- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT02458131
Community-based Adolescent Diabetes Prevention Program
TEEN HEED: An Adolescent Peer Led Diabetes Prevention Intervention
Studieoversigt
Detaljeret beskrivelse
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiesteder
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New York
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New York, New York, Forenede Stater, 10029
- Icahn School of Medicine at Mount Sinai
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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria for pre-diabetes screening:
- Adolescents ages 13-19 years of age
- English speaking
Residents of East Harlem or members of an East Harlem Institution. Membership in an East Harlem institution includes the following:
- attending a school in East Harlem
- attending an after school or recreational activity in East Harlem
- receiving health care in East Harlem Proof of address or membership in an East Harlem institution will not be asked.
- At risk for diabetes (overweight/obese based on measured BMI percentile and with either a parent or grandparent with type 2 diabetes)
- No plans to relocate from New York City in the next year
Note: additional inclusion criteria for participation in workshops include diagnosis of pre-diabetes based on oral glucose tolerance test
Exclusion Criteria for pre-diabetes screening:
- <13 or >19 years of age
- Previous diagnosis of diabetes
- BMI percentile <85th percentile for age and gender based on Centers for Disease Control and Prevention definition
- Currently pregnant
- Speaking a language other than English
- On medications that may raise or lower blood sugar
- Plans to relocate from New York City within one year of enrollment-
Note: additional exclusion criteria for participation in workshops include fingerstick glucoses outside the pre-diabetes range during oral glucose tolerance testing and any cognitive or physical impairment that would preclude comprehension of the group educational program
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Forebyggelse
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
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Eksperimentel: TEEN HEED
Adolescent pre-diabetics will receive 8-12 weekly peer-led diabetes prevention educational workshops in community sites.
The in-person group workshops will be supplemented by support through mobile health technologies such as text messaging and social media.
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Peer-led workshops will cover behavioral skills including goal setting, self-monitoring, problem solving, contingency management, coping skills, and social support.
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Ingen indgriben: Wait List Control
Adolescent pre-diabetics in this group will not receive any intervention until collection of all follow up data and will then be offered the same intervention as the participants in the experimental arm.
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Change in body mass index (BMI)
Tidsramme: Baseline and 3 months
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Change in BMI at post-intervention (approximately 3 months) as compared to baseline
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Baseline and 3 months
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Change in BMI
Tidsramme: Baseline and 1 year
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Change in BMI at 1 year as compared to baseline
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Baseline and 1 year
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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Change in fasting blood glucose levels
Tidsramme: Baseline and 3 months
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Change in fasting blood glucose levels at post-intervention (approximately 3 months) as compared to baseline
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Baseline and 3 months
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Change in fasting blood glucose levels
Tidsramme: Baseline and 1 year
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Change in fasting blood glucose levels at 1 year as compared to baseline
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Baseline and 1 year
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Change in post prandial blood glucose level
Tidsramme: Baseline and 3 months
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Change in post prandial blood glucose level at post-intervention (approximately 3 months) as compared to baseline
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Baseline and 3 months
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Change in post prandial blood glucose level
Tidsramme: Baseline and 1 year
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Change in post prandial blood glucose level at 1 year as compared to baseline
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Baseline and 1 year
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Change in blood pressure
Tidsramme: Baseline and 3 months
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Change in blood pressure at post-intervention (approximately 3 months) as compared to baseline
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Baseline and 3 months
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Change in blood pressure
Tidsramme: Baseline and 1 year
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Change in blood pressure at 1 year as compared to baseline
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Baseline and 1 year
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Change in percent body fat
Tidsramme: Baseline and 3 months
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Change in percent body fat at post-intervention (approximately 3 months) as compared to baseline
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Baseline and 3 months
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Change in percent body fat
Tidsramme: Baseline and 1 year
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Change in percent body fat at 1 year as compared to baseline
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Baseline and 1 year
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Change in waist circumference
Tidsramme: Baseline and 3 months
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Change in waist circumference at post-intervention (approximately 3 months) as compared to baseline
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Baseline and 3 months
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Change in waist circumference
Tidsramme: Baseline and 1 year
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Change in waist circumference at 1 year as compared to baseline
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Baseline and 1 year
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Change in knowledge, attitudes, beliefs and behaviors related to diabetes and weight loss
Tidsramme: Baseline and 3 months
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Change in knowledge, attitudes, beliefs and behaviors (from the TEEN HEED survey) at post-intervention (approximately 3 months) as compared to baseline
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Baseline and 3 months
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Change in knowledge, attitudes, beliefs and behaviors related to diabetes and weight loss
Tidsramme: Baseline and 1 year
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Change in knowledge, attitudes, beliefs and behaviors (from the TEEN HEED survey) at 1 year as compared to baseline
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Baseline and 1 year
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Samarbejdspartnere og efterforskere
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Nita Vangeepuram, MD, MPH, Icahn School of Medicine at Mount Sinai
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Skøn)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- GCO 13-0901
- 5K23DK101692-02 (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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