一项多中心、随机、为期12个月的平行组可行性研究,旨在评估家庭导航加常规护理与常规护理相比在管理儿童肥胖症时对减少失访的可接受性和初步影响:一项研究方案。
A multi-center, randomized, 12-month, parallel-group, feasibility study to assess the acceptability and preliminary impact of family navigation plus usual care versus usual care on attrition in managing pediatric obesity: a study protocol.
作者信息
Ball Geoff D C, O'Neill Marcus G, Noor Rafat, Alberga Angela, Azar Rima, Buchholz Annick, Enright Michelle, Geller Josie, Ho Josephine, Holt Nicholas L, Lebel Tracy, Rosychuk Rhonda J, Tarride Jean-Eric, Zenlea Ian
机构信息
Department of Pediatrics, University of Alberta, 4-515 Edmonton Clinic Health Academy, 11405 87th Ave, Edmonton, AB, T6G 1C9, Canada.
Department of Health, Kinesiology, and Applied Physiology, Concordia University, Montreal, QC, Canada.
出版信息
Pilot Feasibility Stud. 2023 Jan 23;9(1):14. doi: 10.1186/s40814-023-01246-w.
BACKGROUND
Pediatric obesity management can be successful, but some families discontinue care prematurely (i.e., attrition), limiting treatment impact. Attrition is often a consequence of barriers and constraints that limit families' access to obesity management. Family Navigation (FN) can improve access, satisfaction with care, and treatment outcomes in diverse areas of healthcare. To help our team prepare for a future effectiveness trial, the objectives of our randomized feasibility study are to (i) explore children's and caregivers' acceptability of FN and (ii) examine attrition, measures of study rigor and conduct, and responses to FN + Usual Care vs Usual Care by collecting clinical, health services, and health economic data.
METHODS
In our 2.5-year study, 108 6-17-year-olds with obesity and their caregivers will be randomized (1:1) to FN + Usual Care or Usual Care after they enroll in obesity management clinics in Calgary and Mississauga, Canada. Our Stakeholder Steering Committee and research team will use Experience-Based Co-Design to design and refine our FN intervention to reduce families' barriers to care, maximizing the intervention dose families receive. FN will be delivered by a navigator at each site who will use logistical and relational strategies to enhance access to care, supplementing obesity management. Usual Care will be offered similarly at both clinics, adhering to expert guidelines. At enrollment, families will complete a multidisciplinary assessment, then meet regularly with a multidisciplinary team of clinicians for obesity management. Over 12 months, both FN and Usual Care will be delivered virtually and/or in-person, pandemic permitting. Data will be collected at 0, 3, 6, and 12 months post-baseline. We will explore child and caregiver perceptions of FN acceptability as well as evaluate attrition, recruitment, enrolment, randomization, and protocol integrity against pre-set success thresholds. Data on clinical, health services, and health economic outcomes will be collected using established protocols. Qualitative data analysis will apply thematic analysis; quantitative data analysis will be descriptive.
DISCUSSION
Our trial will assess the feasibility of FN to address attrition in managing pediatric obesity. Study data will inform a future effectiveness trial, which will be designed to test whether FN reduces attrition.
TRIAL REGISTRATION
This trial was registered prospectively at ClinicalTrials.gov (# NCT05403658 ; first posted: June 3, 2022).
背景
儿童肥胖管理可以取得成功,但一些家庭会过早中断治疗(即退出),从而限制了治疗效果。退出往往是限制家庭获得肥胖管理服务的障碍和制约因素导致的结果。家庭导航(FN)可以改善在不同医疗领域的服务可及性、护理满意度和治疗效果。为帮助我们的团队为未来的有效性试验做好准备,我们随机可行性研究的目标是:(i)探索儿童和照顾者对FN的接受度;(ii)通过收集临床、卫生服务和卫生经济数据,检查退出情况、研究严谨性和实施情况的衡量指标,以及FN+常规护理与常规护理的反应。
方法
在我们为期2.5年的研究中,108名6至17岁的肥胖儿童及其照顾者在加拿大卡尔加里和密西沙加的肥胖管理诊所登记后,将被随机(1:1)分配到FN+常规护理组或常规护理组。我们的利益相关者指导委员会和研究团队将使用基于经验的协同设计来设计和完善我们的FN干预措施,以减少家庭获得护理的障碍,使家庭接受的干预剂量最大化。FN将由每个地点的一名导航员提供,该导航员将使用后勤和关系策略来增加护理可及性,辅助肥胖管理。两家诊所将以类似方式提供常规护理,遵循专家指南。登记时,家庭将完成多学科评估,然后定期与多学科临床医生团队会面进行肥胖管理。在12个月内,在疫情允许的情况下,FN和常规护理将通过虚拟和/或面对面的方式提供。将在基线后0、3、6和12个月收集数据。我们将探索儿童和照顾者对FN可接受性的看法,并根据预先设定的成功阈值评估退出情况、招募、登记、随机化和方案完整性。将使用既定方案收集临床、卫生服务和卫生经济结果的数据。定性数据分析将采用主题分析;定量数据分析将采用描述性分析。
讨论
我们的试验将评估FN解决儿童肥胖管理中退出问题的可行性。研究数据将为未来的有效性试验提供信息,该试验将旨在测试FN是否能减少退出情况。
试验注册
本试验已在ClinicalTrials.gov上进行前瞻性注册(#NCT05403658;首次发布:2022年6月3日)。
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