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Smartphone App Using Mindfulness Meditation for Women With Chronic Pelvic Pain (MEMPHIS): Protocol for a Randomized Feasibility Trial

机译:智能手机应用程序使用正念冥想治疗慢性盆腔痛(MEMPHIS)妇女:一项随机可行性试验方案

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Background Female chronic pelvic pain (CPP) is defined as intermittent or constant pelvic or lower abdominal pain occurring in a woman for at least 6 months. Up to a quarter of women are estimated to be affected by CPP worldwide and it is responsible for one fifth of specialist gynecological referrals in the United Kingdom. Psychological interventions are commonly utilized. As waiting times and funding capacity impede access to face-to-face consultations, supported self-management (SSM) has emerged as a viable alternative. Mindfulness meditation is a potentially valuable SSM tool, and in the era of mobile technology, this can be delivered to the individual user via a smartphone app. Objective To assess the feasibility of conducting a trial of a mindfulness meditation intervention delivered by a mobile phone app for patients with CPP. The main feasibility objectives were to assess patient recruitment and app adherence, to obtain information to be used in the sample size estimate of a future trial, and to receive feedback on usability of the app. Methods Mindfulness Meditation for Women With Chronic Pelvic Pain (MEMPHIS) is a three-arm feasibility trial, that took place in two hospitals in the United Kingdom. Eligible participants were randomized in a 1:1:1 ratio to one of three treatment arms: (1) the intervention arm, consisting of a guided, spoken mindfulness meditation app; (2) an active control arm, consisting of a progressive muscle relaxation app; and (3) usual care (no app). Participants were followed-up for 6 months. Key feasibility outcomes included the time taken to recruit all patients for the study, adherence, and estimates to be used in the sample size calculation for a subsequent full-scale trial. Upon completion of the feasibility trial we will conduct focus groups to explore app usability and reasons for noncompliance. Results Recruitment for MEMPHIS took place between May 2016 and September 2016. The study was closed March 2017 and the report was submitted to the NIHR on October 26, 2017. Conclusions This feasibility trial will inform the design of a large multicentered trial to assess the clinical effectiveness of mindfulness meditation delivered via a smartphone app for the treatment of CPP. Trial Registration ClinicalTrials.gov: {"type":"clinical-trial","attrs":{"text":"NCT02721108","term_id":"NCT02721108"}} NCT02721108 ; https://clinicaltrials.gov/ct2/show/ {"type":"clinical-trial","attrs":{"text":"NCT02721108","term_id":"NCT02721108"}} NCT02721108 (Archived by WebCite at http://www.webcitation.org/6wLMAkuaU); BioMed Central: ISRCTN10925965; https://www.isrctn.com/ISRCTN10925965 (Archived by WebCite at http://www.webcitation.org/6wLMVLuys).
机译:背景技术女性慢性盆腔痛(CPP)定义为女性至少持续6个月的间歇性或持续性盆腔痛或下腹部痛。据估计,全世界有四分之一的妇女受到CPP的影响,并且该病占英国专科妇科转诊的五分之一。通常采用心理干预。由于等待时间和筹资能力阻碍了面对面磋商,因此,支持的自我管理(SSM)已成为一种可行的选择。正念冥想是一种潜在有价值的SSM工具,在移动技术时代,可以通过智能手机应用程序将其传递给个人用户。目的评估通过手机应用程序对CPP患者进行正念冥想干预试验的可行性。主要的可行性目标是评估患者的招募和应用程序的依从性,获取要用于未来试验的样本量估计的信息,并接收有关应用程序可用性的反馈。方法慢性盆腔痛女性正念冥想(MEMPHIS)是一项三臂可行性试验,在英国的两家医院进行。符合条件的参与者以1:1:1的比例随机分配到三个治疗组之一:(1)干预组,包括一个指导性的口头正念冥想应用程序; (2)主动控制臂,由渐进式肌肉放松应用程序组成; (3)日常护理(无应用程序)。参加者随访6个月。关键的可行性结果包括招募所有患者进行研究所需的时间,依从性以及用于随后的全面试验的样本量计算所用的估计值。可行性试验完成后,我们将进行焦点小组讨论,以探讨应用程序的可用性和不合规的原因。结果MEMPHIS的征募于2016年5月至2016年9月之间进行。研究于2017年3月结束,报告于2017年10月26日提交给NIHR。结论该可行性试验将为大型多中心试验的设计提供依据,以评估临床通过智能手机应用程序提供的正念冥想治疗CPP的有效性。试用注册ClinicalTrials.gov:{“ type”:“ clinical-trial”,“ attrs”:{“ text”:“ NCT02721108”,“ term_id”:“ NCT02721108”}} NCT02721108; https://clinicaltrials.gov/ct2/show/ {“ type”:“ clinical-trial”,“ attrs”:{“ text”:“ NCT02721108”,“ term_id”:“ NCT02721108”}} NCT02721108(由WebCite存档在http://www.webcitation.org/6wLMAkuaU); BioMed Central:ISRCTN10925965; https://www.isrctn.com/ISRCTN10925965(由WebCite存档,网址为http://www.webcitation.org/6wLMVLuys)。

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