Noah R Wolkowicz, Brian Pittman, Shannon W Schrader, Danielle M Wesolowicz, Mehmet Sofuoglu, Alicia A Heapy, R Ross MacLean
{"title":"Cognitive bias modification for individuals with opioid use disorder and chronic pain did not predict changes in clinical outcomes.","authors":"Noah R Wolkowicz, Brian Pittman, Shannon W Schrader, Danielle M Wesolowicz, Mehmet Sofuoglu, Alicia A Heapy, R Ross MacLean","doi":"10.15288/jsad.25-00057","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>Attentional bias (AB), defined as the preferential focus on personally salient-compared to neutral-cues, has a hypothesized link to substance use disorders and chronic pain. While growing research demonstrates Cognitive Bias Modification (CBM) can alter ABs, evidence assessing the extent to which such alterations predict changes in clinical symptoms or behaviors (e.g., pain severity, craving) is lacking.</p><p><strong>Method: </strong>Secondary analysis of a clinical trial examining the feasibility, acceptability, and preliminary effectiveness of a 4-week CBM adjunct for veterans (<i>N</i>=28) receiving medication treatment for OUD (mOUD) with moderate pain for the past 3-months (MacLean et al., 2024; NCT04132609). We examined CBM effects vs. control on pain severity, interference, and catastrophizing, as well as opioid craving and withdrawal.</p><p><strong>Results: </strong>CBM for opioid and pain cues did not correspond with changes in the primary clinical outcomes of opioid craving and pain intensity, <i>p</i>'s ≥ .111. Additional analyses of other possible outcomes including pain interference, pain catastrophizing, and subjective opioid withdrawal were also not associated with CBM, <i>p</i>'s ≥ .125.</p><p><strong>Conclusions: </strong>Results from this pilot study did not show changes in pain severity or opioid craving corresponding to CBM for opioid and pain. Findings should be considered preliminary given our small sample size, however, findings indicate a distinction between ABs, their modification, and clinically salient outcomes. Future research should examine CBM in larger, more diverse samples and assess the impacts of addiction severity, substance type, naturalistic settings, and the use of more engaging methodologies (e.g., gamification of CBM tasks, using gaze-contingent paradigms).</p>","PeriodicalId":17159,"journal":{"name":"Journal of studies on alcohol and drugs","volume":" ","pages":""},"PeriodicalIF":2.4000,"publicationDate":"2025-06-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of studies on alcohol and drugs","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.15288/jsad.25-00057","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PSYCHOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Objective: Attentional bias (AB), defined as the preferential focus on personally salient-compared to neutral-cues, has a hypothesized link to substance use disorders and chronic pain. While growing research demonstrates Cognitive Bias Modification (CBM) can alter ABs, evidence assessing the extent to which such alterations predict changes in clinical symptoms or behaviors (e.g., pain severity, craving) is lacking.
Method: Secondary analysis of a clinical trial examining the feasibility, acceptability, and preliminary effectiveness of a 4-week CBM adjunct for veterans (N=28) receiving medication treatment for OUD (mOUD) with moderate pain for the past 3-months (MacLean et al., 2024; NCT04132609). We examined CBM effects vs. control on pain severity, interference, and catastrophizing, as well as opioid craving and withdrawal.
Results: CBM for opioid and pain cues did not correspond with changes in the primary clinical outcomes of opioid craving and pain intensity, p's ≥ .111. Additional analyses of other possible outcomes including pain interference, pain catastrophizing, and subjective opioid withdrawal were also not associated with CBM, p's ≥ .125.
Conclusions: Results from this pilot study did not show changes in pain severity or opioid craving corresponding to CBM for opioid and pain. Findings should be considered preliminary given our small sample size, however, findings indicate a distinction between ABs, their modification, and clinically salient outcomes. Future research should examine CBM in larger, more diverse samples and assess the impacts of addiction severity, substance type, naturalistic settings, and the use of more engaging methodologies (e.g., gamification of CBM tasks, using gaze-contingent paradigms).
期刊介绍:
The Journal of Studies on Alcohol and Drugs began in 1940 as the Quarterly Journal of Studies on Alcohol. It was founded by Howard W. Haggard, M.D., director of Yale University’s Laboratory of Applied Physiology. Dr. Haggard was a physiologist studying the effects of alcohol on the body, and he started the Journal as a way to publish the increasing amount of research on alcohol use, abuse, and treatment that emerged from Yale and other institutions in the years following the repeal of Prohibition in 1933. In addition to original research, the Journal also published abstracts summarizing other published documents dealing with alcohol. At Yale, Dr. Haggard built a large team of alcohol researchers within the Laboratory of Applied Physiology—including E.M. Jellinek, who became managing editor of the Journal in 1941. In 1943, to bring together the various alcohol research projects conducted by the Laboratory, Dr. Haggard formed the Section of Studies on Alcohol, which also became home to the Journal and its editorial staff. In 1950, the Section was renamed the Center of Alcohol Studies.