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The PreventIT Feasibility RCT comparing two lifestyle-integrated exercise interventions delivered by use of ICT or an instructor with a control group in young older adults.

The PreventIT Feasibility RCT comparing two lifestyle-integrated exercise interventions delivered by use of ICT or an instructor with a control group in young older adults. - Protocol The PreventIT Feasibility RCT

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON45652
Enrollment
60
Registered
2016-12-22
Start date
2017-03-09
Completion date
Unknown
Last updated
2024-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Geriatrische aandoening, functieverlies gerontology old age

Interventions

The aLiFE intervention is a lifestyle-integrated functional exercise program adapted to young older adults. The eLiFE intervention is a lifestyle-integrated functional exercise programme to young ol

Sponsors

Vrije Universiteit
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: We will include community-dwelling adults aged 61-70 years, who have been retired for more than 6 months, are able to speak Dutch, are able to walk for 500 metres without walking aid and are available for home visits in the first 6 weeks following inclusion.

Exclusion criteria

Exclusion criteria: we exclude people that are too active (participating in exercise class > 1 time per week, or on their own * 150 minutes per week), that have travels planned for > 2 months during the intervention period, with cognitive impairment (MOCA

Design outcomes

Primary

MeasureTime frame
We will use two primary outcome measures: 1. Late-Life Function and Disability Instrument (LLFDI), to measure function and disability in the young older adults. 2. Complexity Metric, to assess behavioural complexity in the domains of physical activity, sleep, and social participation.

Secondary

MeasureTime frame
Various secundary parameters will be collected during the RCT.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)