Ohio State University Comprehensive Cancer Center
Columbus, Ohio, 43210, United States
NCT Number: NCT06582030
This clinical trial evaluates the impact of a Stop Addiction Stigma (SAS) training workshop with a short description of the conditions related to addiction (vignettes) on stigmatizing attitudes toward individuals with substance abuse disorders. Reviews have shown that patients with substance abuse disorders have experienced negative attitudes from their health care providers. Negative attitudes may lead to less involvement from the provider and the patient and may lead to less effective care. Using case vignettes with a SAS workshop may be an effective method to help people learn about addiction, reduce the stigma toward addiction and improve the quality of health care.
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Notify Me18 year and older
All sexes
Interventional
Not applicable
Columbus, Ohio, 43210, United States
PRIMARY OBJECTIVE:
I. To describe the impact of SAS training on participants' responses to people with a substance impairment.
SECONDARY OBJECTIVES:
I. To evaluate the feasibility of stigma training workshops on stigmatizing attitudes health care personnel.
II. To explore the maintainability of responses over time. III. To explore relationships between language and stigmatizing attitudes.
OUTLINE: Participants are randomized to 1 of 6 group case vignettes.
GROUP A (CHRONICALLY RELAPSING BRAIN DISEASE): Participants view the chronically relapsing brain disease vignette and attend a SAS workshop on study.
GROUP B (BRAIN DISEASE): Participants view the brain disease vignette and attend a SAS workshop on study.
GROUP C (DISEASE): Participants view the disease vignette and attend a SAS workshop on study.
GROUP D (ILLNESS): Participants view the illness vignette and attend a SAS workshop on study.
GROUP E (DISORDER): Participants view the disorder vignette and attend a SAS workshop on study.
GROUP F (PROBLEM): Participants view the problem vignette and attend a SAS workshop on study.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Ancillary studies
Other names: Assess, Study Assessment, Study Observation
View the chronically relapsing brain disease vignette
Attend a SAS workshop
Other names: Training Programs
Time frame: Before, immediately after and 8 weeks after the session
Stigmatizing attitudes will be measured with the Stigma and Attribution Assessment. The assessment score will be compared both between and within participants for each case vignette. Results will be reported with descriptive statistics, including means and standard deviations or medians and first-third quartiles for continuous variables, and frequencies and percentages for discrete variables.The linear mixed effect model will be used to study the repeated stigma and attribution measures over time (pre-workshop, immediately post-workshop, and 8 weeks post-workshop) within 6 vignettes as well as the effects between the vignettes, while controlling for the potential confounding factors (e.g., sex).
Time frame: At 90 minute session.
The proportion of participants attending the workshop will be summarized with 95% confidence interval.
Time frame: Before, immediately following and 8 weeks after the session.
The proportion of participants who respond to the post-workshop evaluations will be summarized with 95% confidence interval.
Ohio State University Comprehensive Cancer Center
Other
Stop Addiction Stigma Training Workshop With Case Vignettes to Decrease Stigmatizing Attitudes Toward People With Substance Abuse Disorders
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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