Actively Recruiting

Age: 70Years +
All Genders
ID07211334

Comparison of the Effects of High-Intensity Interval Training Versus Moderate-Intensity Continuous Training in Frail Elderly People

Led by University Hospital, Grenoble · Updated on 2026-05-05

92

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to evaluate and compare the effects of different types of physical exercise on frail elderly people aged 70 and older. The study focuses on reversing functional decline and improving cardiorespiratory fitness in this population, which is at risk of loss of independence and reduced quality of life. Frailty is identified using specific criteria including weight loss, sedentary lifestyle, fatigue, slow walking speed, and lack of strength. The project compares two exercise methods used at the Health and Sport Center of Grenoble Alpes University Hospital: high-intensity interval training (HIIT) and moderate-intensity continuous training (MICT).

CONDITIONS

Brief Title

High Intensity Interval Training Versus Moderate Intensity Continuous Training in Frail Elderly

Who Can Participate

Age: 70Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 70 or older
  • Meet at least one of five frailty criteria according to Fried
  • Do not object to the analysis of anonymized data
  • Affiliated with social security
  • Able to use an ergocycle safely
  • Medically stable with no acute illness or recent worsening that could be aggravated by exercise (physician's discretion)
Not Eligible

You will not qualify if you...

  • Unstable medical conditions that may be worsened by physical activity (physician's discretion)
  • Musculoskeletal disorders or severe neurocognitive conditions preventing safe use of ergocycle or participation
  • Currently participating or recently participated in other interventional studies that could affect results
  • Protected persons such as pregnant women, breastfeeding mothers, persons deprived of liberty, or under legal protection measures

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - 24 weeks

Participants are observed while following either a high-intensity interval training (HIIT) or moderate-intensity continuous training (MICT) exercise program, combined with therapeutic education workshops to support independence and motivation for physical activity.

Two to three supervised in-person sessions per week for the first 8 weeks, followed by monthly follow-up contacts for the next 16 weeks

Follow-up

Duration - After 24 weeks

Participants continue to be monitored for maintenance of physical activity and assessed on various health and functional outcomes.

Assessments at weeks 8 and 24 including physical fitness, frailty criteria, body composition, quality of life, sleep quality, and motivation

Trial Site Locations

Total: 1 location

1

University Grenoble alpes

Grenoble, France, 38043

Actively Recruiting

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Research Team

F

Flore PATRICE

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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