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Clinical Trials/NCT03320161
NCT03320161
Completed
Not Applicable

A Patient Consensus for the Research in Supportive Care in French Cancer Care Centers: the CyPRES Project

UNICANCER57 sites in 1 country604 target enrollmentOctober 10, 2018
ConditionsCancer Patients

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cancer Patients
Sponsor
UNICANCER
Enrollment
604
Locations
57
Primary Endpoint
Supportive care listed and prioritized by patients
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

In oncology a number of supportive care therapies are proposed to patients. This study will identify the different therapies and prioritize these therapies from the patients' perspectives. This study will provide a framework for optimizing supportive care strategies and identifying those therapies that need to be validated by clinical trials.

Detailed Description

In oncology, supportive care should be used along with curative treatment or palliative care in order to improve patients' health-related quality of life, overall survival and to better support treatment side effects as well as the disease evolution. Unfortunately, they are not widely used in clinical practice. A direct assessment of the needs perceived unmet by patients could allow to assess the magnitude of expectations to better target treatments as example. A prospective assessment of the expectations and needs of the patients is thus essential. This would also allow help to highlight the convergence between supportive care proposed and used and those expected by patients. The first step to understanding how to optimize the use of resources and to improve the quality of care is to identify patient's expectations. Moreover, it is now well recognized that patients should play a key role in the research and that their active participation in research can increase the relevance of the research. In this context, the CyPRES project aims to: 1. assess through national consensus the patients' expectations in terms of supportive care in order to help both clinicians and health care services; 2. prioritize them and to arrange resources according to priority needs identified; 3. identify supportive care for which no previous research (evidence-based medicine) has demonstrated their usefulness. A randomized clinical trial will thus be proposed; 4. Involve patients in the written, conduct and analyses, as well as communications of the randomized clinical trial.

Registry
clinicaltrials.gov
Start Date
October 10, 2018
End Date
May 26, 2021
Last Updated
4 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
UNICANCER
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • patients supported for cancer
  • patients of ERI, Espaces Ligue (french cancer care centers) or patient associations
  • patients aged at least 18 years old

Exclusion Criteria

  • Not applicable

Outcomes

Primary Outcomes

Supportive care listed and prioritized by patients

Time Frame: 4 to 7 months after inclusion

Prioritize supportive care therapies: completion of questionnaire N°2 Expectations and needs of the patients questionnaire n°2 completed

Study Sites (57)

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