慢性皮肤病成年患者的自我污名化:HautKompass网络项目的开发及其可用性、可接受性和可行性的试点测试。

Self-Stigma in Adults Living With Chronic Skin Disease: Development of the HautKompass Web-Based Program and Pilot Test of Its Usability, Acceptability, and Feasibility.

作者信息

Traxler Juliane, Stuhlmann Caroline F Z, da Silva Burger Neuza, Stierle Christian, Djamei Vahid, Darzina Anna, Rudnik Marie, Sommer Rachel

机构信息

1, German Center for Health Services Research in Dermatology, Institute for Health Services Research in Dermatology and Nursing, University Medical Center Hamburg-Eppendorf, Martinistraße 52, Hamburg, 20246, Germany, 49 40 7410 54207.

Psychology School, Hochschule Fresenius, Hamburg, Germany.

出版信息

JMIR Form Res. 2025 May 22;9:e70290. doi: 10.2196/70290.

Abstract

BACKGROUND

Self-stigma is common among people with chronic skin disease and can substantially impair quality of life and psychosocial well-being. Few interventions targeting skin disease-related self-stigma are available, especially in Germany.

OBJECTIVE

This pilot study aims to develop a web-based self-guided program to reduce self-stigma among people with chronic skin disease, and test its usability, acceptability, and feasibility.

METHODS

We developed the HautKompass program based on 2 systematic literature reviews and the expertise from psychodermatologists and patients. Its usability, acceptability, and feasibility were tested among adults with psoriasis, atopic dermatitis, hidradenitis suppurativa, alopecia areata, and vitiligo. After completing the program, participants provided feedback on each session and on their overall experience using the Client Satisfaction Questionnaire and study-specific feedback items. The program was considered feasible if the dropout rate was below 40% and participants spent 45 minutes or less per session. Data were analyzed descriptively.

RESULTS

HautKompass is grounded in compassion-focused therapy and cognitive behavioral therapy and consists of 8 self-guided sessions. Of the 41 persons who provided informed consent and filled in the screening questionnaire, 29 were eligible for participation. A total of 27 participants started the program and 20 completed all sessions and the posttest questionnaire. Results indicated high usability (mean 26.12, SD 6.13; on a scale ranging from 8-32) and acceptability (mean 17.41, SD 3.12; on a scale ranging from 5-20). Users rated the program as helpful, the psychoeducation and exercise instructions as comprehensible, and the extent of the program as adequate. Criticism concerned the length of some sessions, the electronic voice used in exercises, and some of the examples being too "general" or "cliché." Regarding feasibility, the program's extent was deemed adequate, participants spent substantially less time on the individual sessions (mean 16.9, SD 4.4 minutes) than the predefined criterion and few participants dropped out after starting the program (n=7, 26%), indicating low barriers. Importantly, the majority of users dropped out within the first 2 sessions, possibly due to the slightly longer duration and focus on theory, or due to unmet expectations, highlighting areas for improvement.

CONCLUSIONS

Overall, HautKompass was found to be a usable, acceptable program with feasible implementation. Limitations of this pilot study include not testing accessibility for people with disabilities and the small, relatively young, and mostly female sample, which limits the generalizability of the findings. The feedback obtained was used to revise the program and the recruitment strategy prior to testing its effectiveness in a randomized controlled trial. If HautKompass is found to be effective in reducing skin disease-related self-stigma, it will be made widely available to improve psychosocial care for people with chronic skin disease and could be adapted for other skin diseases and visible differences in general.

摘要

背景

自我污名化在慢性皮肤病患者中很常见,会严重损害生活质量和心理社会幸福感。针对皮肤病相关自我污名化的干预措施很少,尤其是在德国。

目的

本试点研究旨在开发一个基于网络的自我引导项目,以减少慢性皮肤病患者的自我污名化,并测试其可用性、可接受性和可行性。

方法

我们基于两项系统文献综述以及心理皮肤科医生和患者的专业知识开发了HautKompass项目。在患有银屑病、特应性皮炎、化脓性汗腺炎、斑秃和白癜风的成年人中测试了其可用性、可接受性和可行性。完成项目后,参与者使用客户满意度问卷和特定研究反馈项目对每个环节以及他们的总体体验提供反馈。如果辍学率低于40%且参与者每个环节花费45分钟或更少时间,则该项目被认为是可行的。对数据进行描述性分析。

结果

HautKompass基于以同情为中心的疗法和认知行为疗法,由8个自我引导环节组成。在41名提供知情同意并填写筛查问卷的人中,29人符合参与条件。共有27名参与者开始该项目,20人完成了所有环节和测试后问卷。结果表明可用性高(平均26.12,标准差6.13;范围为8 - 32)和可接受性高(平均17.41,标准差3.12;范围为5 - 20)。用户认为该项目有帮助,心理教育和练习指导易于理解,项目内容适当。批评意见涉及一些环节的长度、练习中使用的电子语音以及一些例子过于“笼统”或“陈词滥调”。关于可行性,该项目的内容被认为是适当的,参与者在各个环节上花费的时间(平均16.9,标准差4.4分钟)大大少于预定义标准,并且很少有参与者在开始项目后退出(n = 7,26%),表明障碍较低。重要的是,大多数用户在前两个环节内退出,可能是因为时间稍长且侧重于理论,或者是因为期望未得到满足,这突出了需要改进的方面。

结论

总体而言,HautKompass被认为是一个可用、可接受且实施可行的项目。本试点研究的局限性包括未测试对残疾人的可及性,以及样本量小、相对年轻且大多为女性,这限制了研究结果的普遍性。所获得的反馈被用于在随机对照试验中测试其有效性之前修订项目和招募策略。如果发现HautKompass在减少皮肤病相关自我污名化方面有效,它将被广泛提供以改善对慢性皮肤病患者的心理社会护理,并且可能适用于其他皮肤病和一般的可见差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6866/12141763/1644f5f9dc7a/formative-v9-e70290-g001.jpg

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