Smith Samuel G, Ellison Rachel, Hall Louise, Clark Jane, Hartley Suzanne, Mason Ellen, Metherell Jamie, Olivier Catherine, Napp Vicky, Naik Jay, Buckley Sarah, Hirst Charlotte, Hartup Sue, Neal Richard D, Velikova Galina, Farrin Amanda, Collinson Michelle, Graham Christopher D
Leeds Institute of Health Science, University of Leeds, Leeds, LS2 9JT, UK.
Clinical Trials Research Unit, Leeds Institute of Clinical Trials Research, University of Leeds, Leeds, LS2 9JT, UK.
Pilot Feasibility Stud. 2022 Feb 8;8(1):33. doi: 10.1186/s40814-022-00985-6.
Adherence to adjuvant endocrine therapy is affected by medication side-effects and associated distress. Previous interventions focused on educating women to enhance adherence have proved minimally effective. We co-designed an Acceptance and Commitment Therapy (ACT) intervention to enhance medication decision-making and quality of life by targeting a broader range of factors, including side-effect management and psychological flexibility. This study aims to establish key trial parameters, assess the acceptability of the intervention and the extent to which it can be delivered with fidelity, and to demonstrate "proof of principle" regarding its efficacy on primary and process outcomes.
The ACTION intervention includes an individual 1:1 ACT session followed by three group sessions involving 8-10 women and two practitioner psychologists. Participants are also provided with access to a website containing evidence-based methods for self-managing side-effects. The ACT sessions were adapted during the COVID-19 pandemic to be remotely delivered via video conferencing software. To evaluate the feasibility and acceptability of this intervention, a multi-site, exploratory, two-arm, individually randomised external pilot trial with a nested qualitative study will be undertaken. Eighty women with early stage breast cancer prescribed adjuvant endocrine therapy will be randomised (1:1) to receive treatment as usual or treatment as usual plus the ACTION intervention. The planned future primary outcome is medication adherence assessed by the ASK-12 measure. Progression to a phase III RCT will be based on criteria related to recruitment and follow-up rates, acceptability to patients, competency and fidelity of delivery, and proof of principle for change in medication adherence.
This external pilot trial will be used to ascertain the feasibility of undertaking a future phase III RCT to definitively evaluate an ACT-based intervention to support medication taking behaviour and quality of life in women with early stage breast cancer on adjuvant endocrine therapy.
ISRCTN: 12027752. Registered 24 December 2020, https://doi.org/10.1186/ISRCTN12027752.
辅助内分泌治疗的依从性受药物副作用及相关困扰的影响。以往专注于教育女性以提高依从性的干预措施效果甚微。我们共同设计了一种接受与承诺疗法(ACT)干预措施,通过针对更广泛的因素,包括副作用管理和心理灵活性,来提高用药决策和生活质量。本研究旨在确定关键试验参数,评估干预措施的可接受性及其能够忠实实施的程度,并证明其对主要结局和过程结局有效性的“原理证明”。
ACT干预包括一次一对一的个体ACT治疗,随后是三次小组治疗,每次有8 - 10名女性和两名执业心理学家参与。还为参与者提供访问一个包含基于证据的副作用自我管理方法的网站。在新冠疫情期间,ACT治疗通过视频会议软件改为远程提供。为评估该干预措施的可行性和可接受性,将开展一项多中心、探索性、双臂、个体随机的外部预试验,并嵌套定性研究。80名接受辅助内分泌治疗的早期乳腺癌女性将被随机分组(1:1),分别接受常规治疗或常规治疗加ACT干预。计划中的未来主要结局是通过ASK - 12量表评估的用药依从性。向III期随机对照试验的推进将基于与招募和随访率、患者可接受性、实施的能力和忠实性以及用药依从性变化的原理证明相关的标准。
这项外部预试验将用于确定开展未来III期随机对照试验的可行性,以最终评估基于ACT的干预措施对接受辅助内分泌治疗的早期乳腺癌女性服药行为和生活质量的支持作用。
ISRCTN:12027752。于2020年12月24日注册,https://doi.org/10.1186/ISRCTN12027752 。