CAP'Onco : Psychological and Social Consultation of Professional Accompaniment in Oncology
NCT ID: NCT03302767
Last Updated: 2021-05-04
Study Results
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View full resultsBasic Information
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COMPLETED
NA
29 participants
INTERVENTIONAL
2017-08-07
2018-06-27
Brief Summary
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* A weekly pluridisciplinary consultation in tandem (Social worker + Psychologist / Neuropsychologist)
* Monthly information meetings and workshops (TIC'Onco reunions: collective information times and Cogit'Onco workshops: cognitive workshops
* An information booklet "Prepare the work return" The aim of this research is to evaluate efficiency in term of quality of life improvement linked to work status, utility, feasibility and patients' satisfaction.
The aim of this research is to evaluate efficiency in term of quality of life improvement linked to work status, utility, feasibility and patients' satisfaction.
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Detailed Description
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* Cancer and survival: challenges for cancer patients who want to work while being treated
* Cancer and career: Job instability for cancer patients
* Difficulties and isolation of patients due to a lack of coordination between healthcare professionals and colleagues/management
* Post-treatment cognitive troubles stress and hindered patient return to employment: chemo brain This research-action will propose and evaluate a concrete device: To maintain a professional activity with the support of CAP'Onco during treatment, to balance between quality of life, managing the "cancer event" and the psychosocial consequences for professional experience, to provide an early, durable and multimodal support to improve work keeping and anticipate return to employment
Conditions
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Study Design
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NA
SINGLE_GROUP
SUPPORTIVE_CARE
NONE
Study Groups
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Psychological and Social Consultation
Psychological and Social Consultation
Psychological and Social Consultation
Psychological and Social Consultation at Baseline, during the study and at the end of follow-up
Interventions
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Psychological and Social Consultation
Psychological and Social Consultation at Baseline, during the study and at the end of follow-up
Eligibility Criteria
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Inclusion Criteria
* Informed Consent signed.
* Patients affiliated to a French social
* living in Gironde
* Professional activity at the time of diagnosis
* Treated for - breast cancer, Hodgkin's or non-Hodgkin's lymphoma (non-cerebral), testicular cancer
* CURATIVE support
* At any time during treatment (chemotherapy or radiotherapy, or immunotherapy)
Exclusion Criteria
* History of cancers
* Cerebral pathology and / or brain metastasis
25 Years
55 Years
ALL
No
Sponsors
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Institut Bergonié
OTHER
Responsible Party
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Principal Investigators
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Véronique GERAT-MULLER, PhD
Role: PRINCIPAL_INVESTIGATOR
Institut Bergonié - Supportive Oncology Care
Locations
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Institut Bergonié
Bordeaux, , France
Countries
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Provided Documents
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Document Type: Study Protocol and Statistical Analysis Plan
Other Identifiers
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2017-A01251-52
Identifier Type: OTHER
Identifier Source: secondary_id
IB2017-03
Identifier Type: -
Identifier Source: org_study_id
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