Computerized Anxiety Sensitivity Treatment for Opioid Use Disorders (CAST-O)
Evaluating the Utility of a Brief Computerized Anxiety Sensitivity Intervention for Opioid Use Disorders: A Pilot Investigation
Přehled studie
Postavení
Postavení
Podmínky
Podmínky
Intervence / Léčba
Intervence / Léčba
Detailní popis
Typ studie
Typ studie
Zápis (Aktuální)
Zápis
Fáze
Fáze
- Nelze použít
Kontakty a umístění
Studijní místa
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Louisiana
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New Orleans, Louisiana, Spojené státy, 70119
- Southeast Louisiana Veterans Health Care System
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Kritéria účasti
Kritéria způsobilosti
Kritéria způsobilosti
Věk způsobilý ke studiu
Přijímá zdravé dobrovolníky
Pohlaví způsobilá ke studiu
Popis
Inclusion Criteria:
- Veterans must be diagnosed with an opioid use disorder
Exclusion Criteria:
- Less than 18 years of age
- Actively suicidal
- Actively psychotic
- Uncontrolled bipolar disorder (i.e., not stable on medications for at least one month)
Studijní plán
Jak je studie koncipována?
Detaily designu
- Primární účel: Léčba
- Přidělení: N/A
- Intervenční model: Přiřazení jedné skupiny
- Maskování: Žádné (otevřený štítek)
Počet zbraní
Zbraně a zásahy
Skupina účastníků / ArmSkupina účastníků / Arm |
Intervence / LéčbaIntervence / Léčba |
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Experimentální: Computerized Anxiety Sensitivity Treatment
CAST is a newly developed computerized intervention designed to closely model the educational and behavioral techniques that are commonly used in the treatment of anxiety and related conditions.The one time intervention takes approximately 45 minutes to complete.
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CAST is a newly developed computerized intervention designed to closely model the educational and behavioral techniques that are commonly used in the treatment of anxiety and related conditions.
A psychoeducation component focuses on the nature of anxiety and its effects on the mind and body.
Veterans will be taught that physiological and psychological arousal is not dangerous, although they may have developed a conditioned fear of this arousal.
Interoceptive exposure (IE) exercises will also be introduced to as a way to reduce or eliminate the conditioned fear response.
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Co je měření studie?
Primární výstupní opatření
Primární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
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Intervention Acceptability Questionnaire (IAQ)
Časové okno: One week post-intervention
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The IAQ is an 11-item self-report questionnaire designed to measure treatment satisfaction.
The IAQ includes nine items assessing acceptability (e.g., Do you think the information provided during the computerized intervention was helpful?
How likely are you to use the information and techniques you learned during the computerized intervention?), which are rated on a 4-point Likert-type scale (0 = no; 1 = somewhat; 2 = moderately; 3 = yes) and two free response items requesting suggestions for improving the treatment.
The IAQ will be administered at post-intervention to allow us to assess treatment acceptability.
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One week post-intervention
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Sekundární výstupní opatření
Sekundární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
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Alcohol Use Disorders Identification Test (AUDIT)
Časové okno: Baseline
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The AUDIT is a 10-item self-report questionnaire designed by the World Health Organization to classify individuals with alcohol-related problems.
The AUDIT will be administered at baseline for descriptive purposes.
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Baseline
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Drug Use Disorders Identification Test (DUDIT)
Časové okno: Baseline
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The DUDIT is an 11-item self-report questionnaire intended for use with the AUDIT as a way to classify individuals with drug-related problems.
The DUDIT will be administered at baseline for descriptive purposes
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Baseline
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PTSD Checklist for DSM-5 (PCL-5)
Časové okno: Baseline
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The PCL-5 is a 20-item self-report questionnaire designed to assess DSM-5 symptoms of PTSD.
The PCL-5 will be administered at baseline for descriptive purposes.
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Baseline
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Anxiety Sensitivity Index-3 (ASI-3)
Časové okno: Baseline, One week post-intervention, and Four weeks post-intervention
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The ASI-3 is an 18-item self-report questionnaire designed to measure fear of and concern about the negative effects of anxious arousal.
The ASI-3 will be administered at all timepoints to allow us to assess treatment-related changes in AS.
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Baseline, One week post-intervention, and Four weeks post-intervention
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Depression Anxiety Stress Scale (DASS)
Časové okno: Baseline, One week post-intervention, and Four weeks post-intervention
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The DASS is a 21-item self-report questionnaire assessing depression, anxiety, and stress symptoms.
The DASS will be administered at all timepoints to allow us to assess treatment-related changes in depression, anxiety, and stress symptoms.
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Baseline, One week post-intervention, and Four weeks post-intervention
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Depression Symptom Inventory-Suicide Subscale (DSI-SS)
Časové okno: Baseline, One week post-intervention, and Four weeks post-intervention
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The DSI-SS is a four-item self-report questionnaire designed to assess suicidal ideation, suicidal plans, control of suicidal thoughts, and suicidal impulses.
The DSI-SS will be administered at all timepoints to allow us to assess treatment-related changes in suicidality.
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Baseline, One week post-intervention, and Four weeks post-intervention
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Desires for Drug Questionnaire (DDQ)
Časové okno: Baseline, One week post-intervention, and Four weeks post-intervention
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The DDQ is a 13-item self-report questionnaire designed to measure instant (i.e., present moment) cravings associated with opioid use.
The DDQ will be administered at all timepoints to allow us to assess treatment-related changes in cravings.
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Baseline, One week post-intervention, and Four weeks post-intervention
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Obsessive Compulsive Drug Use Scale (OCDUS)
Časové okno: Baseline, One week post-intervention, and Four weeks post-intervention
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The OCDUS is a 12-item self-report questionnaire designed to assess heroin thoughts and interference, intention to use heroin and control of its consumption, and resistance against thoughts and decisions to use heroin.
The OCDUS will be administered at all timepoints to allow us to assess treatment related changes in thoughts and control over thoughts.
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Baseline, One week post-intervention, and Four weeks post-intervention
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Short Opiate Withdrawal Scale (SOWS)
Časové okno: Baseline, One week post-intervention, and Four weeks post-intervention
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The SOWS is a 10-item self-report questionnaire designed to assess various symptoms of opiate withdrawal.
The SOWS will be administered at all timepoints to allow us to assess treatment-related changes in withdrawal symptoms.
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Baseline, One week post-intervention, and Four weeks post-intervention
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Work and Social Adjustment Scale (WSAS)
Časové okno: Baseline, One week post-intervention, and Four weeks post-intervention
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The WSAS is a 5-item descriptive measure of subjective interference of psychiatric symptoms in various life domains (e.g., work, leisure, and family).
The WSAS will be administered at all timepoints to allow us to assess treatment-related changes in global life domains.
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Baseline, One week post-intervention, and Four weeks post-intervention
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Spolupracovníci a vyšetřovatelé
Sponzor
Sponzor
Spolupracovníci
Spolupracovníci
Vyšetřovatelé
Vyšetřovatelé
- Vrchní vyšetřovatel: Amanda M Raines, PhD, Southeast Louisiana Veterans Health Care System
Publikace a užitečné odkazy
Obecné publikace
- Bohnert AS, Valenstein M, Bair MJ, Ganoczy D, McCarthy JF, Ilgen MA, Blow FC. Association between opioid prescribing patterns and opioid overdose-related deaths. JAMA. 2011 Apr 6;305(13):1315-21. doi: 10.1001/jama.2011.370.
- Keough ME, Schmidt NB. Refinement of a brief anxiety sensitivity reduction intervention. J Consult Clin Psychol. 2012 Oct;80(5):766-72. doi: 10.1037/a0027961. Epub 2012 Apr 2.
- Schmidt NB, Capron DW, Raines AM, Allan NP. Randomized clinical trial evaluating the efficacy of a brief intervention targeting anxiety sensitivity cognitive concerns. J Consult Clin Psychol. 2014 Dec;82(6):1023-33. doi: 10.1037/a0036651. Epub 2014 May 12.
- Schmidt NB, Eggleston AM, Woolaway-Bickel K, Fitzpatrick KK, Vasey MW, Richey JA. Anxiety Sensitivity Amelioration Training (ASAT): a longitudinal primary prevention program targeting cognitive vulnerability. J Anxiety Disord. 2007;21(3):302-19. doi: 10.1016/j.janxdis.2006.06.002. Epub 2006 Aug 4.
- Hearon BA, Calkins AW, Halperin DM, McHugh RK, Murray HW, Otto MW. Anxiety sensitivity and illicit sedative use among opiate-dependent women and men. Am J Drug Alcohol Abuse. 2011 Jan;37(1):43-7. doi: 10.3109/00952990.2010.535581. Epub 2010 Nov 19. Erratum In: Am J Drug Alcohol Abuse. 2011 Jan;37(1):47.
- Bohnert AS, Ilgen MA, Galea S, McCarthy JF, Blow FC. Accidental poisoning mortality among patients in the Department of Veterans Affairs Health System. Med Care. 2011 Apr;49(4):393-6. doi: 10.1097/MLR.0b013e318202aa27.
- Veilleux JC, Colvin PJ, Anderson J, York C, Heinz AJ. A review of opioid dependence treatment: pharmacological and psychosocial interventions to treat opioid addiction. Clin Psychol Rev. 2010 Mar;30(2):155-66. doi: 10.1016/j.cpr.2009.10.006. Epub 2009 Oct 30.
- Reiss, S. and R. McNally, Expectancy model of fear, in Theoretical Issues in Behavior Therapy, S. Reiss and R. Bootzin, Editors. 1985, Academic Press: San Diego, CA. p. 107-122.
- Lejuez CW, Paulson A, Daughters SB, Bornovalova MA, Zvolensky MJ. The association between heroin use and anxiety sensitivity among inner-city individuals in residential drug use treatment. Behav Res Ther. 2006 May;44(5):667-77. doi: 10.1016/j.brat.2005.04.006. Epub 2005 Jul 5.
- Lejuez CW, Zvolensky MJ, Daughters SB, Bornovalova MA, Paulson A, Tull MT, Ettinger K, Otto MW. Anxiety sensitivity: a unique predictor of dropout among inner-city heroin and crack/cocaine users in residential substance use treatment. Behav Res Ther. 2008 Jul;46(7):811-8. doi: 10.1016/j.brat.2008.03.010. Epub 2008 Mar 28.
- Schmidt NB, Norr AM, Allan NP, Raines AM, Capron DW. A randomized clinical trial targeting anxiety sensitivity for patients with suicidal ideation. J Consult Clin Psychol. 2017 Jun;85(6):596-610. doi: 10.1037/ccp0000195. Epub 2017 Mar 13.
- Barlow, D.H., et al., Behavioral treatment of panic disorder. Behavior Therapy, 1989. 20(2): p. 261-282.
Termíny studijních záznamů
Hlavní termíny studia
Začátek studia (Aktuální)
Začátek studia
Primární dokončení (Aktuální)
Primární dokončení
Dokončení studie (Aktuální)
Dokončení studie
Termíny zápisu do studia
První předloženo
První předloženo
První předloženo, které splnilo kritéria kontroly kvality
První předloženo, které splnilo kritéria kontroly kvality
První zveřejněno (Aktuální)
První zveřejněno
Aktualizace studijních záznamů
Poslední zveřejněná aktualizace (Aktuální)
Poslední zveřejněná aktualizace
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
Naposledy ověřeno
Naposledy ověřeno
Více informací
Termíny související s touto studií
Klíčová slova
Další relevantní podmínky MeSH
Další identifikační čísla studie
Další identifikační čísla studie
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Studuje lékový produkt regulovaný americkým FDA
Studuje produkt zařízení regulovaný americkým úřadem FDA
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