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Clinical Trials/NCT02318459
NCT02318459
Completed
Not Applicable

High Intensity Interval Training for thE Rehabilitation of Geriatric Patients - a Feasibility Pilot studY.

University Hospital, Geneva1 site in 1 country100 target enrollmentMay 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Muscle Weakness
Sponsor
University Hospital, Geneva
Enrollment
100
Locations
1
Primary Endpoint
Proportion of patients who complete the rehabilitation program
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

This is a pilot study for evaluating the feasibility of using High Intensity Interval Training in geriatric hospitalized patients compared to the standard current rehabilitation practice.

Detailed Description

High Intensity Interval Training (HIIT) has shown a superior effectiveness and efficiency when compared to Moderate Intensity Continuous Training (MICT) in several types of patients and in healthy subjects. There are no data on HIIT in a general geriatric population. This study is a pilot study evaluating the feasibility of using HIIT in geriatric hospitalized patients compared to the standard current rehabilitation practice without HIIT. It is our desire to perform a larger randomized comparative trial between HIIT and MICT if the pilot study proves its feasibility.

Registry
clinicaltrials.gov
Start Date
May 2014
End Date
February 2016
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Jean-Luc Reny

Head of division, Internal medicine and rehabilitation Trois-Chêne

University Hospital, Geneva

Eligibility Criteria

Inclusion Criteria

  • Patients aged 65 years and older hospitalized for rehabilitation after an acute medical condition
  • Expected duration of the rehabilitation ≥ 2 weeks
  • Ability to follow instructions to perform a Timed up and Go Test
  • Ability to perform exercises
  • Willing to participate in 4 sessions of HIIT per week for 2 weeks

Exclusion Criteria

  • Any acute condition with tachycardia, hypotension or fever.
  • Abnormal cycle ergometer stress test with
  • significant ECG modification
  • decrease of more than 20 mmHg of the blood pressure with exercise
  • ST depression at a workload \<6 METs
  • Inability to reach an intensity of 15/20 in the Borg's scale of perceived exertion
  • Any unresolved acute medical or surgical condition of the following kind:
  • acute heart failure
  • acute coronary syndrome \< 1 month
  • strole \< 1 month

Outcomes

Primary Outcomes

Proportion of patients who complete the rehabilitation program

Time Frame: 2 weeks

Secondary Outcomes

  • Distance walked in the 6MWT(2 weeks)
  • Muscle strength assessed for the upper and lower extremities(2 weeks)
  • Step variability changes as a measure of quality of ambulation(2 weeks)

Study Sites (1)

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