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ImpaQt * Pilot study on cognitive performance levels of patients with chronic Q-fever or Q-fever Fatigue Syndrome

ImpaQt * Pilot study on cognitive performance levels of patients with chronic Q-fever or Q-fever Fatigue Syndrome - ImpaQt * Pilot study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON42926
Enrollment
100
Registered
2016-09-01
Start date
2016-11-21
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Q-fever

Interventions

Long Term Impact
Memory
Q-fever

Sponsors

Universitair Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

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

MeasureTime frame
Main study parameters/endpoints: The main study parameters will be cognitive performance, measured with several neuropsychological tests

Secondary

MeasureTime frame
-

Countries

The Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)