Supporting Resilience and Case Finding
Not yet recruiting
- Conditions
- Psychological distressCancer patientsAnxietyDepressionPsychologische distressKankerpatiëntenAngstDepressie
- Registration Number
- NL-OMON26756
- Lead Sponsor
- VUmc-GGZ inGeestPO Box 74077, 1070 BB Amsterdam
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 240
Inclusion Criteria
• Patients with cancer, treated at the VU University Medical Center (VUmc), department of Medical Oncology (clinic and day treatment)
• Patients are enrolled, using a proportional stratified consecutive sample based on the cancer diagnoses in the population at the department of Medical Oncology. Each stratum is represented in the sample (both in the ‘before’ and ‘after’ phase) in the same proportion as in the population at the department of Medical Oncology
Exclusion Criteria
• Age < 18 or > 85 years
• Second opinion
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary outcome is the recognition of psychological distress after introduction of the new procedure. The diagnostic accuracy of the new procedure (study aim v-a) is determined by comparing information in the medical/nursing record about the presence of psychological distress with patient reported psychological distress (Distress Thermometer + Problem List, HADS). Sensitivity, specificity, false positives, false negatives, and positive and negative predictive value are determined.
- Secondary Outcome Measures
Name Time Method