breast cancer maligne mamma-carcinoom
Conditions
Interventions
Stuy 1: observation-design: focus groups and interviews
Study 2: experiment: 4 video-vignettes are viewed .
Add-on study: 1 video-vignette is viewed.
Sponsors
NIVEL
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: Study 1 + 2: breast cancer survivors: women between 18-65, minimally 5 years disease-free, speak fluent Dutch, members of Dutch Breast Cancer Organisation. healthy women: women between 18 and 65, speak fluent Dutch. add-on study: healthy women between 18-65, fluent in Dutch
Exclusion criteria
Exclusion criteria: Study 1 + 2: breast cancer survivors: less than 5 years disease free. healthy women: women who are cancer survivors.;Add-on study: women who are cancer survivors.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Study 1: Qualitative data - opinions concerning the disclosure of a palliative prognosis and the role of hope and explicitness herein. Study 2: Experiment: anxiety- and uncertainty reduction Add-on study: Emotional arousal and recall are the main study parameters of this pilot study. Emotional arousal will be measured with physiological responses (heart rate and skin conductance). Recall is assessed as the number of correctly recognized or recalled information elements (both primed and free recall) will be measured. | — |
Secondary
| Measure | Time frame |
|---|---|
| Study 2: Experiment: satisfaction, self efficacy Focusgroups: qualitative data - opinions concerning the specific communication elements. Add-on study: same as main study. Extra: positive & negative affect. | — |
Countries
Netherlands
Outcome results
None listed