- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT04828655
Analysis of Bioparametric Measures for Correlating Daily Habits and Reducing Blood Pressure
Análisis de Medidas bioparamétricas Para Correlacionar Los hábitos Diarios y Reducir la tensión Arterial
Panoramica dello studio
Stato
Condizioni
Descrizione dettagliata
In the Valencian Community, 93% of deaths appear to be related to (non-communicable) diseases such as: obesity, hypertension and diabetes. In 2013, cardiovascular diseases were the leading cause of death in women (34.4%) and the second in men (28.0%). There is a forecast that overweight and obesity will reach levels of 89% and 85% in men and women, respectively, by 2030. This will result in an increase in the obesity-related prevalence of coronary heart disease by 97%. The promotion of research on arterial hypertension and how it could be reduced is one of the basic pillars in decreasing the prevalence and incidence in the Spanish population. Research should anticipate and develop treatments and vaccines that prevent new scenarios of widespread infection.
Therefore, the main objective is to study the effects of the use of a mobile application plus recommendations based on a Mediterranean diet on the intake of micronutrients from natural sources (not drugs) on health indicators, cardiovascular parameters (blood pressure...), physical condition and body composition in the adult Spanish population.
Tipo di studio
Iscrizione (Effettivo)
Fase
- Non applicabile
Contatti e Sedi
Luoghi di studio
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-
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Alicante, Spagna, 03690
- Alejandro Martínez Rodríguez
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
Inclusion Criteria:
- Over 40 years old
- Healthy.
- Blood pressure levels slightly elevated but less than 140 mm Hg and/or diastolic pressure less than 90 mm Hg.
- Smartphone access
Exclusion Criteria:
- Subjects with diseases.
- Consumption of drugs and/or supplements.
- Subjects with food intolerances/allergies.
- Subjects with muscle or joint injury.
- Subjects with impossibility to follow up the intervention.
- Refusal of informed consent
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Prevenzione
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione incrociata
- Mascheramento: Separare
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Nessun intervento: CONTROL GROUP
Recommendations on healthy eating habits based on the Mediterranean diet and moderate physical activity.
Specific micronutrient intake focused on improving cardiovascular parameters and body composition.
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|
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Sperimentale: EXPERIMENTAL GROUP
Recommendations on healthy eating habits based on the Mediterranean diet and moderate physical activity through an application based on machine learning.
Intake of specific micronutrients focused on improving cardiovascular parameters and body composition.
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Specific diet program and moderate physical activity, all guided and mediated by a mobile application.
As well as the recording and monitoring of periodic evaluations of health indicators.
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Cardiovascular variables; heart rate.
Lasso di tempo: 9 months
|
Heart rate measurement done with an activity wristband.
|
9 months
|
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Cardiovascular variables; blood pressure.
Lasso di tempo: 9 months
|
Measurement of blood pressure (systolic and diastolic) with a digital tensiometer.
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9 months
|
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Physical condition; time.
Lasso di tempo: 9 months
|
The evaluation of the physical condition will be carried out by means of the mile test, in which the subjects have to cover this distance walking, and in the shortest possible time.
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9 months
|
|
Body Composition - Bioimpedance
Lasso di tempo: 9 months
|
Assessment of body composition using the TANITA (Tokyo, Japan) validated bioimpedance scale to obtain the results of fat mass, fat-free mass and visceral mass.
|
9 months
|
|
Weight
Lasso di tempo: 9 months
|
The weight of the subjects will be obtained using the TANITA (Tokyo, Japan).
From the body mass and height data, the BMI (kg/m2) will be obtained.
|
9 months
|
|
Height
Lasso di tempo: 9 months
|
The height of the subjects will be measured with the SECA 123 stadiometer (Hamburg, Germany).
From the body mass and height data, the BMI (kg/m2) will be obtained.
|
9 months
|
|
Body Composition - Skinfolds
Lasso di tempo: 9 months
|
The kinanthropometric assessment will be carried out using the methodology proposed for the restricted profile by the International Society for the Development of Kineanthropometry (ISAK).
The material used to measure skinfolds will be a plicometer.
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9 months
|
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Body Composition - Perimeters
Lasso di tempo: 9 months
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The kinanthropometric assessment will be carried out using the methodology proposed for the restricted profile by the International Society for the Development of Kineanthropometry (ISAK).
The material used to measure perimeters will be a tape.
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9 months
|
|
Body Composition - Diameters
Lasso di tempo: 9 months
|
The kinanthropometric assessment will be carried out using the methodology proposed for the restricted profile by the International Society for the Development of Kineanthropometry (ISAK).
The material used to measure diameters will be a pachymeter.
|
9 months
|
Collaboratori e investigatori
Sponsor
Investigatori
- Investigatore principale: Alejandro Martínez Rodríguez, Alicante University
Studiare le date dei record
Studia le date principali
Inizio studio (Effettivo)
Completamento primario (Effettivo)
Completamento dello studio (Effettivo)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- UA-2020-04-16
Piano per i dati dei singoli partecipanti (IPD)
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Informazioni su farmaci e dispositivi, documenti di studio
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