- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT01886716
Retraining Attention to Treat Alcohol Dependence and Social Anxiety (AMP)
15. december 2016 opdateret af: Joshua Magee, University of Cincinnati
Cognitive Bias Modification: A Novel Intervention for Alcohol Dependence and Social Anxiety
The purpose of this research is to test a computerized intervention for people with co-occurring social anxiety and alcohol dependence.
The intervention seeks to reduce symptoms by shifting attention away from alcohol-relevant and/or socially threatening cues.
The investigators expect that participants receiving alcohol or anxiety training will experience reductions in those specific symptoms compared to participants in a control condition.
The investigators also expect that participants receiving combined alcohol and anxiety training will show the largest reductions in alcohol and anxiety symptoms, relative to participants in any other condition.
Studieoversigt
Status
Afsluttet
Betingelser
Detaljeret beskrivelse
Alcohol Use Disorders (AUDs) and Social Anxiety Disorder are disabling and chronic conditions.
In spite of these common and significantly overlapping problems, insight into the mechanisms linking alcohol dependence and social anxiety symptoms is minimal, and there are not well established treatment guidelines for this population.
In this study, the investigators seek to develop a computerized intervention for individuals with symptoms of social anxiety and alcohol dependence.
The intervention attempts to reduce symptoms by shifting attention away from alcohol-relevant and/or socially threatening cues.
The investigators expect that participants receiving alcohol or anxiety training will experience reductions in those specific symptoms compared to participants in a control condition.
The investigators also expect that participants receiving combined alcohol and anxiety training will show the largest reductions in alcohol and anxiety symptoms, relative to participants in any other condition.
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
115
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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Ohio
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Cincinnati, Ohio, Forenede Stater, 45206
- University of Cincinnati Department of Family and Community Medicine
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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
18 år og ældre (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- Current alcohol dependence
- Elevated social anxiety symptoms
- Willingness to consider cutting down on drinking
Exclusion Criteria:
- Current psychosis
- Unmanaged manic symptoms
- Significant cognitive impairment
- Other drug use in past month
- Receiving cognitive behavioral therapy for alcohol use disorder or social anxiety
- Unable to read
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Dobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
---|---|
Eksperimentel: Anxiety Attention Training only
Participants will receive Anxiety Attention Training and placebo Alcohol training.
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Anxiety Attention Training will preferentially direct participants' attention away from reminders of anxiety.
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Eksperimentel: Alcohol Attention Training only
Participants will receive Alcohol Attention Training and placebo Anxiety training.
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Alcohol Attention Training will preferentially direct participants' attention away from reminders of alcohol.
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Eksperimentel: Anxiety + Alcohol Attention Training
Participants will receive both Anxiety Attention Training and Alcohol Attention Training.
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Anxiety Attention Training will preferentially direct participants' attention away from reminders of anxiety.
Alcohol Attention Training will preferentially direct participants' attention away from reminders of alcohol.
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Placebo komparator: Control Training
Participants will receive placebo Anxiety Training and placebo Alcohol training.
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Placebo Anxiety Training and Placebo Alcohol Training will not preferentially direct participants' attention away from reminders of anxiety or alcohol.
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
Liebowitz Social Anxiety Scale
Tidsramme: Baseline, weekly throughout the 4-week trial, and in the follow-up sessions (1 week and 1 month follow-ups)
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The experimenter-administered Liebowitz Social Anxiety Scale (Liebowitz, 1987) was the primary measure to assess social anxiety symptoms.
This well-validated instrument assesses fear and avoidance across a range of 24 social and performance situations during the course of the previous week.
A total LSAS score was computed, ranging from 0 (no fear or avoidance) to 144 (the greatest level of fear and avoidance).
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Baseline, weekly throughout the 4-week trial, and in the follow-up sessions (1 week and 1 month follow-ups)
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The Daily Drinking Questionnaire
Tidsramme: Baseline, weekly throughout the 4-week trial, and in the follow-up sessions (1 week and 1 month follow-ups)
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The Daily Drinking Questionnaire (Collins, Parks, & Marlatt, 1985) was the primary measure used to assess weekly alcohol consumption.
This calendar-based measure was administered by the experimenter once per week to monitor changes in symptoms.
The measure assessed the total number of drinks in the past week.
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Baseline, weekly throughout the 4-week trial, and in the follow-up sessions (1 week and 1 month follow-ups)
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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: Joshua C Magee, Ph.D., University of Cincinnati
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. juli 2013
Primær færdiggørelse (Faktiske)
1. december 2014
Studieafslutning (Faktiske)
1. december 2014
Datoer for studieregistrering
Først indsendt
17. juni 2013
Først indsendt, der opfyldte QC-kriterier
21. juni 2013
Først opslået (Skøn)
26. juni 2013
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
28. december 2016
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
15. december 2016
Sidst verificeret
1. december 2016
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 1R21AA021151 (U.S. NIH-bevilling/kontrakt)
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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