Evaluation of a novel telemedicine-based intervention to manage body image disturbance in head and neck cancer survivors.
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| Title: | Evaluation of a novel telemedicine-based intervention to manage body image disturbance in head and neck cancer survivors. |
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| Authors: | Graboyes, Evan M. (AUTHOR), Maurer, Stacey (AUTHOR), Park, Yeonhee (AUTHOR), Marsh, Courtney H. (AUTHOR), McElligott, James T. (AUTHOR), Day, Terry A. (AUTHOR), Hornig, Joshua D. (AUTHOR), Sterba, Katherine R. (AUTHOR) |
| Source: | Psycho-Oncology. Dec2020, Vol. 29 Issue 12, p1988-1994. 7p. 1 Diagram, 3 Charts. |
| Subjects: | Body image disturbance, Head & neck cancer, Cancer survivors, Body image |
| Abstract: | |
| Copyright of Psycho-Oncology is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) | |
| Database: | Psychology and Behavioral Sciences Collection |
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| Abstract: | <bold>Objectives: </bold>The study aimed to evaluate the feasibility, acceptability, and preliminary clinical impact of BRIGHT (Building a Renewed ImaGe after Head & neck cancer Treatment), a novel telemedicine-based cognitive-behavioral intervention to manage body image disturbance (BID) in head and neck cancer (HNC) survivors.<bold>Methods: </bold>Head and neck cancer survivors with BID were enrolled into a single-arm pilot trial. Participants completed study measures at baseline, 1- and 3-months post-BRIGHT to assess its acceptability and clinical impact. Participants completed semi-structured interviews to evaluate the feasibility and acceptability of BRIGHT and refine the intervention.<bold>Results: </bold>Ten HNC survivors with BID were enrolled into the trial of tablet-based BRIGHT. BRIGHT was feasible, as judged by low dropout (n = 1), high session completion rates (100%; 45/45) and low rates of technical issues with the tablet-based delivery (11% minor; 0% major). Ninety percent of participants were highly likely to recommend BRIGHT, reflecting its acceptability. BRIGHT was associated with a 34.5% reduction in mean Body Image Scale scores at 1-month post-BRIGHT (mean difference from baseline = 4.56; 95% CI 1.55, 7.56), an effect that was durable at 3-months post-BRIGHT (mean decrease from baseline = 3.56; 95% CI 1.15-5.96). Program evaluation revealed high levels of satisfaction with BRIGHT, particularly the delivery platform. During the qualitative evaluation, participants highlighted that BRIGHT improved image-related coping behavior.<bold>Conclusions: </bold>BRIGHT is feasible, acceptable to HNC survivors, and has significant potential as a novel approach to manage BID in HNC survivors. Additional research is necessary to refine BRIGHT and evaluate its clinical efficacy and scalability. [ABSTRACT FROM AUTHOR] |
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| ISSN: | 10579249 |
| DOI: | 10.1002/pon.5399 |