有氧运动项目对截瘫患者神经性疼痛和生活质量的影响:随机对照试验研究方案。

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-09-02 DOI:10.1186/s13063-024-08430-0
Ankush Gera, Shefali Walia, Stuti Khanna, Garima Wadhwa
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引用次数: 0

摘要

背景:脊髓损伤(SCI)患者通常会遭受神经病理性疼痛的折磨,这种疼痛通常会导致残疾,并对患者的功能、参与和生活质量(QoL)产生负面影响。药物治疗在减轻神经病理性疼痛方面缺乏疗效,因此有必要研究药物治疗的替代方法。各种有氧运动的临床前证据显示对神经病理性疼痛有积极作用,但调查其在 SCI 患者中效果的科学研究却很有限:本研究是一项双盲、平行、两组、随机对照试验,采用干预性研究设计,旨在评估有氧运动项目对慢性截瘫患者神经性疼痛和生活质量(QoL)的影响。根据纳入标准,将从一家超级专科医院的康复科招募 30 名神经损伤程度为 T2 至 L2 的慢性截瘫患者。按照 1:1 的分配比例,参与者将被随机分配到两组中的一组。干预组将根据峰值心率使用手臂测力计进行高强度间歇训练(HIIT)有氧运动,对照组则进行徒手手臂有氧运动。两组的干预均为 30 分钟,每周四次,持续 6 周:国际脊髓损伤疼痛基本数据集 3.0 版将用于诊断和评估神经性疼痛及其对日常活动、情绪和睡眠的干扰。国际脊髓协会 QoL 基本数据集将用于评估 QoL,6 分钟推举测试距离将用于评估峰值心率和有氧运动能力:讨论:有氧运动项目的有效性将根据干预中期 3 周后和干预后 6 周后神经病理性疼痛评分及其对日常活动、情绪、睡眠、QoL 和有氧运动能力的干扰的变化进行评估。该试验将为有氧运动项目在改善慢性截瘫患者神经性疼痛和生活质量方面的有效性提供新的知识:试验注册:印度临床试验注册中心 CTRI/2023/08/056257。注册日期:2023 年 8 月 8 日。
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Effect of aerobic exercise program on neuropathic pain and quality of life in person with paraplegia: study protocol for a randomized controlled trial.

Background: Individuals with spinal cord injury (SCI) often suffer from neuropathic pain which is often disabling and negatively affects function, participation, and quality of life (QoL). Pharmacological treatments lack efficacy in neuropathic pain reduction hence studying alternatives to drug treatment is necessary. Preclinical evidence of various aerobic exercises has shown positive effects on neuropathic pain but scientific studies investigating its effect in the SCI human population are limited.

Methodology: This study is a double-blind, parallel, two-group, randomized controlled trial with an interventional study design that aims to evaluate the effectiveness of aerobic exercise program on neuropathic pain and quality of life (QoL) in individuals with chronic paraplegia. Thirty individuals with chronic paraplegia with the neurological level of injury from T2 to L2 will be recruited from the rehabilitation department at a super specialty hospital based on the inclusion criteria. Using a 1:1 allocation ratio, the participants will be randomly assigned to one of the two groups. The intervention group will perform high-intensity interval training (HIIT) aerobic exercise using an arm ergometer based on their peak heart rate, and the control group will perform free-hand arm aerobic exercise. In both groups, the intervention will be delivered as 30-min sessions, four times a week for 6 weeks.

Outcome measures: International Spinal Cord Injury Pain Basic Data Set Version 3.0 will be used for diagnosing and assessing neuropathic pain and its interference with day-to-day activities, mood, and sleep. The International Spinal Cord Society (ISCoS) QoL basic data set will be used to assess QoL, and 6-min push test distance will be used to assess peak heart rate and aerobic capacity.

Discussion: The effectiveness of the aerobic exercise program will be assessed based on the changes in neuropathic pain score and its interference with day-to-day activities, mood, sleep, QoL, and aerobic capacity after 3 weeks mid-intervention and after 6 weeks post-intervention. The trial will provide new knowledge about the effectiveness of the aerobic exercise program in improving neuropathic pain and QoL in individuals with chronic paraplegia.

Trial registration: Clinical Trials Registry-India CTRI/2023/08/056257. Registered on 8 August 2023.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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