PreventIT enhanced Lifestyle-integrated Functional Exercise programme pilot study

Completed

• Conditions: Geriatrische aandoeningen, functieverlies; gerontology; old age

• Registration Number: NL-OMON43240
• Lead Sponsor: Vrije Universiteit

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 28 February 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 5

Inclusion Criteria

We will include community dwelling adults between 60 and 70 years of age. Only participants with ability to walk 500 metres without walking aids will be included.

Exclusion Criteria

Exclusion criteria include cognitive impairment (Montreal Cognitive Assessment, MOCA *24 points) and self-reported cardiovascular, pulmonary, neurological, and mental disease where exercise is contraindicated, any changes in health condition the past 6 months (stroke, cancer in need of treatment, severe neurological diseases that affect physical function, COPD (Gold 3 and 4), and heart failure (NYHA 3 and 4)). The target population of eLiFE is not the most fit of the young older adults. Excluded are therefore those who are attending organised exercise classes more than twice a week and/or those who are exercising more than 1 hour on their own each week.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Semi-structured questionnaire, focus group and workshop for evaluating<br /><br>usability and feasibility of eLiFE.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Late-Life Function and Disability Instrument. </p><br>