在一项针对银屑病患者的概念验证前试验中,探索为期 7 周的心率变异生物反馈方案对皮肤严重程度、生活质量和心理健康的影响

CAND Journal Pub Date : 2024-03-21 DOI:10.54434/candj.151
S. Park, Devon Fox, Lee Young, Maya Roth, Baljit Khamba
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摘要

背景:银屑病通常与精神障碍和生活质量(QoL)下降并存,治疗方法通常忽视了疾病对心理的影响。心率变异性生物反馈疗法(HRVB)可通过提供自律神经功能的实时反馈,教导患者通过控制呼吸来管理压力,从而提供一种身心解决方案:研究为期 7 周的 HRVB 方案对银屑病患者的皮肤严重程度(SS)、生活质量和心理健康(MH)的影响,并确定干预后结果的可持续性:在加利福尼亚州圣迭戈的巴斯蒂尔大学诊所开展了一项单臂、概念验证前-后试验。共招募、筛选了五名患者,并对其进行了为期七周的 HRVB 方案治疗。评估包括通过牛皮癣面积和严重程度指数(PASI-P 和 PASI-C)进行的 SS 评估、通过卡迪夫皮肤病生活质量指数(DLQI)进行的 QoL 评估,以及通过广泛性焦虑症-7(GAD-7)和患者健康问卷-9(PHQ-9)进行的 MH 评估。数据收集点为基线、协议后和 1 个月的随访:结果:从基线到方案实施后,PASI-P、DLQI 和 GAD-7 均有明显改善。GAD-7 在基线和随访期间仍有明显变化。PASI-C和PHQ-9在任何时间范围内均未发现重大差异,其他量表在方案后和随访期间保持一致:结论:HRVB有望在7周内改善患者的SS、QoL和焦虑感。进一步的研究应扩大参与人数并使初始评分多样化,同时将 HRVB 与对照组进行比较:试验注册:ClinicalTrials.gov NCT05506644,2022年8月16日回顾性注册。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Exploring the Impact of a 7-Week Heart Rate Variability Biofeedback Protocol on Skin Severity, Quality of Life, and Mental Health in a Proof-of-Concept Pre–Post Trial of Individuals with Psoriasis
Background: Psoriasis often coexists with psychiatric disorders and decreased quality of life (QoL), with treatments commonly overlooking the psychological impact of the disease. Heart rate variability biofeedback (HRVB) may offer a mind–body solution by providing real-time feedback on autonomic functions, teaching individuals to manage stress via controlled breathing. Objective: To examine the impact of a 7-week HRVB protocol on skin severity (SS), QoL, and mental health (MH) in individuals with psoriasis and determine the sustainability of any outcomes post-intervention. Methods: A single-arm, proof-of-concept pre–post trial was conducted at Bastyr University Clinic in San Diego, CA. Five individuals were recruited, screened, and underwent a 7-week HRVB protocol. Assessments included SS through the Psoriasis Area and Severity Index (PASI-P and PASI-C), QoL via the Cardiff Dermatology Life Quality Index (DLQI), and MH using the Generalized Anxiety Disorder-7 (GAD-7) and Patient Health Questionnaire-9 (PHQ-9). Data collection points were baseline, post-protocol, and 1-month follow-up. Results: Notable improvements were observed between baseline and post-protocol for PASI-P, DLQI, and GAD-7. A significant change remained for GAD-7 between baseline and follow-up. No major differences were identified for PASI-C and PHQ-9 across any timeframe, and other scales remained consistent between post-protocol and follow-up. Conclusion: HRVB showed promise in enhancing perceived SS, QoL, and anxiety over 7 weeks. Further studies should expand participant numbers and diversify initial scores, comparing HRVB with a control group. Trial registration: ClinicalTrials.gov NCT05506644, retrospectively registered on 16 August 2022.
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