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Effect of Cognitive Behavioral Therapy for Insomnia on Alcohol Treatment Outcomes Among US Veterans: A Randomized Clinical Trial.
Miller, Mary Beth; Carpenter, Ryan W; Freeman, Lindsey K; Dunsiger, Shira; McGeary, John E; Borsari, Brian; McCrae, Christina S; Arnedt, J Todd; Korte, Paul; Merrill, Jennifer E; Carey, Kate B; Metrik, Jane.
Afiliação
  • Miller MB; University of Missouri, Columbia.
  • Carpenter RW; University of Missouri-St Louis, St Louis.
  • Freeman LK; University of Missouri, Columbia.
  • Dunsiger S; Brown University School of Public Health, Providence, Rhode Island.
  • McGeary JE; Brown University School of Public Health, Providence, Rhode Island.
  • Borsari B; Providence VA Medical Center, Providence, Rhode Island.
  • McCrae CS; San Francisco VA Health Care System, San Francisco, California.
  • Arnedt JT; University of California, San Francisco.
  • Korte P; University of South Florida College of Nursing, Tampa.
  • Merrill JE; University of Michigan School of Medicine, Ann Arbor.
  • Carey KB; Harry S. Truman Memorial Veterans' Hospital, Columbia, Missouri.
  • Metrik J; Brown University School of Public Health, Providence, Rhode Island.
JAMA Psychiatry ; 80(9): 905-913, 2023 09 01.
Article em En | MEDLINE | ID: mdl-37342036
ABSTRACT
Importance Three of 4 adults in treatment for alcohol use disorder (AUD) report symptoms of insomnia. Yet the first-line treatment for insomnia (cognitive behavioral therapy for insomnia, CBT-I) is often delayed until abstinence is established.

Objective:

To test the feasibility, acceptability, and preliminary efficacy of CBT-I among veterans early in their AUD treatment and to examine improvement in insomnia as a mechanism for improvement in alcohol use outcomes. Design, Setting, and

Participants:

For this randomized clinical trial, participants were recruited through the Addictions Treatment Program at a Veterans Health Administration hospital between 2019 and 2022. Patients in treatment for AUD were eligible if they met criteria for insomnia disorder and reported alcohol use in the past 2 months at baseline. Follow-up visits occurred posttreatment and at 6 weeks.

Interventions:

Participants were randomly assigned to receive 5 weekly sessions of CBT-I or a single session about sleep hygiene (control). Participants were asked to complete sleep diaries for 7 days at each assessment. Main Outcomes and

Measures:

Primary outcomes included posttreatment insomnia severity (assessed using the Insomnia Severity Index) and follow-up frequency of any drinking and heavy drinking (4 drinks for women, ≥5 drinks for men; number of days via Timeline Followback) and alcohol-related problems (Short Inventory of Problems). Posttreatment insomnia severity was tested as a mediator of CBT-I effects on alcohol use outcomes at the 6-week follow-up.

Results:

The study cohort included 67 veterans with a mean (SD) age of 46.3 years (11.8); 61 (91%) were male and 6 (9%) female. The CBT-I group included 32 participants, and the sleep hygiene control group 35 participants. Of those randomized, 59 (88%) provided posttreatment or follow-up data (31 CBT-I, 28 sleep hygiene). Relative to sleep hygiene, CBT-I participants reported greater decreases in insomnia severity at posttreatment (group × time interaction -3.70; 95% CI, -6.79 to -0.61) and follow-up (-3.34; 95% CI, -6.46 to -0.23) and greater improvements in sleep efficiency (posttreatment, 8.31; 95% CI, 1.35 to 15.26; follow-up, 18.03; 95% CI, 10.46 to 25.60). They also reported greater decreases in alcohol problems at follow-up (group × time interaction -0.84; 95% CI, -1.66 to -0.02), and this effect was mediated by posttreatment change in insomnia severity. No group differences emerged for abstinence or heavy-drinking frequency. Conclusions and Relevance In this randomized clinical trial, CBT-I outperformed sleep hygiene in reducing insomnia symptoms and alcohol-related problems over time but had no effect on frequency of heavy drinking. CBT-I should be considered a first-line treatment for insomnia, regardless of abstinence. Trial Registration ClinicalTrials.gov Identifier NCT03806491.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Veteranos / Terapia Cognitivo-Comportamental / Alcoolismo / Distúrbios do Início e da Manutenção do Sono Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Veteranos / Terapia Cognitivo-Comportamental / Alcoolismo / Distúrbios do Início e da Manutenção do Sono Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2023 Tipo de documento: Article