obesity / adiposity E66
Conditions
Interventions
Group 1: Within-subject design:
Day 1: fMRI measurement with 160 IU intranasal placebo (0.27% m-cresol, 1.6% glycerol, 98.13% water) 8 puffs per nostril (1 x spray = 0.1 ml solution with 10 IU)
Day
Sponsors
Universitätsklinikum Hamburg-Eppendorf
Eligibility
Sex/Gender
All
Age
55 Years to No maximum
Inclusion criteria
Inclusion criteria: - MRI-compatible - Medical information and signed declaration of consent
Exclusion criteria
Exclusion criteria: -
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome is to survey the metabolic-cognitive control of eating decisions, long-term weight management of elderly participants, and their insulin function. The following data will be collected: Screening: - Blood samples (insulin parameters: peripheral). - Anthropometric measurements. - Questionnaires. - Generation of the individual stimulus set. Day 1 & Day 2: - Blood samples (insulin parameters: peripheral) - Anthropometric measurements. - Administration: insulin / placebo. - fMRI o Neurobehavioral data. o Insulin parameters (centrally). | — |
Countries
Germany
Contacts
Public ContactVivien Breckwoldt
Institut für Systemische Neurowissenschaften - Universitätsklinikum Hamburg-Eppendorf
Outcome results
None listed