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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. Mai 2017 aktualisiert von: 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.

Studienübersicht

Detaillierte Beschreibung

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

Studientyp

Interventionell

Einschreibung (Voraussichtlich)

3600

Phase

  • Unzutreffend

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienorte

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

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

45 Jahre bis 75 Jahre (Erwachsene, Älterer Erwachsener)

Akzeptiert gesunde Freiwillige

Nein

Studienberechtigte Geschlechter

Alle

Beschreibung

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

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Verhütung
  • Zuteilung: Zufällig
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Single

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: 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.
Kein Eingriff: Control
No special intervention will be given. Prevention and treatment in normal practice is allowed

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Dementia
Zeitfenster: 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

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Type 2 diabetes mellitus
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 1, 2, 5 and 10 years
Blood lipids include total, LDL- and HDL-cholesterol and triglyceride
1, 2, 5 and 10 years

Andere Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Physical activity levels
Zeitfenster: 1, 2, 5 and 10 years
Physical activity levels assessed using the global physical activity questionnaire (GPAQ)
1, 2, 5 and 10 years
Diet
Zeitfenster: 1, 2, 5 and 10 years
Diet assessed by 24 hour food recall
1, 2, 5 and 10 years
Prevalence of current smokers
Zeitfenster: 1, 2, 5 and 10 years
Percentage of current smokers in the study samples
1, 2, 5 and 10 years
Prevalence of alcohol consumption
Zeitfenster: 1, 2, 5 and 10 years
Percentage of those who report alcohol consumption
1, 2, 5 and 10 years
Cognitive function
Zeitfenster: 2, 5 and 10 years
Cognitive function assessed by MMSE score
2, 5 and 10 years

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Ermittler

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

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn

1. März 2016

Primärer Abschluss (Voraussichtlich)

1. März 2027

Studienabschluss (Voraussichtlich)

1. August 2027

Studienanmeldedaten

Zuerst eingereicht

16. November 2016

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

16. November 2016

Zuerst gepostet (Schätzen)

18. November 2016

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

31. Mai 2017

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

30. Mai 2017

Zuletzt verifiziert

1. Mai 2017

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

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