BPSDiary study protocol: a multi-center randomized controlled trial to compare the efficacy of a BPSD diary vs. standard care in reducing caregiver's burden

F. Pozzi, Luisa Calì, F. D’Antonio, Arianna Ida Altomare, Micaela Sepe Monti, Massimiliano Panigutti, Adolfo Di Crosta, R. Palumbo, L. Bonanni, Valentina Carlucci, Cinzia Bussè, Annachiara Cagning, D. Urso, D. Vilella, Giancarlo Logroscino, M. Alberoni, Angelo Bellinvia, Elisabetta Farina, F. de Rino, Armando Gavazzi, Marta Zuffi, Giuseppe Bruno, Valentina Bessi, M. Cotta Ramusino, G. Perini, Alfredo Costa, C. Ferrarese, I. Appollonio, L. Tremolizzo
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Abstract

Behavioral and Psychological Symptoms of Dementia (BPSD) are a heterogeneous set of psychological and behavioral abnormalities seen in persons with dementia (PwD), significantly impacting their quality of life and that of their caregivers. Current assessment tools, such as the Neuropsychiatric Inventory (NPI), are limited by recall bias and lack of direct observation. This study aims to overcome this limitation by making caregiver reports more objective through the use of a novel instrument, referred to as the BPSDiary. This randomized controlled trial will involve 300 caregiver-PwD dyads. The objective is to evaluate whether the use of the BPSDiary could significantly reduce caregiver burden, assessed using the Zarit Burden Interview (ZBI), compared to usual care. The study will include adult PwD, caregivers living with or close to the patient, and BPSD related to the HIDA (hyperactivity, impulsivity, irritability, disinhibition, aggression, agitation) domain. Caregivers randomized to the intervention arm will use the BPSDiary to record specific BPSD, including insomnia, agitation/anxiety, aggression, purposeless motor behavior, and delusions/hallucinations, registering time of onset, severity, and potential triggers. The primary outcome will be the change in ZBI scores at 3 months, with secondary outcomes including changes in NPI scores, olanzapine equivalents, NPI-distress scores related to specific BPSD domains, and caregiver and physician satisfaction. The study will be conducted in 9 Italian centers, representing diverse geographic and sociocultural contexts. While potential limitations include the relatively short observation period and the focus on specific BPSD disturbances, the BPSDiary could provide physicians with objective data to tailor appropriate non-pharmacological and pharmacological interventions. Additionally, it may empower caregivers by encouraging reflection on BPSD triggers, with the potential to improve the quality of life for both PwD and their caregivers.NCT05977855.
BPSDiary 研究方案:多中心随机对照试验,比较 BPSD 日记与标准护理在减轻护理人员负担方面的效果
痴呆症的行为和心理症状(BPSD)是痴呆症患者(PwD)的一系列心理和行为异常,严重影响了他们及其护理者的生活质量。目前的评估工具,如神经精神量表(NPI),受到回忆偏差和缺乏直接观察的限制。本研究旨在通过使用一种名为 "BPSDiary "的新型工具,使护理人员的报告更加客观,从而克服这一局限性。这项随机对照试验将涉及 300 个照护者-残疾人二人组。目的是评估与常规护理相比,使用 BPSDiary 是否能显著减轻护理者的负担(使用 Zarit 负担访谈 (ZBI) 进行评估)。研究对象包括成年残疾人、与患者同住或与患者关系密切的护理人员,以及与 HIDA(多动、冲动、易怒、抑制、攻击、激动)领域相关的 BPSD。随机加入干预组的护理人员将使用 BPSD 日记记录特定的 BPSD,包括失眠、激动/焦虑、攻击性、无目的运动行为和妄想/幻觉,并记录发病时间、严重程度和潜在诱因。主要结果是 3 个月后 ZBI 评分的变化,次要结果包括 NPI 评分、奥氮平当量、与特定 BPSD 领域相关的 NPI 压力评分以及护理人员和医生满意度的变化。该研究将在 9 个意大利中心进行,这些中心代表了不同的地理和社会文化背景。虽然潜在的局限性包括观察期相对较短和只关注特定的 BPSD 干扰,但 BPSD 日志可为医生提供客观数据,以定制适当的非药物和药物干预措施。此外,它还可以通过鼓励对 BPSD 诱因进行反思来增强护理人员的能力,从而有可能提高残疾人及其护理人员的生活质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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