阻力运动时的努力程度对糖尿病前期或 2 型糖尿病患者血糖控制的影响:交叉随机对照试验方案。

IF 1.4 Q3 HEALTH CARE SCIENCES & SERVICES
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引用次数: 0

摘要

背景:2 型糖尿病(T2D)的前身是糖尿病前期,这些病症给患者和社会带来了沉重负担。这些病症与血糖控制不佳密切相关,而阻力运动可改善血糖控制。有人认为,阻力运动应在高度努力的情况下进行,以改善葡萄糖代谢,但这与消极的心理反应有关,可能导致长期坚持运动的人数减少:本研究旨在调查阻力运动时的用力程度对糖尿病前期或 T2D 患者血糖控制和心理反应的影响:本研究将采用交叉、三臂、随机对照试验。共有 15 名糖尿病前期或 T2D 患者将彻底熟悉 7 种阻力练习;之后,他们将进行 3 次随机实验,每次持续约 48 小时,中间至少有 4 天的冲洗期。在其中的两次实验中,将在监督下进行阻力训练,但每次训练的强度不同(大强度与小强度),举起的总重量和持续时间也相同。为此,将通过改变每组运动的次数、每组运动的重复次数以及每组运动和运动之间的休息间隔来控制接近失败的程度。参与者还将完成静坐(对照组)训练,不做任何运动。针对每个训练环节,将对参与者的心理反应进行评估(消耗、情绪、乐趣、自我效能感和不适感)。在每个实验环节的大约 48 小时内,每 5 分钟将通过连续血糖监测设备对血糖控制情况进行评估。食物和饮料将由注册营养师单独开具处方并提供给参与者,以控制能量摄入和饮食成分的混杂效应。运动量将通过加速度计进行评估。随机化将采用不透明、按顺序编号的信封技术进行。参与者和研究人员将对连续血糖监测和加速度测量数据进行盲测,数据将由盲测统计员进行分析:这项研究已获得资助,数据收集工作预计将于 2024 年 6 月至 2025 年 5 月间进行。最终稿件将于 2025 年 8 月提交:本项目的结果可能会鼓励糖尿病前期和 T2D 患者参与阻力运动,同时让运动专家更好地了解如何将阻力运动最好地融入客户或患者的日常活动中:试验注册:ClinicalTrials.gov NCT06208189;https://clinicaltrials.gov/study/NCT06208189.International 注册报告标识符 (irrid):PRR1-10.2196/63598。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Effect of Effort During a Resistance Exercise Session on Glycemic Control in Individuals Living With Prediabetes or Type 2 Diabetes: Protocol for a Crossover Randomized Controlled Trial.

Background: Type 2 diabetes (T2D) is preceded by prediabetes, and these conditions place a great burden on patients and society. These conditions are significantly associated with poor glycemic control, which is improved by resistance exercise. It has been suggested that resistance exercise should be performed with a high degree of effort to improve glucose metabolism, but this is associated with negative psychological responses that might lead to lower long-term adherence.

Objective: This study aimed to investigate the effect of the degree of effort during a resistance exercise session on glycemic control and psychological responses in individuals living with prediabetes or T2D.

Methods: This study will be a crossover, 3-arm, randomized controlled trial. A total of 15 participants living with prediabetes or T2D will be thoroughly familiarized with 7 resistance exercises; afterward, they will perform 3 randomized experimental sessions, each lasting approximately 48 hours each, separated by at least 4 washout days. In 2 of these sessions, supervised resistance exercise will be performed, but the sessions will differ in the degree of effort in each set (high vs low) and will be equalized in terms of total weight lifted and session duration. For this, proximity to failure will be manipulated by changing the number of sets per exercise, the number of repetitions per set, and the resting interval between sets and exercises. Participants will also complete a sedentary (control) session, where they will not perform any exercise. In response to each session, psychological responses will be assessed (exertion, affect, enjoyment, self-efficacy, and discomfort). Glycemic control will be assessed by a continuous glucose monitoring device every 5 minutes, throughout the approximately 48 hours of each experimental session. Food and drink will be individually prescribed by a registered dietitian nutritionist and provided to participants, in order to control for the confounding effect of energy intake and diet composition. Physical activity levels will be assessed by accelerometry. Randomization will be done using the opaque, sequentially numbered envelopes technique. Participants and researchers will be blinded for continuous glucose monitoring and accelerometry data, and data will be analyzed by a blinded statistician.

Results: This study has been funded, and data collection is expected to take place between June 2024 and May 2025. Final manuscript submission should happen by August 2025.

Conclusions: The results of this project might encourage individuals living with prediabetes and T2D to engage in resistance exercise while better informing exercise specialists on how to best incorporate resistance exercise in their client's or patient's routine.

Trial registration: ClinicalTrials.gov NCT06208189; https://clinicaltrials.gov/study/NCT06208189.

International registered report identifier (irrid): PRR1-10.2196/63598.

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来源期刊
CiteScore
2.40
自引率
5.90%
发文量
414
审稿时长
12 weeks
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