Q-fever
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients with chronic Q-fever or Q-fever Fatigue Syndrome and controls from the general population. The pilot study will be performed in a subgroup of patients and controls who gave consent in a previous study (ImpaQt study, CCMO * Nijmegen number *2015-1919*).
Exclusion criteria
Exclusion criteria: Patients with clinical depression (as measured with the Beck*s Depression Index in the ImpaQt study) will be excluded. Participants with medical conditions that cause cognitive dysfunction, (dementia, CVA or other brain injuries, etc .) as well as a history of major psychiatric disorders, will also be excluded.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Main study parameters/endpoints: The main study parameters will be cognitive performance, measured with several neuropsychological tests | — |
Secondary
| Measure | Time frame |
|---|---|
| - | — |
Countries
The Netherlands