跳至主要内容
临床试验/NCT06459674
NCT06459674已完成不适用

Mean ReSponse Time: Effects of Inspiratory Muscle Training in Postmenopausal Women (MRS)

Indiana University1 个研究点 分布在 1 个国家目标入组 28 人开始时间: 2024年4月12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
28
试验地点
1
主要终点
Duration

研究概览

简要总结

This study is being conducted by the Department of Kinesiology within the School of Public Health at Indiana University Bloomington. The purpose of this study is to better understand how inspiratory muscle strength training affects cardiovascular health and mood disturbance in postmenopausal women.

详细描述

Inspiratory muscle training (IMT) works by strengthening the respiratory muscles through resistive airflow breathing using a handheld device. The goal being to elicit an adaptive response akin to resistance exercise for locomotor muscles. Labored breathing due to respiratory muscle weakness can detract from physical performance with attendant consequences on independent living. This may trigger a maladaptive cycle that worsens physiological and psychosocial outcomes. IMT from 6-10 weeks has been shown to increase maximal inspiratory pressure, functional capacity, and perceived breathlessness across disease states. To inform an appropriately powered randomized controlled trial, the present work proposes a 2-arm single-blind, randomized pilot study to evaluate outcomes of interest.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Investigator)

盲法说明

All members of the research staff (i.e., those collecting data during experimental visits) will be blinded to the treatment group. The PI, who will not be part of data collection, will not be blinded.

入排标准

年龄范围
50 Years 至 75 Years(Adult, Older Adult)
性别
Female
接受健康志愿者
是

入选标准

  • •Postmenopausal women (self-report at least 6 years since last menstrual cycle)
  • •Aged 50-75 years (confirmed by birth date listed on participant's driver license at screening visit)
  • •English-speaking
  • •Body mass index between 25.0 to 39.9 kg/m2
  • •Able to ambulate without assistance
  • •Own or have access to a Bluetooth-capable phone or tablet (IOS version 12.0 or later or Android version 7.0 or later)

排除标准

  • •Unable to provide informed consent.
  • •Greater than stage II hypertension (i.e., >159/99 mm Hg)
  • •Current tobacco use (self-report)
  • •Habitually exercise training ≥ 2 days per week (self-report)
  • •Significant orthopedic limitations or other contraindications to strenuous exercise
  • •Live or work > 80 miles from Bloomington, Indiana
  • •Anticipated elective surgery during the study period.
  • •Surgery to the chest or abdomen in the last 6 months.
  • •Plan to move residence or travel out of the local area during the study period.
  • •History of heart attack or heart condition.
  • •Current use of prescription medications that affect heart rate or blood vessel dilation (e.g., systemic b-adrenergic blockers, calcium channel blockers, and hormone replacement therapy).
  • •Diagnosis of asthma or chronic pulmonary disease.
  • •Current respiratory infection.
  • •Diagnosis of an aneurysm in the chest, abdomen, or brain.
  • •Psychological or social characteristics that would interfere with their ability to fully participate in the study.

研究组 & 干预措施

Inspiratory Muscle Training (IMT) group

Experimental

The test protocol requires participants to inhale maximally (maximum inspiratory pressure, MIP) against 2mm diameter leak and sustain inhalation (sustained maximal inspiratory pressure, SMIP) until task failure. Participants will complete 3 SMIP maneuvers with each training session and use the best of the three for that day's training template (corresponding to about 80% SMIP for the IMT group) via the PrO2Fit software. Participants must match or exceed the SMIP template with each increasing level of the work-rest ratio. Work at each level consists of 6 breaths, 36 breaths total. If six breaths are completed, the next level starts. Rest intervals will progressively shorten as training continues from 40-seconds to 5-seconds. The session will be terminated if participants are unable to match at least 90% of the training template for two consecutive breaths or have completed all 36 breaths. Training will be done 4 times a week, and over 8-weeks.

干预措施: PrO2 Fit (IMT Trainer) (Device)

Sham Inspiratory Muscle Training (Sham-IMT) group

Sham Comparator

Similar to the IMT group protocol, participants will be required to complete 3 SMIP maneuvers with each training session. Participants will use the best of the three for that day's training template (corresponding to about 30% SMIP for the Sham-IMT group) via the PrO2Fit software. Participants must match or exceed the SMIP template with each increasing level of the work-rest ratio. Work at each level consists of 6 breaths, 36 breaths total. If six breaths are completed, the next level starts. Rest intervals will progressively shorten as training continues from 40-seconds to 30-, 20-, 15-, 10-, and 5-seconds. The training session will be terminated if participants are unable to match at least 90% of the training template for two consecutive breaths or have completed all 36 breaths. Training will be done 4 times a week, and over 8-weeks.

干预措施: PrO2 Fit (IMT Trainer) (Device)

结局指标

主要结局

Duration

时间窗: Baseline, within 48 hours of completing intervention

Duration, reported in seconds, to reach 63% of steady-state V̇O2 during a fixed-workload treadmill task. This technique is performed using breath-by-breath open-circuit spirometry and captures the V̇O2 fast component occurring in the transition from standing rest to treadmill walking.

次要结局

  • Distance Traveled(Baseline, within 9 days of completing intervention)

研究者

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

Stephen J. Carter, Ph.D.

Assistant Professor

Indiana University

研究点 (1)

Loading locations...

相似试验