Virtual Intervention for Vertebral frActures (VIVA): protocol for a feasibility study of a multicentre randomized controlled trial.

IF 1.5 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Ada Sevinc, Alexandra Papaioannou, Suzanne N Morin, Jennifer A Watt, Raheem B Kherani, Sheila Brien, Larry Funnell, Lehana Thabane, Lauren A Beaupre, Jenna C Gibbs, Heather Keller, Caitlin McArthur, Matteo Ponzano, Sonia Singh, Sharon Straus, Jenny Thain, Zachary J Weston, Timothy H Wideman, Christopher D Witiw, Lora Giangregorio
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引用次数: 0

Abstract

Background: Vertebral fractures due to osteoporosis cause significant pain and disability. There is guidance available on the management of osteoporotic vertebral fractures, informed by systematic reviews and a consensus process. However, few studies examine whether implementing pragmatic and patient-oriented rehabilitation interventions can improve outcomes for individuals with a vertebral fracture.

Methods: The purpose of the study is to investigate the feasibility of a multicentre randomized controlled trial of an 8-week virtual rehabilitation intervention for people with an osteoporotic vertebral fracture in Ontario, British Columbia, and Quebec. The design is a multicentre randomized controlled trial with two parallel groups randomized in a 1:1 ratio, stratified by centre to immediate or delayed (10 weeks after randomization) receipt of the Virtual Intervention for Vertebral frActures (VIVA). Four centres will each recruit eight individuals (total n = 32) over the age of 50 who have had at least one vertebral fracture in the past 2 years confirmed by a radiology report. VIVA involves once weekly virtual rehabilitation sessions delivered over 8 weeks by an exercise professional, covering four areas: pain management, safe movement, exercise, and nutrition. Exercise professional provides resources and prescribes exercise therapy for participants to implement outside of the scheduled sessions. The primary feasibility outcomes are recruitment, retention, and adherence, and criteria for success are as follows: (a) recruiting eight people per site in 5 months, (b) 80% of participants completing the trial, and (c) 75% adherence to the virtual rehabilitation sessions. The secondary outcomes include costs relative to benefit, effects on health-related outcomes (e.g. 30-s chair stand, Brief Pain Inventory, Quality of Life Questionnaire of the European Foundation for Osteoporosis-41, SCREEN-14), and outcomes related to implementation (e.g. participant and provider experience using semi-structured interviews, fidelity, number of screened and enrolled participants by referral source, fracture verification process). Descriptive analyses (e.g. mean, count, percentage) will be performed for primary feasibility outcomes and secondary outcomes.

Discussion: The results will establish the feasibility of a future trial investigating the effectiveness of the VIVA intervention in people with an osteoporotic vertebral fracture.

Trial registration: The trial was registered in ClinicalTrials.gov on October 21, 2024 (NCT06650410), https://clinicaltrials.gov/study/NCT06650410 .

椎体骨折虚拟干预(VIVA):一项多中心随机对照试验的可行性研究方案。
背景:骨质疏松引起的椎体骨折会引起明显的疼痛和残疾。有关于骨质疏松性椎体骨折管理的指导,通过系统的回顾和共识的过程。然而,很少有研究调查实施实用的和以患者为导向的康复干预是否能改善椎体骨折患者的预后。方法:本研究的目的是探讨在安大略省、不列颠哥伦比亚省和魁北克省对骨质疏松性椎体骨折患者进行8周虚拟康复干预的多中心随机对照试验的可行性。该设计是一项多中心随机对照试验,两个平行组按1:1的比例随机分组,按中心分层,立即或延迟(随机化后10周)接受椎体骨折虚拟干预(VIVA)。4个中心将分别招募8名年龄在50岁以上且在过去2年内至少有过一次椎体骨折且经放射学报告证实的患者(共32人)。VIVA包括每周一次的虚拟康复课程,由运动专家提供,为期8周,涵盖四个方面:疼痛管理,安全运动,运动和营养。运动专业人士为参与者提供资源和规定的运动疗法,以实施计划之外的会议。主要的可行性结果是招募、保留和坚持,成功的标准如下:(a)每个站点在5个月内招募8人,(b) 80%的参与者完成试验,(c) 75%的参与者坚持虚拟康复课程。次要结局包括与获益相关的成本、对健康相关结局的影响(例如30-s座椅支架、简短疼痛量表、欧洲骨质疏松基金会生活质量问卷-41、SCREEN-14),以及与实施相关的结局(例如使用半结构化访谈的参与者和提供者经验、保真度、通过转诊来源筛选和登记的参与者人数、骨折验证过程)。将对主要可行性结果和次要可行性结果进行描述性分析(例如平均值、计数、百分比)。讨论:该结果将为未来研究VIVA干预对骨质疏松性椎体骨折患者的有效性奠定基础。试验注册:该试验已于2024年10月21日在ClinicalTrials.gov (NCT06650410)注册,网址为https://clinicaltrials.gov/study/NCT06650410。
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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来源期刊
Pilot and Feasibility Studies
Pilot and Feasibility Studies Medicine-Medicine (miscellaneous)
CiteScore
2.70
自引率
5.90%
发文量
241
审稿时长
9 weeks
期刊介绍: Pilot and Feasibility Studies encompasses all aspects of the design, conduct and reporting of pilot and feasibility studies in biomedicine. The journal publishes research articles that are intended to directly influence future clinical trials or large scale observational studies, as well as protocols, commentaries and methodology articles. The journal also ensures that the results of all well-conducted, peer-reviewed, pilot and feasibility studies are published, regardless of outcome or significance of findings. Pilot and feasibility studies are increasingly conducted prior to a full randomized controlled trial. However, these studies often lack clear objectives, many remain unpublished, and there is confusion over the meanings of the words “pilot” and “feasibility”. Pilot and Feasibility Studies provides a forum for discussion around this key aspect of the scientific process, and seeks to ensure that these studies are published, so as to complete the publication thread for clinical research.
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