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Binge Drinking Among Youngs is a Risk Factor for Alcohol Use Disorders

24. februar 2017 opdateret af: Giovanni Addolorato, Catholic University of the Sacred Heart

Binge Drinking Among Young Students is a Risk Factor for the Development of Alcohol Use Disorders: Results From an Epidemiologic-observational Study

The purpose of this study was to assess drinking habits and patterns of alcohol consumption, smoking habits, use of illicit drugs and the prevalence of binge drinking and alcohol use disorders among Italian young students. Furthermore to investigate the correlation between binge drinking and alcohol use disorders.

Studieoversigt

Status

Afsluttet

Betingelser

Detaljeret beskrivelse

This study was performed on 2,704 subjects attending high school, through the administration of questionnaires regarding socio-demographic data, anthropometric characteristics, pattern and amount of alcohol intake, smoking habits, use of illicit drugs and physical activity were administered to students. Moreover mood and anxiety were evaluated through AUDIT, STAI-Y1, STAY-Y2 and ZUNG. The aim of the study was to assess drinking habits and patterns of alcohol consumption, smoking habits, use of illicit drugs and the prevalence of binge drinking and alcohol use disorders among Italian young students. Furthermore to investigate the correlation between binge drinking and alcohol use disorders.

Undersøgelsestype

Observationel

Tilmelding (Faktiske)

2704

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

13 år til 19 år (Barn, Voksen)

Tager imod sunde frivillige

Ja

Køn, der er berettiget til at studere

Alle

Prøveudtagningsmetode

Sandsynlighedsprøve

Studiebefolkning

2,704 subjects attending high school in three italian cities

Beskrivelse

Inclusion Criteria:

  • Subjects attending high school of three italian cities (Rome, Latina, Frosinone)
  • Subjects aged between 13 and 19 years
  • Subjects that accept the interview

Exclusion Criteria:

  • Subjects that don't accept the interview

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Binge drinking behavior
Tidsramme: 1 year
Binge drinking behavior was defined as an alcohol consumption of more than 5 drinks within about two hour period
1 year

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Amount of alcoholic beverage consumed
Tidsramme: 1 year
One drink is defined as an amount of alcoholic beverages containing 12 g of absolute alcoho
1 year
Type of alcoholic beverage consumed
Tidsramme: 1 year
1 year
Frequency of alcohol consumption
Tidsramme: 1 year
1 year
Alcohol consumption outside meals
Tidsramme: 1 year
One drink is defined as an amount of alcoholic beverages containing 12 g of absolute alcoho
1 year
Frequency of alcohol drinking outside meals
Tidsramme: 1 year
One drink is defined as an amount of alcoholic beverages containing 12 g of absolute alcoho
1 year
Amount of cigarettes smoked
Tidsramme: 1 year
1 year
Frequency of cigarettes smoked
Tidsramme: 1 year
1 year
Type of illicit drugs used
Tidsramme: 1 year
1 year
Frequency of illicit drugs used
Tidsramme: 1 year
1 year
Diagnosis of Alcohol Use Disorder
Tidsramme: 1 year
According AUDIT score
1 year
STAI score
Tidsramme: 1 year
STAI assess existing anxiety a predisposition to anxious reaction as a personality characteristic. Itis structuredby two axes (y1 for state anxiety and y2 for trait anxiety), both consisting of 20 multiple-choice items; each item has a score from 1 to 4; the total score of y1 and y 2 axes can range from 20 to 80. This test was selected for simplicity, validity and reliability. The subjects evaluated were divided as high and low anxious and a value of 40 was used to distinguish the two groups
1 year
Zung-SDS
Tidsramme: 1 year
Zung-SDS constitutes an effective instrument in screening for depression and its positive predictive value of a diagnosis of depression is between 88.7% and 92.3%. The Zung-SDS contains 20 multiple items with a score from 1 to 4 each; total score above 50 indicates a condition of depression
1 year

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Sponsor

Catholic University of the Sacred Heart

Efterforskere

  • Ledende efterforsker: Giovanni Addolorato, MD, Catholic University of Sacred Heart, Rome

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. januar 2015

Primær færdiggørelse (Faktiske)

1. juni 2015

Studieafslutning (Faktiske)

1. juni 2015

Datoer for studieregistrering

Først indsendt

14. december 2016

Først indsendt, der opfyldte QC-kriterier

20. februar 2017

Først opslået (Faktiske)

23. februar 2017

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

27. februar 2017

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

24. februar 2017

Sidst verificeret

1. januar 2017

Mere information

Begreber relateret til denne undersøgelse

Yderligere relevante MeSH-vilkår

Andre undersøgelses-id-numre

  • BingeDrinkingamongYoungStudy

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

INGEN

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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Betingelser

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Placeringer

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