Type of Study:

Interventional

Study Design:

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Supportive Care

Outcome Measure:

Patients' score on the EORTC-INFO26 module15 questionnaire, measuring ´Satisfaction with information provision´, right after initial treatment

Outcome Description:

Evaluating satisfaction with information on different areas of the disease, diagnosis, treatment and care. It contains the following scales: (a) Information about the disease; (b) Information about medical tests; (c) Information about treatment; (d) Information on other services, and single items: (a) Written information; (b) Information on CDs or tape/video; (c) Satisfaction with the amount of information; (d) Desire for more information; (e) Desire for less information; (f) Helpfulness of information.

Outcome Time Frame:

Right after initial treatment (t0)

Safety Issue:

No

Principal Investigator

Lonneke V van de Poll-Franse, Dr

Investigator Role:

Principal Investigator

Investigator Affiliation:

Tilburg University, The Netherlands

Authority:

Netherlands: Medical Ethics Review Committee (METC)

Study ID:

UVT 2010-4743

NCT ID:

NCT01185626

Start Date:

April 2011

Completion Date:

April 2014

Related Keywords:

• Ovarian Cancer
• Endometrium Cancer
• patients
• Ovarian Neoplasms
• Endometrial Neoplasms