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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT05539378
Other study ID # BBCDS
Secondary ID
Status Enrolling by invitation
Phase N/A
First received
Last updated
Start date June 29, 2023
Est. completion date August 2026

Study information

Verified date May 2023
Source University Children's Hospital, Zurich
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to assess the link between sleep and the clearance of waste products from the brain. This will be assessed in a group of healthy older adults.


Description:

First, the investigators want to assess the relationship between sleep parameters and markers for brain clearance, assessed with MRI and blood samples. Second, the investigators want to probe whether associations can be influenced by modulation of sleep parameters by means of auditory stimulation.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 40
Est. completion date August 2026
Est. primary completion date June 2026
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 50 Years to 80 Years
Eligibility Inclusion Criteria: - Participation in previous longitudinal cohort studies at the study site - Ability to provide written and verbal informed consent - Fluency in the German language - Stable home situation that allows for reliable application of the intervention for the duration of the study - Ability to apply the intervention for the duration of the study, either alone or with support from a co-habitant - For women: Hormonal contraception, if menstrual cycle is still present or has been present within a year - Good general health status, normal cognitive function Exclusion Criteria: - Failure or inability to give informed consent - Inability to follow the procedures of the investigation - For women: pregnancy or breastfeeding - Presence of sleep disorders (e.g. sleep apnoea, narcolepsy, restless leg syndrome, insomnia, rapid eye movement (REM) sleep disorder) - Shift-work or a home situation that requires several awakenings during the night (e.g. newborn) - History of serious illness likely to interfere with study outcomes - Presence or history of a diagnosed neuropsychiatric illness - Current diagnosis of uncontrolled or poorly controlled diabetes - Current cancer of the brain or unstable cancer undergoing treatment - Evidence of serious atherosclerotic cardiovascular disease

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Auditory Stimulation
enhancement of sleep slow wave activity through acoustic stimulation
Sham (no stimulation)
Playing no tones during sleep but still recording brain activity

Locations

Country Name City State
Switzerland Institute for Regenerative Medicine, University Hospital Zurich Zurich

Sponsors (2)

Lead Sponsor Collaborator
University Children's Hospital, Zurich University of Zurich

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Correlation between EEG slow wave activity (uV) and cerebrospinal fluid flow (ml/min) from phase contrast MRI 2 weeks
Primary Correlation between EEG slow wave activity (uV) and diffusivity (mm2/s) from diffusion MRI 2 weeks
Primary Correlation between EEG slow wave activity (uV) and perfusion (ml/min/100 ml) from arterial spin labelling MRI 2 weeks
Primary Correlation between EEG slow wave activity (uV) and beta-amyloid (pg/ml) 2 weeks
Primary Correlation between EEG slow wave activity (uV) and tau (pg/ml) 2 weeks
Secondary Correlation between EEG slow wave activity (uV) and fatigue, assessed via the fatigue severity scale (FSS) questionnaire 2 weeks
Secondary Correlation between EEG slow wave activity (uV) and sleepiness, assessed with the Epworth Sleepiness Scale questionnaire 2 weeks
Secondary Correlation between EEG slow wave activity (uV) and memory function, assessed with the Hopkins Verbal Learning Test (memory score) 2 weeks
Secondary Correlation between EEG slow wave activity (uV) and attention, assessed with the Trail Making Test (time to completion) 2 weeks
Secondary Correlation between EEG slow wave activity (uV) and C-Reactive Protein (mg/L), assessed from a blood sample 2 weeks
Secondary Correlation between EEG slow wave activity (uV) and TNF-alpha (pg/L), assessed from a blood sample 2 weeks
Secondary Correlation between EEG slow wave activity (uV) and interleukins (pg/L), assessed from a blood sample 2 weeks
Secondary Correlation between EEG slow wave activity (uV) and executive function (summary score, dimensionless) 2 weeks
Secondary Correlation between EEG slow wave activity (uV) and neuro-metabolite levels (mmol) from magnetic resonance spectroscopy 2 weeks
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