Questa pagina è stata tradotta automaticamente e l'accuratezza della traduzione non è garantita. Si prega di fare riferimento al Versione inglese per un testo di partenza.

Impact of Lifestyle Modification on the Development of Dementia, Chronic Kidney Disease, Diabetes, Chronic Obstructive Pulmonary Disease, Cancers and Cardiovascular Disease in a Thai General Population

30 maggio 2017 aggiornato da: P Chamnan, Sanpasitthiprasong Hospital

Impact of Lifestyle Modification on Prevention of Dementia, Chronic Kidney Disease, Diabetes, Chronic Obstructive Pulmonary Disease, Cancers and Cardiovascular Disease in a Thai General Population: Cluster Randomized Controlled Trial

This is a community-based cluster randomized control trial aimed to investigate the impact of lifestyle modification (diet, physical activity, alcohol drinking and smoking) on the development of dementia, diabetes, chronic kidney disease, cancers, chronic obstructive pulmonary disease and cardiovascular disease in an intermediate risk population in mixed urban-rural areas of Ubon Ratchathani.

Panoramica dello studio

Descrizione dettagliata

This is a community-based cluster randomized control trial aimed to investigate the impact of lifestyle modification (diet, physical activity, alcohol drinking and smoking) on the development of dementia, diabetes, chronic kidney disease, cancers, chronic obstructive pulmonary disease and cardiovascular disease in an intermediate risk population in mixed urban-rural areas of Ubon Ratchathani.

Objectives:

  1. examine the impact of lifestyle modification on the development of dementia, diabetes, chronic kidney disease, cancers, chronic obstructive pulmonary disease and cardiovascular disease in an intermediate risk population in Ubon Ratchathani
  2. examine the economic impact of lifestyle modification on prevention of dementia, diabetes, chronic kidney disease, cancers, chronic obstructive pulmonary disease and cardiovascular disease in an intermediate risk population in Ubon Ratchathani

Study design: community-based cluster randomized control trial

Setting: 60 villages randomly selected from mixed urban-rural areas in 15 districts of Ubon Ratchathani province.

Study population: 3,600 apparently healthy men and women aged 45-75 years who have resided in the village selected for at least one year. 4,000 men and women will be approached and screened.

Screening and baseline assessment:

After community consent, potential participants will be informed about the details of the project. For those who are willing to participate, written informed consent will be given before carrying out all research procedures. Participants will be questioned about their demographic characteristics, medical and family history, health behaviours including diet, physical activity, alcohol drinking and smoking. Physical activity will be assess using the Global Physical Activity Questionnaire (GPAQ) and diet will be assessed using 24 hour food recall. Their cognitive function will be assessed using the Mini-Mental State Exam (MMSE), Thai version, and clock drawing test and depression test will also be performed. Physical examination includes weight, height, blood pressure, waist and hip circumference as well as physical fitness test.

Fasting blood samples will be collected for the following laboratory tests: Complete blood count, creatinine, estimated glomerular filtration rate (eGFR), fasting plasma glucose, glycated haemoglobin (HbA1c), total cholesterol, triglyceride, HDL and estimated LDL-cholesterol, serum glutamic oxaloacetic transaminase (SGOT), serum glutamic pyruvic transaminase (SGPT), thyroid stimulating hormone (TSH), Ca++, PO4-, urine creatinine/albumin, urine sodium & potassium.

Interventions:

Participants in 30 villages in the intervention group will be given 4x4 lifestyle modification intervention, which will address four health behaviors (diet, physical activity, alcohol drinking and smoking) at four different levels: individual, household, knowledge management and community levels. A new computer program called 'iActive' will be used. The program was adapted from the GPAQ with add-on functions to allow real-time assessment and presentation of the energy expenditure along with recommendations specific to each individual. Dietary counseling will be given individually following assessment using a new dietary assessment program called Dietary Assessment Scanning Calculator (DISC). Home visit will be done every 3 months by responsible nurses and village health volunteers in order to assess and give simple counseling about health behaviors. Knowledge management will be undertaken through meetings and forums between participants and villages with support from trained nurses. Situation analysis and agreed community action will be encouraged to address community problems concerning four health behaviors. A combination of these intensive interventions will be given for 3 years.

Follow-up and outcome ascertainment:

Participants will be followed at 1, 2, 5 and 10 years after baseline assessment for the development of the outcomes of interest. In each follow-up, procedures identical to baseline assessment will be done.

Primary outcome: Incident dementia Incident dementia will be ascertained by a battery of screening test (MMSE, clock drawing and depression tests) and those with abnormal test results will be referred to neuro-medicine specialists at the regional hospital for further investigations and diagnosis.

Secondary outcomes:

  1. Type 2 diabetes mellitus
  2. chronic kidney disease
  3. cancers
  4. chronic obstructive pulmonary disease
  5. cardiovascular disease
  6. body mass index
  7. waist circumference
  8. blood pressure
  9. Fasting plasma glucose
  10. HbA1c
  11. Lipids (total cholesterol, triglyceride, HDL and estimated LDL)

Tertiary outcomes:

  1. MMSE scores or Cognitive decline
  2. Alzheimer's disease
  3. Physical activity levels
  4. Dietary intake
  5. prevalence of current smokers
  6. prevalence of alcohol consumption

Tipo di studio

Interventistico

Iscrizione (Anticipato)

3600

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.

Luoghi di studio

    • Ubon Ratchathani
      • Muaeng, Ubon Ratchathani, Tailandia, 34000
        • Sanpasitthiprasong Hospital

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 45 anni a 75 anni (Adulto, Adulto più anziano)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Descrizione

Inclusion Criteria:

  • Thai nationality
  • Age 45-75 years
  • Have resided in the Ubon Ratchathani's villages for at least 1 year
  • Those giving written informed consent to participate in the research project

Exclusion Criteria:

  • Known case of dementia, chronic kidney disease, diabetes, chronic obstructive pulmonary disease, cancers and cardiovascular disease
  • Unable to communicate well in Thai
  • Unable to move or get physical exercise
  • Those at risk of having complications from performing physical exercise
  • Those diagnosed with cancers of any system/ organ or those in the end of life period

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: Separare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Lifestyle modification
4 x 4 lifestyle modification intervention, addressing four health behaviors including physical activity, diet, smoking and alcohol drinking, at four different levels, i.e. individual, household, group/ knowledge management, and community levels
Participants in the intervention group will be given 4x4 lifestyle modification intervention, which will address four health behaviors (diet, physical activity, alcohol drinking and smoking) at four different levels: individual, household, knowledge management and community levels. A new computer program called 'iActive' adapted from the GPAQ with add-on functions to allow real-time assessment and presentation of the energy expenditure along with recommendations specific to each individual will be used. Dietary counseling will be given individually following assessment using a new dietary assessment program called Dietary Assessment Scanning Calculator. Home visit will be done every 3 months by responsible nurses and village health volunteers. Knowledge management will be done through meetings between participants and villages with support from trained nurses. Situation analysis and community action will be encouraged to address four health behaviors.
Nessun intervento: Control
No special intervention will be given. Prevention and treatment in normal practice is allowed

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Dementia
Lasso di tempo: 10 years
Number of participants with dementia. Incident dementia will be diagnosed by medical specialists (Neuro-Med) following a battery of screening tests, including mini-mental state exam, depression and clock drawing tests.
10 years

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Type 2 diabetes mellitus
Lasso di tempo: 3, 5 and 10 years
Number of participants with type 2 diabetes mellitus. Diabetes mellitus is biochemically and clinically diagnosed.
3, 5 and 10 years
Cardiovascular disease
Lasso di tempo: 5 and 10 years
Number of participants with cardiovascular disease. Clinical diagnosis of cardiovascular disease. Diagnostic information will be obtained from medical records review and service reimbursement data.
5 and 10 years
Cancers
Lasso di tempo: 5 and 10 years
Number of participants with cancers. Diagnostic information will be obtained from medical records review and service reimbursement data.
5 and 10 years
Chronic obstructive pulmonary disease
Lasso di tempo: 5 and 10 years
Number of participants with physician-diagnosed chronic obstructive pulmonary disease. Diagnostic information will be obtained from medical records review and service reimbursement data.
5 and 10 years
Mortality
Lasso di tempo: 5 and 10 years
All-cause mortality retrieved from death certificate database, which captures deaths nationwide, dates of death and related causes.
5 and 10 years
Blood sugar
Lasso di tempo: 1, 2, 5 and 10 years
Blood sugar assessed as fasting plasma glucose and glycated hemoglobin (HbA1c)
1, 2, 5 and 10 years
Blood lipids
Lasso di tempo: 1, 2, 5 and 10 years
Blood lipids include total, LDL- and HDL-cholesterol and triglyceride
1, 2, 5 and 10 years

Altre misure di risultato

Misura del risultato
Misura Descrizione
Lasso di tempo
Physical activity levels
Lasso di tempo: 1, 2, 5 and 10 years
Physical activity levels assessed using the global physical activity questionnaire (GPAQ)
1, 2, 5 and 10 years
Diet
Lasso di tempo: 1, 2, 5 and 10 years
Diet assessed by 24 hour food recall
1, 2, 5 and 10 years
Prevalence of current smokers
Lasso di tempo: 1, 2, 5 and 10 years
Percentage of current smokers in the study samples
1, 2, 5 and 10 years
Prevalence of alcohol consumption
Lasso di tempo: 1, 2, 5 and 10 years
Percentage of those who report alcohol consumption
1, 2, 5 and 10 years
Cognitive function
Lasso di tempo: 2, 5 and 10 years
Cognitive function assessed by MMSE score
2, 5 and 10 years

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Direttore dello studio: Prasert Boongird, MD, Dementia Association of Dementia
  • Investigatore principale: Parinya Chamnan, MD, PhD, Sanpasitthiprasong Hospital
  • Investigatore principale: Wannee Nitiyanant, MD, Siriraj Hospital
  • Investigatore principale: Wichai Aekplakorn, MD, PhD, Ramathibodi Hospital, Mahidol University
  • Investigatore principale: Chanida Pachotikarn, PhD, Thai Dietetic Society
  • Investigatore principale: Chaicharn Deerochanawong, MD, Rajvithi Hospital
  • Investigatore principale: Surasak Kantachuvesiri, MD, PhD, Ramathibodi Hospital, Mahidol University
  • Investigatore principale: Wallaya Jongjaroenprasert, MD, Ramathibodi Hospital, Mahidol University
  • Investigatore principale: Atiporn Ingsathit, MD, PhD, Ramathibodi Hospital, Mahidol University
  • Investigatore principale: Win Techakehakij, MD, PhD, Lampang Hospital
  • Investigatore principale: Phanida Krittayapoositpot, MD, Dementia Association of Thailand
  • Investigatore principale: Worawan Chailimpamontri, MD, Bhumibol Adulyadej Hospital
  • Investigatore principale: Ampika Mangklabruks, MD, Faculty of medicine, Chiangmai University

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

1 marzo 2016

Completamento primario (Anticipato)

1 marzo 2027

Completamento dello studio (Anticipato)

1 agosto 2027

Date di iscrizione allo studio

Primo inviato

16 novembre 2016

Primo inviato che soddisfa i criteri di controllo qualità

16 novembre 2016

Primo Inserito (Stima)

18 novembre 2016

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

31 maggio 2017

Ultimo aggiornamento inviato che soddisfa i criteri QC

30 maggio 2017

Ultimo verificato

1 maggio 2017

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • CMR-571
  • HSRI 59-069 (Altro numero di sovvenzione/finanziamento: Health System Research Institute)
  • TCTR20161116001 (Identificatore di registro: Thai Clinical Trials Registry)
  • 59-00-0228 (Altro numero di sovvenzione/finanziamento: Thai Health Promotion Foundation)

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 .

Sottoscrivi