Clinical and cost-effectiveness of individualised exercises and foot orthoses in the treatment of plantar heel pain: protocol for the TREADON randomised multi-arm multi-stage adaptive trial.

NIHR open research Pub Date : 2025-05-06 eCollection Date: 2025-01-01 DOI:10.3310/nihropenres.13930.1
Martin J Thomas, Gemma Hughes, Kendra Cooke, Stephanie Butler-Walley, Emma Marshall, Laura Bowyer, Simon Wathall, Jo Smith, Sarah A Lawton, June Brammar, Thomas Burnett, Chris Drake, Nadine E Foster, Gordon J Hendry, Melaine A Holden, Thomas Jaki, Royes Joseph, Anne-Maree Keenan, Jesse Kigozi, Martyn Lewis, Christian D Mallen, Hylton B Menz, Pavel Mozgunov, Edward Roddy
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Abstract

Background: Plantar heel pain (PHP) is the most common soft tissue foot condition and impairs mobility, physical function, ability to work, and quality of life. Systematic reviews highlight a need for high-quality randomised controlled trials (RCTs) of exercises and orthoses for PHP.

Objectives: To determine the clinical and cost-effectiveness of individualised exercises and/or prefabricated foot orthoses plus self-management advice (SMA) compared to SMA alone in adults with PHP.

Methods: A multi-centre four-arm two-stage adaptive parallel-group RCT with internal pilot. Up to 696 participants aged ≥18 years with PHP will be identified from general practice, physiotherapy/podiatry referrals and self-referral, and randomised 1:1:1:1 to: (1) SMA (control), (2) SMA plus individualised exercises, (3) SMA plus prefabricated foot orthoses, or (4) SMA plus individualised exercises and prefabricated foot orthoses. Outcomes will be collected by SMS text-message (weekly during weeks 1-12, monthly during months 4-12) and questionnaires at 12 weeks and 6 and 12 months. The primary outcome is change in PHP intensity (0-10 numeric rating scale) between baseline and the average over 6-12 weeks. Interim analysis when 348 participants have completed the primary outcome assessment will inform adaptation, where interventions may be dropped or the trial stopped early (for efficacy or futility). The main between-group comparison for the primary outcome will be undertaken using linear mixed modelling. Secondary outcomes will examine i) short-term pain trajectories over weeks 1-12, ii) pain at 6 and 12 months, and monthly from 3-12 months, iii) first step pain, physical function, global rating of change, pain self-efficacy, illness perceptions, ability to work, and treatment satisfaction at 12 weeks, 6 and 12 months, iv) cost-effectiveness. Patient and public partner involvement is embedded throughout.

Discussion: The TREADON multi-arm multi-stage RCT will provide new evidence on the clinical and cost-effectiveness of individualised exercises and prefabricated foot orthoses for people with PHP.

Trial registration: ISRCTN 12418153. Registration date 06 December 2022 https://doi.org/10.1186/ISRCTN12418153.

个体化锻炼和足部矫形器治疗足底跟痛的临床和成本效益:TREADON随机多臂多阶段适应性试验方案
背景:足底后跟痛(PHP)是最常见的软组织足部疾病,它会损害活动能力、身体功能、工作能力和生活质量。系统评价强调需要高质量的随机对照试验(rct)的锻炼和矫形器的PHP。目的:确定个体化锻炼和/或预制足部矫形器加自我管理建议(SMA)与单独SMA在成人PHP患者中的临床和成本效益。方法:采用多中心四臂两期自适应平行组随机对照试验。将从全科医生、物理治疗/足部转诊和自我转诊中确定696名年龄≥18岁的PHP患者,并按1:1:1:1随机分为:(1)SMA(对照)、(2)SMA加个性化锻炼、(3)SMA加预制足部矫形器、或(4)SMA加个性化锻炼和预制足部矫形器。结果将通过短信收集(1-12周每周,4-12月每月),并在12周、6和12个月时进行问卷调查。主要结果是6-12周内基线和平均值之间PHP强度(0-10数值评定量表)的变化。当348名参与者完成了主要结果评估时,中期分析将为适应提供信息,在这种情况下,干预措施可能会被取消,或者试验可能会提前停止(为了有效或无效)。主要结果的主要组间比较将使用线性混合模型进行。次要结果将检查i) 1-12周的短期疼痛轨迹,ii) 6和12个月的疼痛,以及3-12个月的月度疼痛,iii)第一步疼痛,身体功能,整体变化评分,疼痛自我效能,疾病感知,工作能力,12周,6和12个月的治疗满意度,iv)成本效益。患者和公共合作伙伴的参与贯穿始终。讨论:TREADON多臂多阶段随机对照试验将为PHP患者个性化锻炼和预制足部矫形器的临床和成本效益提供新的证据。试验注册:ISRCTN 12418153。注册日期2022年12月6日https://doi.org/10.1186/ISRCTN12418153。
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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