Cognitive Impairment Clinical Trial
Official title:
Predictive Value of the Distress Thermometer as a Predictive Screening Instrument to Detect Cancer-related Cognitive Impairment in Cancer Patients
Cognitive impairment associated with chemotherapy is an important reported post-treatment
side-effect among breast and other cancer survivors. As some patients report cognitive
complaints before the administration of their therapy, some authors suggest an association
with psychological risk factors such as distress. Distress, a multifactorial unpleasant
emotional experience of a psychological (cognitive, behavioral and emotional), social and/or
spiritual nature that may interfere with the ability to cope with cancer effectively, its
physical symptoms and its treatment, can easily be assessed by the Distress Thermometer.
In this trial we aim to determine if the Distress Thermometer, accompanied by the 38-item
Problem List, could predict cancer-related cognitive impairment in patients with hematologic
malignancies, and in patients with gynecological, urological, breast, lung or
gastro-intestinal cancer receiving curative radiotherapy, chemotherapy, radiochemotherapy,
anti-hormonal or targeted therapy.
Design: Prospective, observational study. All cancer patients of the above mentioned cancer types receiving an anticancer treatment with curative intent will be asked to participate to this study. Consenting patients will undergo serial assessment at baseline, and 6 months after inclusion. Patient will be screened by the Distress Thermometer and 38-item Problem List followed by a neuropsychological assessment and self-assessment tools. ;
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