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Clinical Trials/NCT02893527
NCT02893527TerminatedNot Applicable

Implementation and Evaluation of a Social Journey Accompanied for Women With Breast Cancer Diagnosis

Institut du Cancer de Montpellier - Val d'Aurelle1 site in 1 country11 target enrollmentStarted: February 24, 2015Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Terminated
Sponsor
Enrollment
11
Locations
1
Primary Endpoint
Evaluate and compare the return to work rate

Study Overview

Brief Summary

Evaluate and compare the return to work rate at 12 months

Detailed Description

Evaluate and compare the return to work rate at 12 months (from J1C1 [first day of the first adjuvant chemotherapy regimen]) between the "intervention" group (which has accompanied the career) and the standard group course

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Patient major> 18
  • •Have a diagnosis of localized breast cancer requiring surgery immediately adjuvant therapy sequence including chemotherapy and radiotherapy
  • •Being more than 3 years of retirement at diagnosis
  • •Have a work contract valid at the time of diagnosis (before surgery)
  • •Do not practice a profession
  • •Be in possession of his rights (excluding guardianship, curatorship)
  • •Raise the general social security scheme and have rights to cash benefits in the Languedoc-Roussillon region

Exclusion Criteria

  • •Patient minor
  • •Patient diagnosed with metastatic breast cancer
  • •Patients refusing to sign the consent
  • •Patients do not have sufficient understanding of the French language
  • •Patients for whom it is impossible to give clear information

Arms & Interventions

Group "intervention"

Experimental

Personalized coaching coordinated by a coordinating nurse on a shutdown period of 8 months (consecutive stops).

Intervention: personalized coaching (Behavioral)

Group "standard"

No Intervention

conventional support

Outcomes

Primary Outcomes

Evaluate and compare the return to work rate

Time Frame: through study completion, an average of 5 years

Evaluate and compare the return to work rate at 12 months (from J1C1 \[first day of the first adjuvant chemotherapy regimen\]) between the "intervention" group (which has accompanied the career) and the standard group course

Secondary Outcomes

  • describe the conditions of the resumption of work(through study completion, an average of 5 years)

Investigators

Sponsor
Institut du Cancer de Montpellier - Val d'Aurelle
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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