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临床试验/NCT04025385
NCT04025385Unknown不适用

High-Intensity-Interval-Training in Geriatric Rehabilitation - A Feasibility Study

Klinik Valens1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2019年7月30日最近更新:
适应症
干预措施

试验速览

阶段
不适用
发起方
入组人数
60
试验地点
1
主要终点
Will there be a change in outcome of individuals vO2max?

研究概览

简要总结

Study with Patients (40-60 participants) above the age of 65. There will be a comparison of regular training on ergometer (10 trainings within 2 weeks, 40 min each) to high intensity interval training on ergometer (6 trainings within 2 weeks, 25 min each). At the beginning and at the end will be a spiroergometer to measure the individual limits and vO2max, which will be compared amongst the two groups. To receive a subjective feedback, there will be a series of questionnaires at the beginning, after one week and at the end. The goal of this study is to get more information about whether a HII-Training is feasible with elderly patients and whether they can profit form it.

研究设计

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

入排标准

年龄范围
65 Years 至 —(Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •cardiopulmonal resilient
  • •able to sit on a ergometer
  • •knowledge of German written and spoken

排除标准

  • •Severe cardiopulmonary restriction (LVEF <30%, conduction abnormalities from AV block IIb or higher)
  • •Absolute cardiopulmonary contraindications (acute coronary syndrome, unstable AP -> not capable of rehabilitation), uncompensated heart failure (dyspnea at rest, orthopnea, severe edema)
  • •No ischemic events (cardiac, cerebral, peripheral) within the last 3 months
  • •Severe pneumatological underlying disease: COPD GOLD 3 and higher or status after exacerbation within the last 2 weeks, Asthma grade 4
  • •Dyalisis reliant
  • •Severe psychiatric disorder (severe psychosis, severe depression)
  • •Distinct dementia

研究组 & 干预措施

Control Group

No Intervention

Patients will participate in regular training units

HIIT Group

Active Comparator

Patients will participate in high intensity interval training

干预措施: High Intensity Interval Training (Other)

结局指标

主要结局

Will there be a change in outcome of individuals vO2max?

时间窗: 2 Weeks

Measurement of vO2max with spiroergometer at the beginning and end

Is a High intensity interval training feasible with elderly patients in rehabilitation?

时间窗: 1 Day

Questionnaire (Clinic-intern questionnaire) amongst the involved personal

次要结局

  • Will there be a change in subjective quality of life?(2.5 Weeks)

研究者

发起方
Klinik Valens
申办方类型
Other
责任方
Principal Investigator
主要研究者

Michael Kruesi

Resident Physician, Doctoral Candidate

Klinik Valens

研究点 (1)

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