Impact of Adapted Aesthetic Onco in Patients With Upper Aerodigestive Tract Cancer During Their Management
NCT ID: NCT06959810
Last Updated: 2025-09-17
Study Results
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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NOT_YET_RECRUITING
NA
55 participants
INTERVENTIONAL
2025-09-16
2028-09-15
Brief Summary
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Initial feedback from patients who have been able to benefit from adapted oncoesthetics (OEA) is overwhelmingly positive.
This study will assess the feasibility of oncoesthetics and describe any obstacles.
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Detailed Description
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The French association for Oncological Support Care (SOS) defines socio-aesthetics as "the professional practice of aesthetic care adapted to people who are fragile or suffering as a result of an attack on their physical or psychological integrity, or in social distress". Priority patients for aesthetic care are those whose treatments have had an impact on body image (mutilating surgery, skin toxicities), and/or who are in a situation of social precariousness and suffer from a loss of self-esteem.
For patients suffering from VADS cancer, a population not usually in need of aesthetic care but in need of self-image restoration, an incentive program has been set up. Initial feedback from patients who have been able to benefit from adapted oncoesthetics (OEA) is overwhelmingly positive.
This study will assess the feasibility of OAS for VADS cancer patients, and describe any obstacles.
Conditions
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Study Design
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NA
SINGLE_GROUP
SUPPORTIVE_CARE
NONE
Study Groups
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Three sessions of Adapted Onco-Esthetics
Patients will received three sessions of Adapted Onco-Esthetics
Adapted Onco-Esthetics sessions
Patient will received three sessions of Adapted Onco-Esthetics
Interventions
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Adapted Onco-Esthetics sessions
Patient will received three sessions of Adapted Onco-Esthetics
Eligibility Criteria
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Inclusion Criteria
* Neoplastic location: oropharynx, oral cavity, hypopharynx, larynx, nasal cavity, salivary glands, cavum, sinus.
* Patient due to start oncological treatment (recurrence authorized)
* Patient fluent in French.
* Affiliation with a social security scheme
* Signature of informed consent prior to any specific procedure linked to the study
* Treatment with curative intent
Exclusion Criteria
* Any associated medical or psychological condition that could compromise the patient's ability to participate in the study
* Patient deprived of liberty, under guardianship, or subject to a legal protection measure or unable to express their consent.
* Patient unable to undergo trial follow-up for geographical, social or psychopathological reasons.
18 Years
ALL
No
Sponsors
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Fondation de France
OTHER
GIRCI NO
UNKNOWN
Centre Francois Baclesse
OTHER
Responsible Party
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Locations
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Centre Francois Baclesse
Caen, , France
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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OEUVRE
Identifier Type: -
Identifier Source: org_study_id
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