The Effectiveness of the Screening Inventory of Psychosocial Problems (SIPP) in Cancer Patients
NCT00859768 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 568
Last updated 2011-03-08
Summary
The purpose of this study is to evaluate the effectiveness and feasibility of the Screening Inventory of Psychosocial Problems (SIPP) in consultation settings with respect to early recognition and treatment of psychosocial distress, communication between patients and physicians, and psychological distress and quality of life in cancer patients treated with radiotherapy (RT).
Conditions
- Breast Cancer
- Lung Cancer
- Prostate Cancer
- Bladder Cancer
- Cervix Cancer
- Cancer of Endometrium
- Cancer of Skin
- Non-Hodgkin Lymphoma
- Colorectal Cancer
Interventions
- OTHER
-
Questionnaire administration
The patient receives the SIPP at two different time points during their RT period. The first time point is before the first consultation with the radiotherapist (before starting RT) and the second time point is before the last consultation with the radiotherapist at the end of the RT period. At both time points, the SIPP is handed over to the radiotherapist at the start of the consultation. The radiotherapist screens the scores of the SIPP to get an overview of potential psychosocial problems and patient's needs of psychosocial care.
Sponsors & Collaborators
-
Dutch Cancer Society
collaborator OTHER -
Maastricht University Medical Center
collaborator OTHER -
Institute Verbeeten
collaborator OTHER -
Maastro Clinic, The Netherlands
collaborator OTHER -
Netherlands Open University
lead OTHER
Principal Investigators
-
Lilian Lechner, PhD · Netherlands Open University, Faculty of Psychology
-
Gertrudis I Kempen, PhD · Maastricht University, Faculty of Health, Medicine, and life Sciences, Department of Health Care and Nursing Science, School for Public Health and Primary Care (CAPHRI)
Study Design
- Allocation
- RANDOMIZED
- Purpose
- SUPPORTIVE_CARE
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2008-04-30
- Primary Completion
- 2010-10-31
- Completion
- 2010-10-31
Countries
- Netherlands
Study Locations
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