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临床试验/NCT06356181
NCT06356181已完成不适用

High-Intensity Functional Training Adaptations With and Without Maximus Ventilatory Training Device

University of South Carolina1 个研究点 分布在 1 个国家目标入组 32 人开始时间: 2024年3月18日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
32
试验地点
1
主要终点
Changes in spirometry

研究概览

简要总结

This project aims to assess the effectiveness of using a Respiratory Muscle Training (RMT) device during high-intensity functional training (HIFT) to improve fitness and ventilatory parameters. Primary outcome measures include aerobic, anaerobic, and HIFT measures. Secondary measures include sleep, affect, and mood state questionnaires. Participants will be randomized into one of two groups: with the RMT device and without the RMT device.

详细描述

This study assesses the impact of a ventilatory training device, similar to a sports mouth guard worn during exercise, on various performance outcomes. The main questions it aims to answer are:

  • Does the device improve fitness parameters: high-intensity functional training, anaerobic capacity, anaerobic peak and mean power output, maximal oxygen uptake, ventilatory threshold, and blood lactate responses to training?
  • Does the device improve spirometry measures?

Researchers will compare 6 weeks of training with the ventilatory training device to those without the training device.

Participants will:

  • Take part in a total of 8 weeks of study-related activity.
  • Complete six total one- to two-hour pre- and post-testing sessions, which include a maximal oxygen uptake test, high-intensity functional training, body composition, spirometry, anaerobic power and capacity testing.
  • Complete six weeks of 45-minute high-intensity functional training, three days per week.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
None

入排标准

年龄范围
18 Years 至 35 Years(Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Males and females between the ages of 18 and 35 (inclusive) who participate in at least 150 minutes per week of physical activity.
  • •Have not participated in HIFT training in the last 6 months.
  • •Provided written and dated informed consent to participate in the study.
  • •In good health as determined by medical history and is cleared for exercise.
  • •Participant will be asked about dietary supplementation use within the past 6 months.
  • •If participant began taking a supplement within the past month, subject will be asked to discontinue supplement use followed by a 2-week washout prior to participation.
  • •In all other cases, we will request that participant maintain supplement use.

排除标准

  • •Any musculoskeletal injuries that would prevent exercising.
  • •Any metabolic disorder including known electrolyte abnormalities, diabetes, uncontrolled thyroid disease, adrenal disease or hypogonadism.
  • •Any inborn error of metabolism.
  • •History of hepatorenal, musculoskeletal, autoimmune, or neurologic disease.
  • •Participants with a personal history of heart disease, high blood pressure (systolic >140 mm Hg & diastolic >90 mm Hg),
  • •Participants who are pregnant, planning to become pregnant, or lactating.

研究组 & 干预措施

Experimental

Experimental

Participants in this group will undergo 6 weeks of high-intensity functional training using the respiratory muscle training device.

干预措施: Respiratory Maximus Training Device (Device)

Control

Active Comparator

Participants in this group will undergo 6 weeks of high-intensity functional training without using the respiratory muscle training device.

干预措施: No Respiratory Training Device (Device)

结局指标

主要结局

Changes in spirometry

时间窗: Baseline and Week 8

Spirometry measures of forced vital capacity (FVC) (L), forced expiratory volume at one second (FEV1) (L), and the ratio of FEV1/FVC %

Changes in aerobic capacity

时间窗: Baseline and Week 8

Assessed via a cycle-ergometer based maximal graded exercise test with indirect calorimetry.

Changes in countermovement jump

时间窗: Baseline and Week 8

Assessed via force plates

Changes in peak power

时间窗: Baseline and Week 8

Assessed via a cycle-ergometer based maximal graded exercise test

Changes in anaerobic capacity

时间窗: Baseline and Week 8

Assessed via 30-second Wingate test.

Changes in high-intensity functional training test

时间窗: Baseline and Week 8

Assessed via a high-intensity functional training circuit composed of rows, pushups, and squats

Changes in ventilatory threshold

时间窗: Baseline and Week 8

Assessed via a cycle-ergometer based maximal graded exercise test with indirect calorimetry.

Changes in heart rate at ventilatory threshold

时间窗: Baseline and Week 8

Assessed via a cycle-ergometer based maximal graded exercise test with indirect calorimetry.

次要结局

  • Changes in body composition(Baseline and Week 8)
  • Changes in positive mood and emotion(Baseline and Weeks 3, 5, and 7)
  • Changes in total mood disturbances(Baseline and Weeks 3, 5, and 7)
  • Changes in sleep quality(Baseline and Weeks 3, 5, and 7)
  • Change in blood lactate responses(Weeks 3, 5, and 7)
  • Changes in negative mood and emotion(Baseline and Weeks 3, 5, and 7.)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Shawn M. Arent

Professor and Chair of Exercise Science Department

University of South Carolina

研究点 (1)

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