer (Seca 213).
Body weight as measured using the OMRON BF511 electronic scale.
|
baseline, 3 and 5 years
|
|
Changes at follow-up visits of Mediterranean diet adherence
Time Frame: baseline, 3 and 5 years
|
Change in the adherence to a Mediterranean diet as evaluated by a self-reported the Short Diet Quality Screener (SDQS) questionnaire.
Score range=0-36 (higher scores correspond to highest healthy diet).
|
baseline, 3 and 5 years
|
|
Changes at follow-up visits of smoking status
Time Frame: baseline, 3 and 5 years
|
Mean and change in smoking status as evaluated by self-reported the average number of cigarettes products consumed daily.
|
baseline, 3 and 5 years
|
|
Changes at follow-up visits of blood glucose and lipid profile
Time Frame: baseline, 3 and 5 years
|
Mean total, LDL- and HDL-cholesterol (mg/dL), and blood glucose (mg/dL) and change at follow-up visits as evaluated by point-of-care testing.
Blood glucose and lipid profile were measured using a CardioCheck Plus device and PTS-Panels test strips in capillary blood sampled with a lancet in fasting status.
|
baseline, 3 and 5 years
|
|
Changes at follow-up visits of body fat composition
Time Frame: baseline, 3 and 5 years
|
Mean and change in body fat mass and body lean mass as measured by bioelectrical impedance.
|
baseline, 3 and 5 years
|
|
Changes at follow-up visits of muscle strength
Time Frame: baseline, 3 and 5 years
|
Mean and change in muscle strength evaluated by the hand-grip test (kg)
|
baseline, 3 and 5 years
|
|
Changes at follow-up visits of psychosocial wellbeing
Time Frame: baseline, 3 and 5 years
|
Change in psychosocial wellbeing as evaluated by self-reported questionnaire about perceived happiness (Pemberton Happiness Index), Score range=0-10 (higher scores correspond to highest psychosocial wellbeing).
|
baseline, 3 and 5 years
|
|
Changes at follow-up visits of perceived stress
Time Frame: baseline, 3 and 5 years
|
Change in perceived stress as evaluated by self-reported questionnaire Perceived Stress Scale (14-items PSS).
Score range=0-56 (higher scores correspond to highest perceived stress).
|
baseline, 3 and 5 years
|
|
Changes at follow-up visits of social support
Time Frame: baseline, 3 and 5 years
|
Change in social support as evaluated by self-reported questionnaire Spanish-translated ENRICHD Social Support Instrument.
Score range=0-21 (higher scores correspond to highest social support).
|
baseline, 3 and 5 years
|
|
Changes at follow-up visits of resilience
Time Frame: baseline, 3 and 5 years
|
Change in resilience as evaluated by self-reported questionnaire Spanish-adaptation of Brief Resilience Coping Scale.
Score range=4-20 (higher scores correspond to highest resilience).
|
baseline, 3 and 5 years
|
|
Changes at follow-up visits of self-esteem
Time Frame: baseline, 3 and 5 years
|
Change in self-esteem as evaluated by self-reported questionnaire Child Health and Illness Profile-Adolescent Edition (CHIP-AE).
Score range=1-20 (higher scores correspond to highest self-esteem).
|
baseline, 3 and 5 years
|
|
Changes at follow-up visits of mood
Time Frame: baseline, 3 and 5 years
|
Change in mood as evaluated by self-reported a Spanish questionnaire design by Vazquez-Fernandez ME et al 2013.
Score range=0-6 (scoring ≥3 means mood is negative).
|
baseline, 3 and 5 years
|
|
Changes in the proportion of participants with any positive modifications in behavior
Time Frame: baseline, 3 and 5 years
|
Changes in the proportion of participants with any positive modifications in behavior
|
baseline, 3 and 5 years
|
Collaborators and Investigators
Investigators
- Principal Investigator: Valentin Fuster, Mount Sinai Hospital
Publications and helpful links
General Publications
- Gomez-Pardo E, Fernandez-Alvira JM, Vilanova M, Haro D, Martinez R, Carvajal I, Carral V, Rodriguez C, de Miguel M, Bodega P, Santos-Beneit G, Penalvo JL, Marina I, Perez-Farinos N, Dal Re M, Villar C, Robledo T, Vedanthan R, Bansilal S, Fuster V. A Comprehensive Lifestyle Peer Group-Based Intervention on Cardiovascular Risk Factors: The Randomized Controlled Fifty-Fifty Program. J Am Coll Cardiol. 2016 Feb 9;67(5):476-85. doi: 10.1016/j.jacc.2015.10.033. Epub 2015 Nov 9. Erratum In: J Am Coll Cardiol. 2016 Mar 22;67(11):1385.
- Fernandez-Alvira JM, Fuster V, Pocock S, Sanz J, Fernandez-Friera L, Laclaustra M, Fernandez-Jimenez R, Mendiguren J, Fernandez-Ortiz A, Ibanez B, Bueno H. Predicting Subclinical Atherosclerosis in Low-Risk Individuals: Ideal Cardiovascular Health Score and Fuster-BEWAT Score. J Am Coll Cardiol. 2017 Nov 14;70(20):2463-2473. doi: 10.1016/j.jacc.2017.09.032.
- Fernandez-Jimenez R, Santos-Beneit G, Tresserra-Rimbau A, Bodega P, de Miguel M, de Cos-Gandoy A, Rodriguez C, Carral V, Orrit X, Haro D, Carvajal I, Ibanez B, Storniolo C, Domenech M, Estruch R, Fernandez-Alvira JM, Lamuela-Raventos RM, Fuster V. Rationale and design of the school-based SI! Program to face obesity and promote health among Spanish adolescents: A cluster-randomized controlled trial. Am Heart J. 2019 Sep;215:27-40. doi: 10.1016/j.ahj.2019.03.014. Epub 2019 Apr 10.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
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
- SHE-003-HC
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
the de-identified data underlying results in a publication will be shared on reasonable request to the principal investigator.
Email: estudio@fundacionshe.org
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.
Clinical Trials on Health Behavior
-
Holbaek SygehusCompletedHealth Behavior | Health Knowledge, Attitudes, Practice | Health-Related Behavior | Health LiteracyDenmark
-
Penn State UniversityCompletedBehavior, HealthUnited States
-
Henry Ford Health SystemUniversity of Kansas; University of Maryland, College ParkActive, not recruiting
-
Istinye UniversityRecruitingHealth-Related BehaviorTurkey (Türkiye)
-
University of Texas Rio Grande ValleyHealth and Human Services Commission (HHSC); Pharr-San Juan-Alamo Independent... and other collaboratorsCompletedHealth-Related BehaviorUnited States
-
University of PrimorskaUniversity of Ljubljana, Faculty of Social Sciences; Ministry of Defence, SloveniaActive, not recruitingHealth-Related BehaviorSlovenia
-
Boston Children's HospitalAllan & Gill Gray FoundationCompletedSleep | Health-Related BehaviorUnited States
-
University of LisbonRecruitingOral Health Behavior Change | Oral Health Care | Oral Health Self-efficacyPortugal
-
Boston Children's HospitalRecruitingSleep | Health-Related BehaviorUnited States
-
Universiti Teknologi MaraUniversiti Putra Malaysia; Ministry of Health, Malaysia; Institute for Health... and other collaboratorsRecruitingHealth Attitude | Health Behavior | Knowledge, Attitudes, Practice | Health Knowledge, Attitudes, Practice | Health-Related Behavior | Behavior, Health | Attitude to Health | Preparedness | OutbreaksMalaysia
Clinical Trials on the SI! Program for Secondary Schools (NCT03504059)
-
Public Health Agency of BarcelonaCompleted
-
Istituto Nazionale di Ricovero e Cura per AnzianiMinistero dell'Università e della Ricerca, ItaliaRecruiting
-
University of PittsburghCompletedAsthmaUnited States
-
Fundació Institut de Recerca de l'Hospital de la...UnknownPharmaceutical Care | Drug Related ProblemsSpain
-
University of Texas at AustinCompleted
-
Boston University Charles River CampusNational Institute of Mental Health (NIMH)CompletedSchizophrenia | Schizoaffective Disorder | Bipolar Disorder | Major Depression | Chronic Mental DisorderUnited States
-
Children's Hospital of PhiladelphiaNational Institute of Mental Health (NIMH); University of PennsylvaniaCompleted
-
Universidad Miguel Hernandez de ElcheNot yet recruitingCardiovascular Diseases | Coronary Disease | Chronic Disease | Secondary PreventionSpain
-
Gazi UniversityNot yet recruitingCaregivers With a Child Followed up With a Cancer DiagnosisTurkey
-
Children's Hospital of PhiladelphiaAgency for Healthcare Research and Quality (AHRQ); Devereux Center for Effective...Completed