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The acute effects of sitting and breaking-up sitting on cognitive function in healthy elderly.

The acute effects of sitting and breaking-up sitting on cognitive function in healthy elderly. - Clinical MindSed trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON46706
Enrollment
22
Registered
2018-02-06
Start date
2018-04-23
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

Sedentary behaviour

Interventions

Participants will have four measurement days, in which they will be asked to sit for three hours uninterruptedly during two of these days. The other two days they will be asked to stay seated for th

Sponsors

Radboud Universitair Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - 70-90 years of age - Mentally able to give informed consent - Adequate visual and auditory acuity to complete neuropsychological testing - Scores on the MoCA of *24 - Able to sit for three hours uninterruptedly (no urinary urgency problems)

Exclusion criteria

Exclusion criteria: - Persons who are not physically able to perform light-intensity physical activity such as standing and walking. - Diagnosis of AD, any other type of dementia or MCI - History of familial early-onset dementia; first or second degree family member diagnosed with dementia aged *55 years of age - Enrolment in any investigational drug study - Diagnosis of or drug use for any major psychiatric disorder (a clinical diagnosis of major depressive disorder, bipolar or schizophrenia) e.g. Anti-depressants, anti-psychotics, lithium - Drug use that affects alertness from the evening before the measurement, till the end of the measurement day, e.g. Psycho pharmacy e.g. benzodiazepines (oxazepam, temazepam, zolpidem), over-the-counter medication (melatonine, valeriane) - Past history or MRI evidence of brain damage, including significant trauma, stroke, hydrocephalus, mental retardation, or serious neurological disorder - Vigorously active for more than 3 hours per week (based on SQUASH questionnaire)

Design outcomes

Primary

MeasureTime frame
The main parameter of this study is the difference between the conditions between the change in cognitive measures, as measured by the TAP test before and after the three hour periods. Alertness, working memory, and flexibility will be measured.

Secondary

MeasureTime frame
Cerebrovascular autoregulation will serve as an intermediate outcome. Changes in cerebral autoregulation and cerebrovascular reactivity will be measured before and after each of the 3 hour conditions as well.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)