Screening for Social Weaknesses and Coordination Course of Cancer Patients

NCT ID: NCT02369783

Last Updated: 2016-02-26

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

71 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-07-31

Study Completion Date

2015-02-28

Brief Summary

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The main objective of the study is to validate a methodology with Psychometric tool to measure levels of patients social fragility.

This tool will be dematerialized on a tablet. The answers will be then processed by a decision support algorithm, which automatically send an alert to detection of social fragility of the patient to the nurse navigators.

Detailed Description

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Conditions

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Cancer

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

SCREENING

Blinding Strategy

NONE

Study Groups

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Questionnaire and interview

The patient complete the questionnaire on the tablet to better know their social situation and any difficulties. Then, he will be interview during thirty minutes with a social worker and a nurse navigator. At the end of this intervention we will be offered to the patient monitoring and appropriate resources to its situation.

Group Type EXPERIMENTAL

Questionnaire and interview

Intervention Type OTHER

The aim is to detect social fragility.

Interventions

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Questionnaire and interview

The aim is to detect social fragility.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* All new patients enter ICLN for a diagnosis of cancer
* Patients who can read French or patients who can not read French, but accepting the translation by a close friend or family
* Patient having signed a free and informed consent

Exclusion Criteria

* Refusal of participation, major patients protected under guardianship.
* Patient can not read French without possibility of translation by a close friend or family
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Institut de Cancérologie de la Loire

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Franck Chauvin, PhD-MD

Role: STUDY_DIRECTOR

INSTITUT DE CANCEROLOGIE DE LA LOIRE

Locations

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Institut de Cancerologie de la Loire

Saint-Priest-en-Jarez, , France

Site Status

Countries

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France

Other Identifiers

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2014-05

Identifier Type: -

Identifier Source: org_study_id

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