Adaptation of a Knowledges Exchange Portal Between (KEP) Healers and Patients : Obstacles and Sources to KEP Use for Breast Cancer Women (Sav-AQ)

September 3, 2019 updated by: University Hospital, Bordeaux

Adaptation of a Knowledges Exchange Portal (KEP) Between Healers and Patients : Study of Obstacles and Sources to the Use of a KEP in the Case of Women Affected by a Breast Cancer in Nouvelle Aquitaine(Sav-AQ)

The project is imbued with the whole problematic of patient follow-up and patient support, taking into account the experiences and needs of breast cancer patients. It concerns the dissemination of knowledge through the implementation of a specific clinical innovation designed to optimizing breast cancer patient pathway. The " Patients en réseau " association offers us to participate at the web platform evolution Mon Réseau Cancer du Sein in adapting it. The feasibility study focuses on (1) the platform utilization and (2) sources and obstacles to its utilization in the French context

Study Overview

Detailed Description

One of the French Cancer Plan 2014-2019 objectives is to improve the town-hospital coordination and information's exchange between professionals. This research project aims to reach this important objective of exchange development and the amelioration of the coordination concerning breast cancer women. Breast cancer requires the integration of aggressive treatments implying physical, psychological and social consequences. That's why an optimized care pathway needs a coordinated and multidisciplinary organization, and more particularly a personalized approach taking into account the whole patients' needs in physical, psychological and social perspectives. To reach this goal, it is important to support those patients, to answer their needs for a better disease management in their own health pathways. The research issues lie in this outcome.

The project is imbued with the whole problematic of patient follow-up and patient support, taking into account the experiences and needs of breast cancer patients. It concerns the dissemination of knowledge through the implementation of a specific clinical innovation designed to optimizing breast cancer patient pathway.

The " Patients en réseau " association offers us to participate at the web platform evolution Mon Réseau Cancer du Sein in adapting it. The feasibility study focuses on (1) the platform utilization and (2) sources and obstacles to its utilization in the French context

Study Type

Observational

Enrollment (Actual)

35

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

      • Bordeaux, France, 33000
        • Institut Bergonie

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

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

30 women with a breast cancer will participate to the study, they will represent a sufficient and realis effective considering the active list of treated patients with a breast cancer at the Bergonié Institute.

5 healers (one nurse, two doctors, a senior health manager, a manipulator in medical imaging)

Description

Inclusion criteria of patients :

  • Age ≥ 18 y.o;
  • With a diagnosis of breast cancer,
  • treated at the Bergonié Institute;
  • Patients who express a non-opposition to participate to SAVAQ research;
  • Patients who have an Internet access at home.

Inclusion criteria of healers :

- Doctors, Nurse, Senior health manager, Technologist medical imaging from the center participated to the research

Exclusion criteria of patients:

  • Patients with a severe psychiatric pathology (medical diagnosis);
  • Patients who doesn't speak French

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
Feasability of the web portal
Time Frame: Month 6

Number of connections to the portal each month:

  • Types of documents consulted
  • Types of downloaded documents
  • Types of documents sought
  • Connection duration
  • Number of connections
  • Number of comments / questions posted
  • Number of comments / questions viewed
  • Number of comments / questions sought
Month 6

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Number of the portal connections realized each month
Time Frame: Month 6
Number of the portal connections realized each month
Month 6
Number of webpages used
Time Frame: Month 6
Number of webpages used
Month 6
Number of status posted
Time Frame: Month 6
Number of status posted
Month 6
Number of comments/questions posted
Time Frame: Month 6
Number of comments/questions posted
Month 6
Number of "like" emoticon posted
Time Frame: Month 6
Number of "like" emoticon posted
Month 6
Number of "comfort" emoticon posted
Time Frame: Month 6
Number of "comfort" emoticon posted
Month 6
Number of "favorites" emoticon posted
Time Frame: Month 6
Number of "favorites" emoticon posted
Month 6
Number of "mood" posted
Time Frame: Month 6
Number of "mood" posted
Month 6
Number of private posts posted
Time Frame: Month 6
Number of private posts posted
Month 6
Number of webpages consulted
Time Frame: Month 6
Number of webpages consulted
Month 6
Number of leaflets consulted
Time Frame: Month 6
Number of leaflets consulted
Month 6
Headings of leaflets consulted
Time Frame: Month 6
Headings of leaflets consulted
Month 6
Number of cards consulted
Time Frame: Month 6
Number of cards consulted
Month 6
Headings of cards consulted
Time Frame: Month 6
Headings of cards consulted
Month 6
Number of videos consulted
Time Frame: Month 6
Number of videos consulted
Month 6
Headings of videos consulted
Time Frame: Month 6
Headings of videos consulted
Month 6
Number of address consulted in the address list
Time Frame: Month 6
Number of address consulted in the address list
Month 6
Number of upcoming events consulted
Time Frame: Month 6
Number of upcoming events consulted
Month 6

Collaborators and Investigators

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

March 16, 2018

Primary Completion (Actual)

June 17, 2019

Study Completion (Actual)

June 17, 2019

Study Registration Dates

First Submitted

January 31, 2018

First Submitted That Met QC Criteria

March 13, 2018

First Posted (Actual)

March 21, 2018

Study Record Updates

Last Update Posted (Actual)

September 4, 2019

Last Update Submitted That Met QC Criteria

September 3, 2019

Last Verified

September 1, 2019

More Information

Terms related to this study

Other Study ID Numbers

  • CHUBX 2016/19

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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