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Differential physiological and cognitive effects of an increase in daily physical activity as generated by the COACH method in healthy elderly APOE-e4 carriers and non-carriers

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON22568
Enrollment
266
Registered
2016-06-29
Start date
2016-08-01
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

EN: Alzheimer's Disease, Inactivity, ApoE-e4, genetic vulnerability for Alzheimer's Disease NL: ziekte van Alzheimer, dementie, inactiviteit, ApoE-e4 dragerschap, genetische kwetsbaarheid voor Alzheimer

Interventions

INTERVENTION The intervention studied is the COACH method, a 12 week pedometer based exercise counseling strategy, aimed at enhancing low-to-moderate daily physical activity. The method is based on t
Miller & Rollnick, 1991
Rubak, Sandbaek, Lauritzen, & Christensen, 2005). Six individual coaching sessions will be scheduled to guide the individual in assessing and obtaining personal activity goals. Five sessions are sched
Calfas et al., 1996). All coaching sessions in the trajectory of the participants will be performed by the same coach. CONTROL Participants in the control group receive 5 individually guided muscle

Sponsors

Clinical Neuropscyhology section, Vrije Universiteit Amsterdam
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: In order to be eligible to participate in this study, participants must meet all of the following criteria: age ≥ 55 years; able to perform the Timed Up & Go Test with or without assistive device, and a Mini Mental State Examination (Folstein, Folstein, & McHugh, 1975) score higher than 25. Both males and females will be included. In the second part of the study only those participants who display low levels of physical activity as measured in Part 1 of the study are recruited.

Exclusion criteria

Exclusion criteria: A potential subject who meets any of the following criteria will be excluded from participation in this study: wheelchair bound, cardiovascular problems that limit physical activity, epilepsy, presence of neurodegenerative disorder or focal neurological deficit, diagnosis of dementia or mild cognitive impairment, progressive or terminal disease, depression, history of alcoholism, severe visual problems, severe auditory problems and problems with the Dutch language.

Design outcomes

Primary

MeasureTime frame
Main outcome measure is cognitive function, measured with neuropsychological tests.

Secondary

MeasureTime frame
Secondary outcome measures are physical functioning measured with performance-based field tests, IGF-1 and BDNF serum levels and ADLs, mood and quality of life, measured by questionnaires

Contacts

Public ContactSara Galle

van der Boechorststraat 1 room 1F-62

s.a.galle@vu.nl0031205988769

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)