Evaluation of a novel telemedicine-based intervention to manage body image disturbance in head and neck cancer survivors

被引:31
作者
Graboyes, Evan M. [1 ,2 ]
Maurer, Stacey [2 ,3 ]
Park, Yeonhee [2 ,4 ]
Marsh, Courtney H. [1 ]
McElligott, James T. [5 ]
Day, Terry A. [1 ]
Hornig, Joshua D. [1 ]
Sterba, Katherine R. [2 ,4 ]
机构
[1] Med Univ South Carolina, Dept Otolaryngol Head & Neck Surg, 135 Rutledge Ave,MSC 550, Charleston, SC 29425 USA
[2] Med Univ South Carolina, Hollings Canc Ctr, Charleston, SC 29425 USA
[3] Med Univ South Carolina, Dept Psychiat & Behav Sci, Charleston, SC 29425 USA
[4] Med Univ South Carolina, Dept Publ Hlth Sci, Charleston, SC 29425 USA
[5] Med Univ South Carolina, Dept Pediat, Charleston, SC 29425 USA
关键词
body image; cancer; cognitive-behavioral therapy; head and neck cancer; oncology; telemedicine; DISTRESS; SCALE;
D O I
10.1002/pon.5399
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives: 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. Methods: 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 postBRIGHT to assess its acceptability and clinical impact. Participants completed semistructured interviews to evaluate the feasibility and acceptability of BRIGHT and refine the intervention. Results: 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. Conclusions: 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.
引用
收藏
页码:1988 / 1994
页数:7
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