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Integrating cognitive bias modification for pain and opioid cues into medication for opioid use disorder clinical care: Feasibility, acceptability, and preliminary results.
MacLean, R Ross; Heapy, Alicia A; Waters, Andrew J; Wolkowicz, Noah; Szollosy, Sara K; Meyerovich, Julia; Sofuoglu, Mehmet.
Afiliação
  • MacLean RR; VA Connecticut Healthcare System, West Haven, CT, USA; Yale University School of Medicine, New Haven, CT, USA. Electronic address: ross.maclean@yale.edu.
  • Heapy AA; VA Connecticut Healthcare System, West Haven, CT, USA; Yale University School of Medicine, New Haven, CT, USA.
  • Waters AJ; Uniformed Services University of the Health Sciences, Bethesda, MD, USA.
  • Wolkowicz N; VA Connecticut Healthcare System, West Haven, CT, USA; Yale University School of Medicine, New Haven, CT, USA.
  • Szollosy SK; VA Connecticut Healthcare System, West Haven, CT, USA.
  • Meyerovich J; VA Connecticut Healthcare System, West Haven, CT, USA; Yale University School of Medicine, New Haven, CT, USA.
  • Sofuoglu M; VA Connecticut Healthcare System, West Haven, CT, USA; Yale University School of Medicine, New Haven, CT, USA.
Drug Alcohol Depend ; 246: 109857, 2023 05 01.
Article em En | MEDLINE | ID: mdl-37004461
ABSTRACT

BACKGROUND:

Despite high co-occurrence, chronic pain is often unaddressed in treatment for opioid use disorder (OUD) and little is known about mechanisms that may underlie associations between pain and opioid use. Using an attentional bias (AB) task with both pain and opioid cues, we evaluated a cognitive bias modification (CBM) task administered during regularly scheduled medications for OUD (mOUD) dosing visits. The current study evaluated the feasibility, acceptability, and preliminary efficacy of the CBM task. Outcomes for AB tasks used traditional mean-based score and trial-level bias scores (TLBS).

METHODS:

In a double-blind, randomized controlled trial, 28 individuals with OUD and chronic pain engaged in mOUD were randomized to either CBM or an AB control condition and completed up to three tasks per week for four weeks. Standard AB task was completed at baseline and post-treatment. Participants completed feasibility and acceptability measures, and preliminary efficacy (i.e., change in AB) was assessed using ANOVA models.

RESULTS:

Participants attended 83.3% of scheduled sessions and generally reported the task was enjoyable, credible, and easy to complete. Preliminary results demonstrated a condition by time interaction highlighting a reduction in AB in the CBM group but not the control group in opioid TLBS variability (F[1,26]=5.01, p = .034) and pain TLBS towards (F[1,26]=6.42, p = .018) and pain TLBS variability (F[1,26]=5.24, p = .03).

CONCLUSIONS:

The current study supports integrating brief, computer-based tasks designed to reduce AB into mOUD clinical care. The preliminary results suggest that TLBS outcomes may be more sensitive to capture changes in AB; however, larger studies are required.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Buprenorfina / Dor Crônica / Transtornos Relacionados ao Uso de Opioides Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Humans Idioma: En Revista: Drug Alcohol Depend Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Buprenorfina / Dor Crônica / Transtornos Relacionados ao Uso de Opioides Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Humans Idioma: En Revista: Drug Alcohol Depend Ano de publicação: 2023 Tipo de documento: Article