Breast Cancer Patients' Cognitive Symptoms After Information About Chemotherapy-Related Cognitive Symptoms (CONTEXT)
Breast Cancer, Cognitive Symptoms, Cognitive Decline
About this trial
This is an interventional supportive care trial for Breast Cancer focused on measuring Breast cancer, Chemotherapy, Cognitive symptoms, Self-affirmation, Health communication, Nocebo, Stereotype threat
Eligibility Criteria
Inclusion Criteria:
- Primary breast cancer diagnosis stage I-III
- Scheduled to receive (neo) adjuvant chemotherapy
- 18 years or older
- Sufficient command of the Dutch language
- Internet access
Exclusion Criteria:
- A history of neurological and psychiatric symptoms that influence cognitive functioning
- Previous cancer diagnosis
- Using drugs
- Drinking more than three alcoholic drinks a day
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
No Intervention
Experimental
Experimental
Control
Information without self-affirmation
Information with self-affirmation
Participants in the control group received standard information on treatment side-effects.
Before completing the study's online baseline survey (pre-chemotherapy), participants in the information group received standard information with additional written information about potential chemotherapy-related cognitive symptoms.
Before completing the study's online baseline survey (pre-chemotherapy), participants in the information+SA group (SA=self-affirmation) received standard and additional written information about potential chemotherapy-related cognitive symptoms with a subsequent self-affirmative text.