- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT04064281
The Healthy Cantonese Diet on Cardiometabolic Syndrome
19 agosto 2019 aggiornato da: Huilian Zhu, Sun Yat-sen University
Effect of the Healthy Cantonese Diet on Cardiometabolic Syndrome in Chinese Adults
The DASH diet (Dietary Approaches to Stop Hypertension) have been proven to lower risk of cardiovascular diseases.
But the DASH diet is inconsistent with Chinese dietary pattern.
In this study, based on the typical Cantonese diet, the healthy Cantonese diet is developed according to the DASH diet and the balanced dietary pattern of the Chinese Dietary Guidelines 2016.
The randomized control trial is designed to investigate whether the healthy Cantonese diet has benefit to blood pressure, blood lipid, blood glucose and other cardiometabolic biomarkers among adults with cardiometabolic syndrome in Guangdong, China.
Panoramica dello studio
Stato
Sconosciuto
Condizioni
Intervento / Trattamento
Tipo di studio
Interventistico
Iscrizione (Anticipato)
90
Fase
- Non applicabile
Contatti e Sedi
Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.
Criteri di partecipazione
I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.
Criteri di ammissibilità
Età idonea allo studio
Da 25 anni a 75 anni (Adulto, Adulto più anziano)
Accetta volontari sani
No
Sessi ammissibili allo studio
Tutto
Descrizione
Inclusion Criteria:
- Age 25-75 years old, male or female;
- have lived in this community for the past six months, and have no plans to move out or go out in the next three months;
- the systolic blood pressure is within 130-159mmHg regardless of medication.
- maintaining the current medication (mainly drugs for hypertension, diabetes or hyperlipidemia) throughout the research period, with the category and dose unchanged;
- the number of test meal consumed is no less than 18;
- community feeding mode: eat a meal at least once a day at the research center (preferably lunch or dinner); or home delivery mode: upload meal pictures for three meals every day, and eat a meal and have physical examination at the research center at least once a week;
- sign the informed consent form.
Exclusion Criteria:
- fasting blood glucose ≥10.0mmol/L;
- total cholesterol ≥7.2mmol/L;
- injected inulin within a month;
- unwilling or unable to change the original dietary pattern, or have special dietary needs (such as vegetarians);
- alcoholism;
- BMI ≥30kg/m^2, or losing weight currently;
- have acute cardiovascular and cerebrovascular events occurred in the past six months;
- have a history of chronic kidney disease, intestinal irritation or asthma;
- women who have been/are preparing for pregnancy or lactation;
- in combination with other serious diseases such as cancer, chronic heart failure, severe depression or other mental disorders, long-term bedridden or unable to move freely;
- have a history of common food allergies (eggs, seafood, peanuts, etc.);
- have undergone gastrointestinal surgery;
- currently suffering from acute phase of diseases such as respiratory infections, fever, severe diarrhea;
- have deaf-mutism, dementia, unable to communicate properly.
Piano di studio
Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Prevenzione
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Doppio
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
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Sperimentale: the healthy Cantonese diet
Based on the typical Cantonese diet, the healthy Cantonese diet is developed according to the DASH diet and the balanced dietary pattern of the Chinese Dietary Guidelines 2016.
In this diet, the main nutrients, dietary fiber, sodium, calcium, magnesium and potassium are set to achieve the healthy goal.
Compared with the typical Cantonese diet, the healthy Cantonese diet is increased in fruit, vegetables, low-fat dairy products, whole grains, nuts and seeds, and reduced in salt, oil and sweets.
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After a 1-week run-in period, the intervention group will eat the healthy Cantonese diet for 4 consecutive weeks.
Free meals will be provided 3 times a day (breakfast, lunch, dinner).
The actually intake of every meal for all subjects will be recorded to estimate their nutrients intake.
All subjects will be advised to avoid eating other food, but they should inform researchers of what they eat if they eat food that we will not provide.
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Comparatore placebo: the typical Cantonese diet
The typical Cantonese diet is a diet of what many Cantonese eat.
In this diet, the main nutrients, dietary fiber, sodium, calcium, magnesium and potassium are set at the average dietary intake levels in Guangdong.
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After a 1-week run-in period, the control group will still eat the typical Cantonese diet for 4 consecutive weeks.
Free meals will be provided 3 times a day (breakfast, lunch, dinner).
The actually intake of every meal for all subjects will be recorded to estimate their nutrients intake.
All subjects will be advised to avoid eating other food, but they should inform researchers of what they eat if they eat food that we will not provide.
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Metabolic syndrome score
Lasso di tempo: before and after 4-week intervention
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Changes of metabolic syndrome score in healthy Cantonese diet compared with changes of typical Cantonese diet.
Metabolic syndrome score will be derived by standardizing and then summing the following continuously distributed indices of adiposity (waist circumference) to create a z score: hypertension (the average of systolic blood pressure and diastolic blood pressure); hyperglycaemia (fasting plasma glucose); insulin resistance (fasting insulin); fasting HDL-cholesterol × -1; and fasting triacylglycerol z score.
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before and after 4-week intervention
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Systolic blood pressure and diastolic blood pressure
Lasso di tempo: before and after 4-week intervention
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Changes of systolic blood pressure and diastolic blood pressure in healthy Cantonese diet compared with changes of typical Cantonese diet.
Blood pressure will be measured by trained investigator at baseline, week 1, week 2, week 3 and week 4, and systolic blood pressure and diastolic blood pressure will be recorded.
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before and after 4-week intervention
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Blood lipid profile
Lasso di tempo: before and after 4-week intervention
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Changes of blood lipid profile in healthy Cantonese diet compared with changes of typical Cantonese diet.
Blood lipid profile (total cholesterol, TC; triglyceride, TG; LDL cholesterol, LDLc; HDL cholesterol, HDLc) will be tested by a validated biomedical analyses laboratory using vein serum at baseline and week 4.
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before and after 4-week intervention
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Glucose metabolism
Lasso di tempo: before and after 4-week intervention
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Changes of glucose metabolism in healthy Cantonese diet compared with changes of typical Cantonese diet.
Glucose metabolism (fasting plasma glucose and fasting insulin) will be tested by a validated biomedical analyses laboratory using vein serum at baseline and week 4 and insulin resistance index (HOMA-IR) will be calculated by [fasting insulin (mU/L) × fasting plasma glucose (mmol/L) ]/22.5.
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before and after 4-week intervention
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Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Blood biochemical marker
Lasso di tempo: before and after 4-week intervention
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Changes of blood biochemical marker in healthy Cantonese diet compared with changes of typical Cantonese diet.
Blood biochemical marker (calcium, potassium, sodium, magnesium and phosphorus in mmol/L; uric acid in μmol/L) will be tested by a validated biomedical analyses laboratory using vein serum at baseline and week 4.
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before and after 4-week intervention
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Urinary sodium and potassium
Lasso di tempo: before and after 4-week intervention
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Changes of urinary sodium and potassium in healthy Cantonese diet compared with changes of typical Cantonese diet.
Urinary sodium and potassium will be tested by a validated biomedical analyses laboratory using morning urine at baseline and week 4.
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before and after 4-week intervention
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Intestinal microbiota composition
Lasso di tempo: before and after 4-week intervention
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Changes of intestinal microbiota composition in healthy Cantonese diet compared with changes of typical Cantonese diet.
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before and after 4-week intervention
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Gut microbial gene richness
Lasso di tempo: before and after 4-week intervention
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Changes of gut microbial gene richness in healthy Cantonese diet compared with changes of typical Cantonese diet.
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before and after 4-week intervention
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Inflammatory biomarkers
Lasso di tempo: before and after 4-week intervention
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Changes of inflammatory biomarkers in healthy Cantonese diet compared with changes of typical Cantonese diet.
Inflammatory biomarkers (CRP in mg/L; Tumor TNF-α and IL-6 in ng/L) will be tested by a validated biomedical analyses laboratory using vein serum at baseline and week 4.
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before and after 4-week intervention
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Cardiopulmonary function
Lasso di tempo: before and after 4-week intervention
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Changes of cardiopulmonary function in healthy Cantonese diet compared with changes of typical Cantonese diet.
Cardiopulmonary function will be measured by cardiopulmonary exercise testing using CORTEX MetaLyzer 3B at baseline and week 4.
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before and after 4-week intervention
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Endothelial function
Lasso di tempo: before and after 4-week intervention
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Changes of endothelial function in healthy Cantonese diet compared with changes of typical Cantonese diet.
Flow-mediated dilatation (FMD) will be assessed to evaluate endothelial function by using UNEX EF38G at baseline and week 4.
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before and after 4-week intervention
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Body composition
Lasso di tempo: before and after 4-week intervention
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Changes of body composition in healthy Cantonese diet compared with changes of typical Cantonese diet.
Body composition will be tested by using dual energy X-ray absorptiometry at baseline and week 4.
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before and after 4-week intervention
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Body mass index (BMI)
Lasso di tempo: before and after 4-week intervention
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Height in meters and weight in kilograms will be combined to report body mass index (BMI) in kg/m^2.
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before and after 4-week intervention
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Ratio of waist to hip circumference (WHR)
Lasso di tempo: before and after 4-week intervention
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Waist circumference in centimeters and hip circumference in centimeters will be combined to report ratio of waist to hip circumference (WHR).
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before and after 4-week intervention
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Collaboratori e investigatori
Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.
Sponsor
Studiare le date dei record
Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.
Studia le date principali
Inizio studio (Anticipato)
1 settembre 2019
Completamento primario (Anticipato)
31 dicembre 2021
Completamento dello studio (Anticipato)
31 dicembre 2022
Date di iscrizione allo studio
Primo inviato
12 agosto 2019
Primo inviato che soddisfa i criteri di controllo qualità
19 agosto 2019
Primo Inserito (Effettivo)
21 agosto 2019
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
21 agosto 2019
Ultimo aggiornamento inviato che soddisfa i criteri QC
19 agosto 2019
Ultimo verificato
1 agosto 2019
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- CC-2019-03
Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
No
Studia un dispositivo regolamentato dalla FDA degli Stati Uniti
No
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
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