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Oral Chemotherapy and Quality of Care

Community and Hospital Experiences for Patients Treated by Oral Chemotherapy at the University Hospital of Caen: Analysis of the Process and Its Dysfunctions

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03561467
Acronym
PARCOURS
Enrollment
60
Registered
2018-06-19
Start date
2018-03-29
Completion date
2018-09-29
Last updated
2018-06-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer

Brief summary

PARCOURS is a non-interventional research study evaluating dysfunctions in the continuous city-hospital journey of a patients cohort treated by oral chemotherapy (60 patients followed for 3 months). References used are the National Cancer Institute recommendations for the oral chemotherapy treated outpatients. Parameters found are : information exchanged, ambulatory and hospital monitoring in case of adverse event and adherence to treatment. The study includes also a medico-economic evaluation (hospitalization and transport spending in case of dysfunction in the patient's journey). Deviations will be analyzed.

Interventions

OTHERObservational

Evaluation of dysfunctions in the continuous city-hospital journey of a patients cohort treated by oral chemotherapy

Sponsors

MSD France
CollaboratorINDUSTRY
University Hospital, Caen
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patient over 18 years old * Suffering from cancer (hematological malignancies, digestive tumors, thoracic tumors or cutaneous tumors) * With an oral anticancer chemotherapy initial prescription written by an oncologist or hematologist from the University Hospital of Caen, whatever the place of the drug dispensing (Community pharmacy or hospital pharmacy )

Exclusion criteria

\- Patient treated by oral anticancer chemotherapy for another pathology

Design outcomes

Primary

MeasureTime frameDescription
Number of dysfunctions3 monthsNumber of dysfunctions objectified during the 3-month follow-up period, by sub-processes of the course

Secondary

MeasureTime frameDescription
Adverse events3 monthsnumber
Expenses related to the use of unplanned hospital care3 monthsExpenses related to the use of unplanned hospital care during the follow-up period: number of oncologist consultations, transport spending, emergency rehospitalizations and additional examinations.
Satisfaction of the patientAt month 3RESOCAN questionnaire
Drug adherence3 monthsmeasured by Morisky-Green's questionnaire to the patient
Satisfaction of the local professionalsAt month 3RESOCAN questionnaire
Quality of life of patientsAt month 3QLQC 30
Satisfaction of the caregiverAt month 3RESOCAN questionnaire

Countries

France

Contacts

Primary ContactValérie CHEDRU-LEGROS, PhD
chedru-v@chu-caen.fr+332 31 06 46 66

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026