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Recruiting Not applicable

Dermatitis During Adjuvant Irradiation for BREAst Cancer:

NCT06483477 · tracked via the Priya Life Science Denmark tracker
Phase
Not applicable
Started
2024-12-23
Last updated
2025-01-16

Condition(s) studied

Breast Cancer Female

Investigational drug(s) / intervention(s)

Standard skin careReminder App

Standard skin care: From the start of radiotherapy, standard skin care has to be performed by the patient. This may vary at the participating centers. At the site in Lübeck, it includes fatty cream with 2-10% urea (fatty cream alone, if patients do not tolerate urea) and, in case of pruritus, addition of mometasone furoate cream. In case of grade ≥2 moist desquamation or grade ≥3 radiation dermatitis, each day antiseptic agents will be administered for wound cleansing followed by administration of silicon or calcium alginate bandage. This treatment will be continued until moist desquamation radiation disappears and radiation dermatitis improves to grade 2. Fatty cream with 2-10% urea is applied to the irradiated skin four times daily. Mometasone furoate cream: In addition to the fatty cream with 2-10% urea, mometasone furoate cream (solution 0.1%) is applied to the irradiated skin once daily.

Reminder App: In addition to standard skin care, patients are supported by a Reminder App. The purpose of the app is to remind the patients in an intuitive, unobtrusive and supportive way to perform skin care. By default, patients are reminded four times a day, but they will also be able to define a notification schedule that best suits their personal needs. The patients may postpone each required care procedure for up to 2 hours. With each procedure, the patients are guided through the skin care with simple and self-explanatory illustrations. To increase the patients' motivation, they will additionally earn points for regular and punctual performed care procedures. The patients receive a hand-out including instructions how to properly perform skin care, but they can also find an information page within the application that includes similar instructions.

Study summary

In the randomized DAI-BREAC trial, a reminder app will be prospectively tested that reminds breast cancer patients four times each day to perform the required skin care. This will likely contribute to the reduction of grade ≥2 radiation dermatitis in these patients. A total of 268 patients will be randomized to receive standard skin care supported by a reminder app (Arm A) or standard skin care alone (Arm B). Stratification will be done using the three factors treatment volume, radiation boost, and at least one risk factor of dermatitis. Secondary aims include pain (radiation fields), patient satisfaction with the reminder app (Arm A only), impact of the app on the use of health technology (Arm A only), and benefit from support by staff members of the treating Department of Radiation Oncology and/or the UKSH academy regarding the use of the app (Arm A only).

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. Histologically proven invasive breast cancer 2. Indication for adjuvant hypo-fractionated radiotherapy 3. Possession of and ability to use a smartphone 4. Female gender 5. Age ≥18 years 6. Written informed consent 7. Capacity of the patient to contract Exclusion Criteria: 1. Pregnancy, Lactation 2. Expected non-compliance

Primary outcome measure(s)

  • Prevention of grade ≥2 radiation dermatitis — through study completion, an average of 4 weeks
    Radiation dermatitis will be assessed according to CTCAE v5.0.

Trial sites (5)

FacilityCityRegionStatus
Vejle Hospital, University Hospital of Southern Denmark Vejle Southern Denmark Not Yet Recruiting
Medical Practice for Radiotherapy and Radiation Oncology Hanover Lower Saxony Not Yet Recruiting
Medical School Hamburg, Schwerin Campus Schwerin Mecklenburg-Vorpommern Not Yet Recruiting
Malteser Hospital St. Franziskus Flensburg Schleswig-Holstein Not Yet Recruiting
Department of Radiation Oncology, University of Lübeck and University Medical Center Schleswig-Holstein Lübeck Germany Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06483477 on ClinicalTrials.gov ↗ ← All trials in Denmark