Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT05402488

Exploring the Recovery Function of Sleep in Neurodegeneration

Led by University of Zurich · Updated on 2022-06-02

200

Participants Needed

1

Research Sites

220 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The overall objective of this study is to identify the best approach for assessing the recovery function of sleep in neurodegenerative diseases associated with abnormal protein aggregation with regard to the conception of future intervention studies. To this end, the investigators will follow an exploratory approach in a preferably broad data set collected in patients with neurodegenerative diseases associated with abnormal protein aggregation and in healthy humans.

CONDITIONS

Official Title

Exploring the Recovery Function of Sleep in Neurodegeneration

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Good general health or confirmed diagnosis of neurodegenerative disease associated with abnormal protein aggregation along international criteria
  • Age above 18 years
  • In ambulant setting: ability to apply the ambulant EEG device for the duration of the study, either alone or with help of co-habitant if MoCA < 20
Not Eligible

You will not qualify if you...

  • Failure to give informed consent
  • Inability to follow the procedures of the study, e.g. due to language problems or cognitive deficits
  • Known or suspected non-compliance, drug- or medication abuse
  • Inability to hear the tones to be applied during sleep in auditory stimulation experiments
  • Skin disorders/problems/allergies in face/ear area that could worsen with electrode application
  • Regular intake of drugs that may alter the relationship between sleep and outcome variables under investigation (opioids, benzodiazepines and z-drugs (nonbenzodiazepines))
  • Clinically significant concomitant disease states
  • Too high (disease) burden for patients
  • Additional non-medical exclusion criteria may be defined for certain cognitive tasks (e.g. no glasses during experiments involving eye tracking)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University Hospital Zurich, Neurology department

Zurich, Canton of Zurich, Switzerland, 8091

Actively Recruiting

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Research Team

A

Angelina Maric, Dr. phil.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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