Sleep quality under temperature change
Conditions
Interventions
Group 1: 1 night Technogel, 1 week break, 1 night standard
Group 2: 1 night standard, 1 week break, 1 night Technogel
Sponsors
Charité Campus Charité Mitte
Eligibility
Sex/Gender
Male
Age
45 Years to 65 Years
Inclusion criteria
Inclusion criteria: Written consent of study aprticipants after oral and written information
Exclusion criteria
Exclusion criteria: Known sleep disorder requiring treatment substance or alcohol abuse acute-of chronic disease requiring treatment treatment with hypnotic medications influencing the sleep-wake center known slow digestive speed, obstipation known diverticuli/ intestinal obstructions previous complicated abdominal surgery Acute or chronic intestinal disease planned MRI within the study participation period
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Changes of core body temperature, as well as body surface and mattress surface temperature (temperature measurement by Vitalsense Core Temp. Capsule (Hidalgo Ltd., Cambridge, UK), as well as furface temperature sensors "iButtons", Maxim, Dallas, USA) | — |
Secondary
| Measure | Time frame |
|---|---|
| Changes in phsyiological parameters (hear rate, EEG-Frequencies by polysomnographic measurement, Embla PSG system) | — |
Countries
Germany
Contacts
Public ContactSebastian Herberger
Interdisziplinäres Schlafmedizinisches Zentrum der Charité
Outcome results
None listed