Het onderzoek heeft geen betrekkinig op een specifieke aandoening. Het onderwerp van de simulatie is menstruatiepijn, maar het onderzoek heeft betrekking op de methodologie. nvt
Conditions
Interventions
None listed
Sponsors
NIVEL
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: Participants have to be women with an age between 18 and 45.
Exclusion criteria
Exclusion criteria: Inability to have an unaided conversation in Dutch Knowing the interviewer who performs the simulated medical consultation No experience at all with menstrual pain
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The study's primary parameters are affective, physiological and cognitive responses measured as state anxiety, psycho-physiological arousal as measured with skin conductance responses and outcome expectations about the the simulated illness in the interview. The study endpoint is the concordance of these measures between 1) subjects participating in the interview and subjects re-viewing their own interview and 2) between subjects participating in an interview and other participants (not participating in any interview) viewing interviews of others. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary study parameters are heart rate, positive and negative affect and illness perceptions about the simulated illness in the interview. Demographic variables, health status, trust in healthcare, communication preferences and empathic ability will be measured as control variables. | — |
Countries
Netherlands
Outcome results
None listed