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

Sponsor
Institut de cancérologie Strasbourg Europe (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05907551
Collaborator
(none)
210
1
4
52.4

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Questionnaires

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.

Study Design

Study Type:
Observational
Anticipated Enrollment :
210 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Study in Patients With Solid Tumor Regarding Access to Dermo-cosmetics and Aesthetic Solutions
Anticipated Study Start Date :
Jun 30, 2023
Anticipated Primary Completion Date :
Oct 30, 2023
Anticipated Study Completion Date :
Oct 30, 2023

Arms and Interventions

Arm Intervention/Treatment
Patients with Digestive System Cancer

Other: Questionnaires
25-items questionnaire

Patients with Head and Neck Cancer

Other: Questionnaires
25-items questionnaire

Patients with Breast Cancer

Other: Questionnaires
25-items questionnaire

Patients with Nervous System Tumors

Other: Questionnaires
25-items questionnaire

Patients with Urological Cancer

Other: Questionnaires
25-items questionnaire

Patients with Lung Cancer

Other: Questionnaires
25-items questionnaire

Patients with Gynecologic Cancer

Other: Questionnaires
25-items questionnaire

Outcome Measures

Primary Outcome Measures

  1. Describe patients' knowledges regarding cutaneous side-effects, nail and hair toxicities induced by anticancer drugs [at inclusion]

    4 items questionnaires

  2. Describe patients' knowledges regarding dermo-cosmetics and aesthetic solutions that can attenuate cutaneous side-effects, nail and hair toxicities induced by anticancer drugs [at inclusion]

    10 items questionnaires

Secondary Outcome Measures

  1. Describe patients' socio-economic profile to assess equity regarding access to dermo-cosmetics and aesthetic solutions [at inclusion]

    11 items questionnaires

  2. Correlate patients' knowledge level depending on tumoral location [at inclusion]

    Tumoral location as described in medical chart

  3. Correlate patients' knowledge level depending on received treatment [at inclusion]

    Type of chemotherapy administered on the day of inclusion as described in medical chart

  4. Correlate patients' knowledge level depending on treatment phase [at inclusion]

    Type of treatment phase (i.e. neoadjuvant, adjuvant, 1st or 2nd metastatic line) as described in medical chart

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Institut de cancérologie Strasbourg Europe Strasbourg France 67033

Sponsors and Collaborators

  • Institut de cancérologie Strasbourg Europe

Investigators

  • Study Chair: Nelly ETIENNE-SELLOUM, PharmD, Institut de cancérologie Strasbourg Europe

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Institut de cancérologie Strasbourg Europe
ClinicalTrials.gov Identifier:
NCT05907551
Other Study ID Numbers:
  • 2023-001
  • 2023-A00546-39
First Posted:
Jun 18, 2023
Last Update Posted:
Jun 22, 2023
Last Verified:
Jun 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Jun 22, 2023