Practices and Organizations Related to Emerging Occupations of Care (EPOCK) Coordination in Oncology (EPOCK)

June 18, 2020 updated by: University Hospital, Bordeaux

Pilot Observational and Analytic Study of Practices and Organizations Related to Emerging Occupations of Care Coordination in Oncology: Modeling the Concept of Care Coordination in Oncology (EPOCK)

Several stakeholders are implied in cancer care pathways and there is a need for coordinating their actions. New occupations of care coordination have thus emerged. However, the conditions of their efficiency have been too few reported and included discrepancies between reports. In this context, the main objective is to propose a modeling of care coordination and associated emerging occupations (nurse-based) by comparing theoretical expected outcomes to professionals, patients and caregivers representations.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

Several stakeholders are implied in cancer care pathways and there is a need to coordinate their actions. New occupations of care coordination have thus emerged, such as nurse coordinator in France (IDEC: Infirmière de Coordination). However, the conditions of their efficiency are not well known. Moreover, several other complementary approaches and nurse occupations have to be identified because of their contribution to care coordination (IDE TAS, IPO, IDE AMA, IDE-CO, IDE HAD-CAD, IDE ETP)*. Finally, all together, these interventions of care coordination appeared as complex and asked for a theoretical model. Because of this high variability of the practices, without an underlying model, the impact of care coordination on patient quality of life, safety and efficiency of care is difficult to assess. In this context, the main objective is to propose a modeling of care coordination and associated emerging occupations by comparing theoretical expected outcomes to professionals, patients and caregivers representations.

The pilot observational study is based on three distinct stages: (1) the definition of care coordination in oncology using a literature review and a Delphi consensus study; (2) the description of practices, contexts, perceptions and attitudes related to care coordination occupations in oncology using a qualitative and a cross-sectional quantitative survey; (3) the comparison of the practices to the theoretical model to propose a modeling of care coordination occupations in oncology.

Study Type

Observational

Enrollment (Actual)

960

Contacts and Locations

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

Study Locations

      • Avignon, France
        • Institut Sainte Catherine
      • Bordeaux, France
        • CHU de Bordeaux
      • Bordeaux, France
        • Clinique Tiivoli Ducos
      • Langon, France
        • CH Sud Gironde
      • Libourne, France
        • CH de Libourne
      • Paris, France
        • Institut Curie
      • Saint-Priest, France
        • Institut de Cancerologie de La Loire
      • Talence, France
        • HAD Bagatelle
      • Toulouse, France
        • Institut Claudius Regaud
      • Toulouse, France
        • CHU de Toulouse

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.

Eligibility Criteria

Ages Eligible for Study

18 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Four samples :

  • Professionals of cancer care coordination
  • Cancer patients
  • Family caregivers of the selected patients
  • Professionals working with professionals of care coordination

Description

Inclusion Criteria:

  • For health institutions: public or private institutions in which nurses contributing to care coordination. Each institution will be associated with one type of coordination occupation, even if other healthcare workers contribute to care coordination in the same institution.
  • For professionals of care coordination: nurses contributing to care coordination in oncology (IDEC , IDE TAS, IPO, IDE AMA, IDE-CO, IDE HAD-CAD or IDE ETP)
  • For professionals working with professionals of care coordination:

    • Medical and non-medical healthcare professionals (oncologist, surgeon, nurses…), administrative professionals (secretary…), professionals of supportive care (psychologists, social workers…) and volunteers in patient organizations.
    • Private practitioners: general practitioner, private nurses, pharmacist
  • For the patients : adults under supervision of the selected professionals of care coordination for at least four weeks and able to express themselves
  • For the caregivers: family caregivers of the selected patients.

Exclusion Criteria:

  • For health institutions: private healthcare networks, territorial support platforms, home-based care providers, healthcare houses
  • For professionals of care coordination: coordinating medical doctors of care networks, coordinating medical doctors of hospital care at home, practitioners of regional cancer networks.
  • For the patients: <18 years old

Study Plan

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

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Modeling of care coordination in Oncology in France
Time Frame: During the whole period (36 months: from Month 1 to Month 36)
Constitutive elements of modelling of care coordination in oncology in France (qualitative analysis)
During the whole period (36 months: from Month 1 to Month 36)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Care coordination profesionals quality of life
Time Frame: Quantitative cross sectional survey (from Month 10 to Month 29)
Three scores : perceived organizational support, role conflict and commitment to the organization
Quantitative cross sectional survey (from Month 10 to Month 29)
Satisfaction with care coordination for profes professionals working with professionals of care coordination
Time Frame: Quantitative cross sectional survey (from Month 10 to Month 29)
Score of satisfaction
Quantitative cross sectional survey (from Month 10 to Month 29)
Patients quality of life and satisfaction with care coordination
Time Frame: Quantitative cross sectional survey (from Month 10 to Month 29)
Score of satisfaction and score of quality of life (measured with the European Organization for Research and Treatment (EORTC) quality of life questionnaire)
Quantitative cross sectional survey (from Month 10 to Month 29)
Caregivers burden with care coordination
Time Frame: Quantitative cross sectional survey (from Month 10 to Month 29)
Score of burdean (Zarit Burden Interview) with care coordination
Quantitative cross sectional survey (from Month 10 to Month 29)
Caregivers satisfaction with care coordination
Time Frame: Quantitative cross sectional survey (from Month 10 to Month 29)
Score of satisfaction with care coordination
Quantitative cross sectional survey (from Month 10 to Month 29)

Collaborators and Investigators

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

Publications and helpful links

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

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 Major Dates

Study Start (ACTUAL)

April 17, 2018

Primary Completion (ACTUAL)

October 2, 2019

Study Completion (ACTUAL)

October 30, 2019

Study Registration Dates

First Submitted

November 9, 2017

First Submitted That Met QC Criteria

November 20, 2017

First Posted (ACTUAL)

November 22, 2017

Study Record Updates

Last Update Posted (ACTUAL)

June 19, 2020

Last Update Submitted That Met QC Criteria

June 18, 2020

Last Verified

June 1, 2020

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • CHUBX 2016/31

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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