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临床试验/NCT05287243
NCT05287243Unknown不适用

The Impact of a Customized Respiratory Muscle Training and Maintenance Program on Cardiopulmonary Function in People With Parkinson's Disease.

University of St. Augustine for Health Sciences2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2022年11月1日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
40
试验地点
2
主要终点
maximum inspiratory pressure

研究概览

简要总结

People with PD have lower cardiopulmonary function than their age matched peers. This decline can further impair a person's ability to participate in exercise and daily activities.

Furthermore, the limitations in cardiopulmonary function can have a severe impact on mortality. There is evidence indicating the positive changes IMT can have on cardiopulmonary function in people with PD. Through intensive daily exercise people with PD have shown improvements in maximum inspiratory pressure and maximum expiratory pressure though detraining does occur when the intervention is not continued. The purpose of the proposed study is to determine if improvements in expiratory muscle strength can be maintained with a maintenance inspiratory muscle training program. The hypothesis is that there will be a significant change from baseline at the three and six month follow ups.

详细描述

Testers will complete the following outcome measures at the pretest: height, weight, maximum inspiratory pressure, maximum expiratory pressure, heart rate, blood pressure, respiratory rate, six-minute walk test, and Fatigue Impact Scale in person.17,18 Participants, and caregivers if necessary, will be educated on how to complete the intensive IMT program. The dosage will be IMT 3 times/day for 20 repetitions each with resistance set at 30% of baseline maximum for 12 weeks. This training will occur at home.

Participants will record daily their completion of the intensive IMT. Investigators will contact participants weekly for follow-up of compliance and questions. Participants will be contacted either through email, text, or phone call, depending on their preference.

After 12 weeks of intensive IMT training, the investigators will complete the first posttest which will include the following assessments: maximum inspiratory pressure, maximum expiratory pressure, heart rate, blood pressure, respiratory rate, six-minute walk test, and fatiguability scale in person.

Participants, and caregivers if necessary, will be educated on the maintenance IMT program. The dosage for the maintenance program will be 33% of their intensive IMT program, which will result in IMT 1 time/day for 20 repetitions with resistance set at 30% of baseline maximum at the first posttest. The participants will continue the maintenance program for 12 more weeks.

Participants will record daily their completion of the maintenance IMT program. Investigators will contact participants weekly for follow-up of compliance and questions. Participants will be contacted either through email, text, or phone call, depending on their preference.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
30 Years 至 99 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • physician's diagnosis of Parkinson's disease

排除标准

  • people who are actively smoking, have a pacemaker, recent diagnosis of chronic obstructive pulmonary disease, bronchial asthma, active pulmonary disease within 1 month, or hospitalization within 2 months of time of study

结局指标

主要结局

maximum inspiratory pressure

时间窗: 5 minutes

measure of the maximum inspiratory cardiopulmonary pressure

Fatigue Impact Scale

时间窗: 10 minutes

measure of a person's self report fatigue, ranges from 0-36 and higher score indicates greater impact of fatigue

6 minute walk test

时间窗: 8 minutes

distance walked in 6 minutes

respiratory rate

时间窗: 1 minute

breaths per minute

maximum expiratory pressure

时间窗: 5 minutes

measure of the maximum expiratory cardiopulmonary pressure

blood pressure

时间窗: 1 minute

measure of rest blood pressure

heart rate

时间窗: 1 minute

heart beats per minutes

次要结局

未报告次要终点

研究者

发起方
University of St. Augustine for Health Sciences
申办方类型
Other
责任方
Principal Investigator
主要研究者

Kristen Barta

Associate Professor

University of St. Augustine for Health Sciences

研究点 (2)

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