- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT01084928
A Culturally Tailored Lifestyle Intervention to Prevent Diabetes in South Asians (SHAPE)
24. september 2013 opdateret af: Venkat Narayan, Emory University
The South Asian Community, people with origins in India, Pakistan, Bangladesh, Maldives, Nepal, Sri Lanka, or Bhutan, are more likely to get diabetes, get diabetes at younger ages, and do worse health-wise once they have diabetes than the general population.
This study will test the feasibility and community acceptability of a culturally appropriate lifestyle intervention for the prevention of diabetes in the South Asian community.
The outcomes of this project could be used to plan larger interventions to prevent diabetes in South Asians, a rapidly growing segment of the US population.
Studieoversigt
Status
Afsluttet
Intervention / Behandling
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
16
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
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Georgia
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Atlanta, Georgia, Forenede Stater, 30322
- Emory University
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Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
25 år og ældre (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- Self-identified as being of South Asian origin
- Live in or near Atlanta, Georgia
- BMI greater than 22 kg/m2 calculated from standardized weight and height measurements (a BMI of greater than 22 kg/m2 is indicative of overweight in the South Asian population)
- A confirmed age greater than or equal to 25 determined by checking a valid photo identification (driver's license, passport, etc.)
- No prior diabetes diagnosis (physician diagnosis or on diabetes medication)
- A high risk of developing diabetes (pre-diabetes) as defined by a casual capillary glucose greater than or equal to 120 (measured during screening)
- Fasting glucose of 100-125 mg/dL (impaired fasting glucose tolerance) and/or 2-hour post-load glucose of 140-199 mg/dL (impaired glucose tolerance), measured at baseline visit
- No history of heart disease, serious illness, or conditions that may impede or prohibit participation and are not currently pregnant
Exclusion Criteria:
- Capillary glucose less than 120
- Fasting glucose less than 100 mg/dL or greater than 125 mg/dL OR 2 hour post-load glucose less than 140 mg/dL or greater than 199 mg/dL
- Age less than 25 years
- BMI less than 22 kg/m2
- Pregnancy
- History of heart disease or diabetes (other than gestational diabetes)
- Current functional difficulties
- Severe lung disease or cancer
- Failure to pass cardiovascular stress test
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Forebyggelse
- Tildeling: N/A
- Interventionel model: Enkelt gruppeopgave
- Maskning: Enkelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
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Eksperimentel: Intervention Arm (Diet and Exercise)
The lifestyle intervention will include a 16-week intervention period, followed by an 8 week, less intensive maintenance period.
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The intervention will be based on the Diabetes Prevention Program but tailored to the needs of the community based on feedback gathered in focus groups.
Classes will be group-based and will use a variety of teaching techniques and group-based work to teach participants about behavior change, diet, and physical activity.
Participant will be required to attend one group exercise class per week based on traditional Indian dances and other culturally appropriate activities.
In order to reach their weekly exercise goal of 150 minutes or more per week, participants will also be able to attend an additional group exercise class, an organized group walk, do a culturally-tailored work out video created by the study staff, and/or exercise on their own.
Andre navne:
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
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body weight
Tidsramme: 24 weeks (16 week intervention, 8 week maintenance)
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24 weeks (16 week intervention, 8 week maintenance)
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Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
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percent body fat
Tidsramme: 24 weeks (16 week intervention, 8 week maintenance)
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24 weeks (16 week intervention, 8 week maintenance)
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body mass index
Tidsramme: 24 weeks (16 week intervention, 8 week maintenance)
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24 weeks (16 week intervention, 8 week maintenance)
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waist-to-hip ratio
Tidsramme: 24 weeks (16 week intervention, 8 week maintenance)
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24 weeks (16 week intervention, 8 week maintenance)
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fasting glucose
Tidsramme: 24 weeks (16 week intervention, 8 week maintenance)
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24 weeks (16 week intervention, 8 week maintenance)
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blood pressure
Tidsramme: 24 weeks (16 week intervention, 8 week maintenance)
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24 weeks (16 week intervention, 8 week maintenance)
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plasma lipids
Tidsramme: 24 weeks (16 week intervention, 8 week maintenance)
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24 weeks (16 week intervention, 8 week maintenance)
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self-reported physical activity
Tidsramme: 24 weeks (16 week intervention, 8 week maintenance)
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24 weeks (16 week intervention, 8 week maintenance)
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Percent of Total Calories from Fat
Tidsramme: 24 weeks (16 week intervention, 8 week maintenance)
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24 weeks (16 week intervention, 8 week maintenance)
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Venkat Narayan, MD, PhD, Emory University
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart
1. april 2010
Primær færdiggørelse (Faktiske)
1. juli 2012
Studieafslutning (Faktiske)
1. juli 2012
Datoer for studieregistrering
Først indsendt
1. marts 2010
Først indsendt, der opfyldte QC-kriterier
9. marts 2010
Først opslået (Skøn)
11. marts 2010
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
25. september 2013
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
24. september 2013
Sidst verificeret
1. september 2013
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- IRB00035893
- 1R34DK081723-01A1 (U.S. NIH-bevilling/kontrakt)
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
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