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Integrated Care Pathway in Oncology (PASSION)


2020-02-21


2022-12-31


2022-12-31


1800

Study Overview

Integrated Care Pathway in Oncology (PASSION)

A centralized unit for integrated management of care pathway in Oncology has been created. This unit settles the patients' appointments (biopsy, intravenous device, chemotherapy, imaging, oncologist...). The aim of this study is to assess the delay between the first appointment with the oncologist and the beginning of the antitumoral treatment, and therefore evaluate the efficacy of the care pathway unit. The second aim is to assess the satisfaction of patients and health care teams.

PASSION is a french monocentric study. For the retrospective cohort, patient will be selected through the use of data warehouse available on the HEGP. For the prospective cohort, patient will be included according to the selection criteria. Each patient will be followed up during 6 month and a satisfaction questionnaire will be completed at 1 month and 4 month of the first administration of anti-tumor therapy. For both cohort, clinical-anatomo-biological data will be collected through the use of data warehouse available on the HEGP.

  • Colon Cancer
  • Gastric Cancer
  • Pancreatic Cancer
  • Thoracic Neoplasms
  • Breast Cancer
  • Ovarian Cancer
  • Bladder Cancer
  • Prostate Cancer
  • BEHAVIORAL: Care pathway unit
  • APHP190973

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates Results Reporting Dates Study Record Updates

2019-12-02  

N/A  

2022-05-12  

2020-01-17  

N/A  

2022-05-13  

2020-01-22  

N/A  

2022-05  

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

Design Details

Primary Purpose:
N/A


Allocation:
N/A


Interventional Model:
N/A


Masking:
N/A


Arms and Interventions

Participant Group/ArmIntervention/Treatment
: Historic cohort

Retrospective cohort of patients that were treated in the Hôpital Européen Georges Pompidou before the creation of the care pathway unit.

: Prospective cohort

All consecutive patients that meet the inclusion criterion and will begin a cancer care after the study start.

BEHAVIORAL: Care pathway unit

  • Patients from the prospective cohort will have their health care scheduled by the care pathway unit.
Primary Outcome MeasuresMeasure DescriptionTime Frame
Time between the first appointment with the oncologist and the beginning of antitumoral treatment.Delay of health care6 months
Secondary Outcome MeasuresMeasure DescriptionTime Frame
Patients satisfactionSatisfaction of patients with OUT-PATSAT35 questionnaire (out-patient satisfaction) : Likert type scale with 5 ordered modalities (bad to excellent), rated from 1 to 5.6 months
Health care teams satisfactionSatisfaction of health care teams : qualitative questionnaire with 4 ordered modalities (very satisfied to not satisfied)6 months
Rate of emergency consultations and hospitalizationsNeed for unexpected health care6 months

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person’s general health condition or prior treatments.

Ages Eligible for Study:
ALL

Sexes Eligible for Study:
18 Years

Accepts Healthy Volunteers:

    Inclusion Criteria:

  • Histologically proven : colon, gastric, pancreatic, prostate, bladder, breast, thoracic, or ovarian cancer
  • First appointment for cancer care at the Hôpital Européen Georges Pompidou
  • Intravenous antitumoral treatment

  • Exclusion Criteria:

  • Medical care non covered by social welfare
  • Radiochemotherapy
  • Death in the 6 months following first oncological appointment or absence of medical care in the year following the first oncological appointment

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

  • MSD France

  • PRINCIPAL_INVESTIGATOR: Virginie Bichon, AP-HP, Hôpital Européen Georges Pompidou, Paris

Publications

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

No publications available