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

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

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05907551
Acronym
DERMOCOS
Enrollment
210
Registered
2023-06-18
Start date
2023-07-25
Completion date
2023-10-25
Last updated
2023-08-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neoplasms

Brief summary

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

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.

Interventions

OTHERQuestionnaires

25-items questionnaire

Sponsors

Institut de cancérologie Strasbourg Europe
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

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

Design outcomes

Primary

MeasureTime frameDescription
Describe patients' knowledges regarding cutaneous side-effects, nail and hair toxicities induced by anticancer drugsat inclusion4 items questionnaires
Describe patients' knowledges regarding dermo-cosmetics and aesthetic solutions that can attenuate cutaneous side-effects, nail and hair toxicities induced by anticancer drugsat inclusion10 items questionnaires

Secondary

MeasureTime frameDescription
Describe patients' socio-economic profile to assess equity regarding access to dermo-cosmetics and aesthetic solutionsat inclusion11 items questionnaires
Correlate patients' knowledge level depending on tumoral locationat inclusionTumoral location as described in medical chart
Correlate patients' knowledge level depending on received treatmentat inclusionType of chemotherapy administered on the day of inclusion as described in medical chart
Correlate patients' knowledge level depending on treatment phaseat inclusionType of treatment phase (i.e. neoadjuvant, adjuvant, 1st or 2nd metastatic line) as described in medical chart

Countries

France

Contacts

Primary ContactManon VOEGELIN
promotion-rc@icans.eu(0)3 68 33 95 23
Backup ContactClaire VIT
promotion-rc@icans.eu(0)3 88 25 85 29

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026