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A Reminder App to Reduce Radiation Dermatitis Rates in Patients With Head-and-Neck Cancer (RAREST-02)

Primary Purpose

Radiation Dermatitis, Radiation-induced Oral Mucositis

Status
Unknown status
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
mobile application (reminder app)
Sponsored by
University Hospital Schleswig-Holstein
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Radiation Dermatitis focused on measuring Head-and-neck cancer, radiotherapy, radiation dermatitis, oral mucositis, reminder app

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Histologically proven squamous cell carcinoma of the head-and-neck (SCCHN)
  • Indication for definitive or adjuvant radio(chemo)therapy
  • Possession of and ability to use a smart phone
  • Age ≥18 years
  • Written informed consent
  • Capacity of the patient to contract

Exclusion Criteria:

  • Nasopharynx cancer
  • Pregnancy, Lactation
  • Treatment with epidermal growth factor receptor (EGFR)-antibodies (either given or planned)
  • Expected non-compliance

Sites / Locations

  • Medical Practice for Radiotherapy and Radiation OncologyRecruiting
  • Dept. of Radiation Oncology, University of LübeckRecruiting
  • Department of Radiation Oncology, Cruces University Hospital/ Biocruces Health Research Institute
  • Dept. of Radiation Oncology, Hospital Universitario y Politecnico La Fe,

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Standard Care supported by a Reminder App (Arm A)

Standard Care alone (Arm B)

Arm Description

Treatment with Standard Care supported by a Reminder App, starting at the beginning of radiotherapy.

Treatment with Standard Care alone, starting at the beginning of radiotherapy.

Outcomes

Primary Outcome Measures

Rate of radiation dermatitis grade ≥2
at least moderate radiation-induced skin toxicity such as erythema and desquamation

Secondary Outcome Measures

Rate of radiation dermatitis grade ≥2
at least moderate radiation-induced skin toxicity such as erythema and desquamation
Rate of radiation dermatitis grade ≥3
severe radiation-induced skin toxicity such as erythema and desquamation
Pain score
Pain within the radiation fields measured with a self-rating analogue scale ranging from 0 (no pain) to 10 (maximum pain) points; higher values represent worse outcomes.
Rate of radiation-induced oral mucositis grade ≥2
at least moderate radiation-induced inflammation of the oral mucosa
Rate of radiation-induced oral mucositis grade ≥3
severe radiation-induced inflammation of the oral mucosa

Full Information

First Posted
September 27, 2019
Last Updated
November 2, 2020
Sponsor
University Hospital Schleswig-Holstein
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1. Study Identification

Unique Protocol Identification Number
NCT04110977
Brief Title
A Reminder App to Reduce Radiation Dermatitis Rates in Patients With Head-and-Neck Cancer
Acronym
RAREST-02
Official Title
RAdiotherapy RElated Skin Toxicity: A Reminder App to Reduce Radiation Dermatitis Rates in Patients With Head-and-Neck Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
November 2020
Overall Recruitment Status
Unknown status
Study Start Date
October 10, 2020 (Actual)
Primary Completion Date
November 2021 (Anticipated)
Study Completion Date
November 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Hospital Schleswig-Holstein

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The goal of this randomized trial is to investigate whether the addition of a reminder app to standard care leads to a reduction of dermatitis and oral mucositis during radio(chemo)therapy for locally advanced squamous cell carcinoma of the head-and-neck (SCCHN). The primary endpoint is the rate of patients experiencing grade ≥2 radiation dermatitis at 60 Gy of radiotherapy. 80 patients are required per arm within the full analysis set. Taking into account that 5% of patients will not qualify for full analysis set, 168 patients should be randomized. If the addition of a reminder app to standard care will result in a significant reduction of radiation toxicity, it could become a helpful tool for these patients.
Detailed Description
The goal of this trial is to investigate whether the addition of a reminder app to standard care leads to a reduction of dermatitis and oral mucositis during radio(chemo)therapy for locally advanced squamous cell carcinoma of the head-and-neck (SCCHN). This is a randomized, active-controlled, parallel-group trial, which will compare the following treatments of radiation dermatitis (primary endpoint) and oral mucositis in patients with SCCHN: Standard care supported by a reminder app (Arm A) vs. standard care alone (Arm B). The primary endpoint is to investigate the rate of patients experiencing grade ≥2 radiation dermatitis at 60 Gy of radiotherapy, the minimum planned total dose for all patients receiving definitive or adjuvant radiotherapy for locally advanced SCCHN with curative intention. In addition, the following endpoints will be evaluated: Radiation dermatitis grade ≥2 at the end of radiation treatment (EOT), radiation dermatitis grade ≥3 at 60 Gy and EOT, quality of life, pain, and radiation-induced oral mucositis grade ≥2 and grade ≥3 at 60 Gy and at EOT. According to sample size calculations, 80 patients are required per arm within the full analysis set. Taking into account that 5% of patients will not qualify for full analysis set, 168 patients should be randomized. The impact of the reminder app will be considered clinically relevant, if the rate of grade ≥2 radiation dermatitis can be reduced from 85% to 65%. If the addition of a reminder app to standard care will result in a significant reduction of radiation dermatitis and oral mucositis, it could become a helpful tool for patients during radiotherapy of for SCCHN.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Radiation Dermatitis, Radiation-induced Oral Mucositis
Keywords
Head-and-neck cancer, radiotherapy, radiation dermatitis, oral mucositis, reminder app

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
randomized, active-controlled, parallel-group trial
Masking
None (Open Label)
Allocation
Randomized
Enrollment
168 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Standard Care supported by a Reminder App (Arm A)
Arm Type
Experimental
Arm Description
Treatment with Standard Care supported by a Reminder App, starting at the beginning of radiotherapy.
Arm Title
Standard Care alone (Arm B)
Arm Type
Active Comparator
Arm Description
Treatment with Standard Care alone, starting at the beginning of radiotherapy.
Intervention Type
Device
Intervention Name(s)
mobile application (reminder app)
Intervention Description
This app will remind the patients four times a day to perform skin and mouth care. Instructions are given how to properly perform skin and mouth care. The patients may postpone each required care procedure for up to 2 hours. Finally, the patients are asked to state for each procedure whether or not they performed it. To increase the patients' motivation, they will earn points for each successfully performed care procedure.
Primary Outcome Measure Information:
Title
Rate of radiation dermatitis grade ≥2
Description
at least moderate radiation-induced skin toxicity such as erythema and desquamation
Time Frame
until 60 Gy of radiotherapy
Secondary Outcome Measure Information:
Title
Rate of radiation dermatitis grade ≥2
Description
at least moderate radiation-induced skin toxicity such as erythema and desquamation
Time Frame
at the end of radiotherapy
Title
Rate of radiation dermatitis grade ≥3
Description
severe radiation-induced skin toxicity such as erythema and desquamation
Time Frame
at 60 Gy of radiotherapy and at the end of radiotherapy
Title
Pain score
Description
Pain within the radiation fields measured with a self-rating analogue scale ranging from 0 (no pain) to 10 (maximum pain) points; higher values represent worse outcomes.
Time Frame
prior to radiotherapy, weekly during radiotherapy, at 60 Gy and at the end of radiotherapy
Title
Rate of radiation-induced oral mucositis grade ≥2
Description
at least moderate radiation-induced inflammation of the oral mucosa
Time Frame
at 60 Gy of radiotherapy and at the end of radiotherapy
Title
Rate of radiation-induced oral mucositis grade ≥3
Description
severe radiation-induced inflammation of the oral mucosa
Time Frame
at 60 Gy of radiotherapy and at the end of radiotherapy

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Histologically proven squamous cell carcinoma of the head-and-neck (SCCHN) Indication for definitive or adjuvant radio(chemo)therapy Possession of and ability to use a smart phone Age ≥18 years Written informed consent Capacity of the patient to contract Exclusion Criteria: Nasopharynx cancer Pregnancy, Lactation Treatment with epidermal growth factor receptor (EGFR)-antibodies (either given or planned) Expected non-compliance
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Dirk Rades, Professor
Phone
+49 451 500
Ext
45400
Email
dirk.rades@uksh.de
First Name & Middle Initial & Last Name or Official Title & Degree
Carlos A Narvaez
Phone
+49 451 500
Email
carlos.narvaez@uksh.de
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dirk Rades, Professor
Organizational Affiliation
Dept. of Radiation Oncology, University of Lübeck, Germany
Official's Role
Principal Investigator
Facility Information:
Facility Name
Medical Practice for Radiotherapy and Radiation Oncology
City
Hannover
State/Province
Niedersachsen
ZIP/Postal Code
30449
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Stefan Janssen, Priv.-Doz.
Email
st-janssen@gmx.net
Facility Name
Dept. of Radiation Oncology, University of Lübeck
City
Lübeck
State/Province
Schleswig-Holstein
ZIP/Postal Code
23562
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dirk Rades, Professor
Phone
+49 451 500
Ext
45400
Email
dirk.rades@uksh.de
First Name & Middle Initial & Last Name & Degree
Carlos A Narvaez
Phone
+49 451 500
Ext
45401
Email
carlos.narvaez@uksh.de
Facility Name
Department of Radiation Oncology, Cruces University Hospital/ Biocruces Health Research Institute
City
Barakaldo
State/Province
Vizcaya
Country
Spain
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jon Cacicedo, MC
Email
JON.CACICEDOFERNANDEZBOBADILLA@osakidetza.eus
Facility Name
Dept. of Radiation Oncology, Hospital Universitario y Politecnico La Fe,
City
Valencia
Country
Spain
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Antonio J Conde, MD
Email
antoniojconde@gmail.com

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
32450921
Citation
Rades D, Narvaez CA, Doemer C, Janssen S, Olbrich D, Tvilsted S, Conde-Moreno AJ, Cacicedo J. Radiotherapy-related skin toxicity (RAREST-02): A randomized trial testing the effect of a mobile application reminding head-and-neck cancer patients to perform skin care (reminder app) on radiation dermatitis. Trials. 2020 May 25;21(1):424. doi: 10.1186/s13063-020-04307-0.
Results Reference
derived

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A Reminder App to Reduce Radiation Dermatitis Rates in Patients With Head-and-Neck Cancer

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