Door annelies_verachtert op Ma, 03/08/2015 - 10:30
In de loop der jaren is er een uitgebreid palet aan Psychosociale oncologische zorg (PSOZ) ontstaan. Naast het reguliere behandelaanbod binnen de PSOZ, zijn er altijd ontwikkelingen gaande en worden er nieuwe Psychosociale oncologische interventies (verder PSO-interventies) ontwikkeld. De praktijk wijst uit dat het niet altijd eenvoudig is om te ontdekken wàt er nu waar en voor wie aangeboden wordt: een overzicht van PSO-interventies ontbreekt.
Objective: The aim of this study is to co-create an evidence-based and theoretically informed web-based intervention (RESTORE) designed to enhance self-efficacy to live with cancer-related fatigue (CRF) following primary cancer treatment.
Advanced prostate cancer patients often undergo androgen deprivation therapy (ADT). Advanced disease and adverse ADT side effects are often debilitating and negatively impact mood. Social support has been shown to mitigate detrimental effects of stress on mood.
Objective: This study sought to characterize positive and negative mood in this select patient population and determine whether social support moderated relations between stress and mood.
Objective: Cancer-related fatigue (CRF) is one of the most common, persistent, and disabling symptoms associated with cancer and its treatment. Evidence-based treatments that are acceptable to patients are critically needed. This study examined the efficacy of mindfulness-based stress reduction (MBSR) for CRF and related symptoms.
Objective: This study aimed to understand factors related to post-traumatic growth (PTG) in patients who received allogeneic hematopoietic stem cell transplantation (HSCT), building baseline data for
developing intervention programs to enhance PTG in HSCT survivors.
Objectives: Cancer survivors often report cognitive problems. Furthermore, decreases in physical activity typically occur over the course of cancer treatment. Although physical activity benefits cognitive function
Objective: Our aim was to expand research on predictors of health-related quality of life (HRQOL) for adolescent and young adult survivors of childhood brain tumors who are not living independently by
evaluating the mediating role of family functioning in the association of disease severity/treatment late effects with survivor self-report and caregiver-proxy report of physical and emotional HRQOL.
Objective: Patient-reported outcome measures (PROMs) that assess the quality of patient-centred cancer care have failed to measure all six patient-centredness dimensions endorsed by the Institute
of Medicine (IOM). This study is the first to use the Quality of Patient-Centered Cancer Care (QPCCC) measure that covers all six IOM patient-centredness dimensions to examine haematological cancer survivors’ perceptions of care and characteristics associated with perceived quality of care.
Objective: The objective of this study is to assess the quality of life (QOL) of cancer patients and their family members over 1-year period post therapy.
