cognitieve stoornis cognitive impairment out of hospital cardiac arrest
Conditions
Interventions
The participant will receive sham iTBS. The participant is not aware what type
of stimulation he/she receives. Directly after stimulation the participant is
asked to perform the N-back task on a com
Sponsors
Universiteit Maastricht
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: - You are between 18 and 75 years old - You have had a cardiac arrest from three months to five years before the start of the study
Exclusion criteria
Exclusion criteria: -being pregnant -A medical history of a neurological condition that may affect memory beyond cardiac arrest -Having a metal implant in or close to the head - Have a medical history with epilepsy or a family member who has it. - Have a pacemaker or ICD
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The main study outcomes are performance on the N-back task with regard to accuracy. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary study parameters: -Reaction time in milliseconds. -Changes in an individuals ability to detect signals expressed as sensitivity (d*), where d* = z(false alarm rate) - z(hit rate). Other study parameters include: - Information regarding the cardiac arrest (date cardiac arrest, the cause, length of hospital stay). - personal information (sex, age, level of education, working hours and profession). - performance on the Stroop, Digit span, and trail making test during the screening. | — |
Countries
Netherlands
Outcome results
None listed