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Cocaine abstinence during the “critical period” of a contingency management trial predicts future abstinence in people with cocaine use disorder

Producción científica: Articlerevisión exhaustiva

4 Citas (Scopus)

Resumen

Background: Contingency Management (CM) is being piloted as a treatment for stimulant use disorder in several US states, highlighting the need for treatment optimization. One important goal of optimization is decreasing drug use during the early stages of treatment, which has predicted success in other interventions. However, this “critical period” has not been reported in CM trials. The purpose of this analysis was to determine if, after accounting for baseline abstinence and incentive condition, abstinence in a CM trial for people with Cocaine Use Disorder (CUD) could be predicted by cocaine use during a first-week critical period. Methods: Eighty-seven participants with CUD were randomized to receive contingent high or low value incentives for cocaine abstinence or were in a non-contingent control group. Generalized estimating equations (GEE) were used to analyze urine test results over 36 timepoints during the 12-week intervention. To assess for a critical period, the first three visits were included in the GEE as a covariate for remaining urine test results. Results: Participants who provided more negative samples during the critical period were significantly more likely to produce a negative urine sample during the remainder of the trial, though some effects of group remained after controlling for the critical period. Conclusions: These results indicate that a critical period exists for CM trials, and it can explain a substantial amount of future performance. Early contact with an abstinence-contingent high magnitude alternative reinforcer may explain additional performance beyond the critical period, further justifying the use of high magnitude alternative reinforcers.

Idioma originalEnglish
Número de artículo111030
PublicaciónDrug and Alcohol Dependence
Volumen253
DOI
EstadoPublished - dic 1 2023

Nota bibliográfica

Publisher Copyright:
© 2023 Elsevier B.V.

Financiación

This research was supported by grants from the National Institute on Drug Abuse ( R01DA043938 ; NCT03224546 ). Sean Regnier’s time on this project was supported by grants from the National Institute on Drug Abuse ( T32DA035200 ; TL1TR001997 ) of the National Institutes of Health . Thomas Shellenberg’s time on this project was support by grants from the National Institute on Drug Abuse ( T32DA035200 , R01DA047368 , R01DA045023 ). The funding agencies had no role in study design, data collection or analysis, or preparation and submission of the manuscript. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.

FinanciadoresNúmero del financiador
National Institutes of Health (NIH)R01DA047368, R01DA045023
National Institute on Drug AbuseNCT03224546, TL1TR001997, R01DA043938, T32DA035200

    ODS de las Naciones Unidas

    Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible

    1. Good health and well being
      Good health and well being

    ASJC Scopus subject areas

    • Toxicology
    • Pharmacology
    • Psychiatry and Mental health
    • Pharmacology (medical)

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