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    A preventive intervention to modify depression risk targets after breast cancer diagnosis: Design and single-arm pilot study

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    Author
    Weihs, Karen L.
    McConnell, Mairead H.
    Wiley, Joshua F.
    Crespi, Catherine M.
    Sauer-Zavala, Shannon
    Stanton, Annette L.
    Affiliation
    Univ Arizona, Dept Psychiat
    Univ Arizona, Dept Psychol
    Issue Date
    2019-04
    Keywords
    breast cancer
    coping
    depression
    intervention
    oncology
    prevention
    
    Metadata
    Show full item record
    Publisher
    WILEY
    Citation
    Weihs, K. L., McConnell, M. H., Wiley, J. F., Crespi, C. M., Sauer‐Zavala, S., & Stanton, A. L. (2019). A preventive intervention to modify depression risk targets after breast cancer diagnosis: Design and single‐arm pilot study. Psycho‐Oncology.
    Journal
    PSYCHO-ONCOLOGY
    Rights
    © 2019 John Wiley & Sons, Ltd.
    Collection Information
    This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.
    Abstract
    Objective Apply the National Institutes of Health (NIH) Stage Model to design and test an intervention to prevent depression in breast cancer patients at risk for depression. Methods We identified mindful emotion awareness, along with approach and avoidance strategies for cancer-related coping and emotion regulation, as targets for a preventive intervention adapted from the Unified Protocol for Transdiagnostic Treatment of Emotional Disorders. Patients' preferences for individual, in-person, and time-efficient sessions informed the design. Patients at risk for depression received a 6-week, 5-hour intervention with daily exercises. Intervention targets were assessed at baseline, before each session, and 4-weeks post intervention. Mixed effects analysis of variance (ANOVA) assessed change over the follow-up period, controlling for age, partnered status, and disease stage. Results Fifty-five percent (40/72) of women screened within 6 months of diagnosis had elevated depression risk. Of these, 24 (60%) signed consent. Sixteen received intervention after five were excluded for current depressive disorder, cognitive impairment, or death. Three dropped out. Ninety-eight percent attendance and 77% practice days indicated feasibility. Effect sizes (Cohen's d) corrected for regression to the mean (RTM) were 0.82 for cancer-related acceptance coping, 0.65 for cancer-related emotional expression, and 0.32 and 0.42 for decreased cancer-related avoidance coping and depressive symptoms, respectively. Effect sizes for variables lacking data to correct for RTM were 1.0, 0.7, and 0.5 for decreased rumination, experiential avoidance, and fear of depression, respectively, and 1.3, 0.6, and 0.4 for increased cognitive flexibility, distress tolerance, and describing/not judging emotions, respectively. Conclusions The feasibility of this intervention and malleability of its targets support its further investigation.
    Note
    12 month embargo; first published: 25 February 2019
    ISSN
    1057-9249
    1099-1611
    DOI
    10.1002/pon.v28.4
    Version
    Final accepted manuscript
    Sponsors
    Breast Cancer Research Fund [20184915]; National Cancer Institute [NIH R01 CA133081, NCI-NIH P30 CA 16042, NCI-NIH P30CA023074]
    Additional Links
    https://onlinelibrary.wiley.com/toc/10991611/28/4
    ae974a485f413a2113503eed53cd6c53
    10.1002/pon.v28.4
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