Study in Patients With Solid Tumor Regarding Access to Dermo-cosmetics and Aesthetic Solutions

NCT ID: NCT05907551

Last Updated: 2023-08-22

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

UNKNOWN

Total Enrollment

210 participants

Study Classification

OBSERVATIONAL

Study Start Date

2023-07-25

Study Completion Date

2023-10-25

Brief Summary

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Cancer treatments can trigger cutaneous side-effects, as well as nail and hair toxicities. When related to drug treatment, this iatrogeny depends on the type of drug, its dosage and individual susceptibility. Although these dermatological adverse events are rarely serious, they can significantly alter patients' quality of life, and may even necessitate the introduction of curative treatment.

The impact of these side effects can be mitigated by the use of dermo-cosmetic products and aesthetic solutions. However, most of this supportive care is not reimbursed by the health insurance system, representing a source of inequalities in access to healthcare for cancer patients.

Detailed Description

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This study aims at establishing, in a cohort of patients with solid tumors, the state of their knowledges, given information and their financial capacities regarding access to dermo-cosmetics and aesthetic solutions, that are used in the attenuation of cancer treatments' side-effects.

Conditions

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Neoplasms

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Patients with Digestive System Cancer

Questionnaires

Intervention Type OTHER

25-items questionnaire

Patients with Head and Neck Cancer

Questionnaires

Intervention Type OTHER

25-items questionnaire

Patients with Breast Cancer

Questionnaires

Intervention Type OTHER

25-items questionnaire

Patients with Nervous System Tumors

Questionnaires

Intervention Type OTHER

25-items questionnaire

Patients with Urological Cancer

Questionnaires

Intervention Type OTHER

25-items questionnaire

Patients with Lung Cancer

Questionnaires

Intervention Type OTHER

25-items questionnaire

Patients with Gynecologic Cancer

Questionnaires

Intervention Type OTHER

25-items questionnaire

Interventions

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Questionnaires

25-items questionnaire

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Age \> 18 years
* Patients with solid tumors (eligible localization include: digestive system, Head and Neck, Breast, Brain, Lung Tumors, Urological and Gynecologic cancers)
* Patients able to read and understand French
* Patients that has expressed their consent and with signed consent form

Exclusion Criteria

* Minor or patients placed under guardianship or supervision
* Patients unable to read French
* Patients placed under judicial protection
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Institut de cancérologie Strasbourg Europe

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Nelly ETIENNE-SELLOUM, PharmD

Role: STUDY_CHAIR

Institut de cancérologie Strasbourg Europe

Locations

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Institut de cancérologie Strasbourg Europe

Strasbourg, , France

Site Status RECRUITING

Countries

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France

Central Contacts

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Manon VOEGELIN

Role: CONTACT

(0)3 68 33 95 23 ext. 33

Claire VIT

Role: CONTACT

(0)3 88 25 85 29

Facility Contacts

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Nelly ETIENNE-SELLOUM, PharmD

Role: primary

Other Identifiers

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2023-A00546-39

Identifier Type: OTHER

Identifier Source: secondary_id

2023-001

Identifier Type: -

Identifier Source: org_study_id

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