Actively Recruiting
Digital Solutions for bEtter cAre
Led by European Institute of Oncology · Updated on 2026-02-18
200
Participants Needed
5
Research Sites
85 weeks
Total Duration
On this page
Sponsors
E
European Institute of Oncology
Lead Sponsor
E
European Union
Collaborating Sponsor
AI-Summary
What this Trial Is About
The target population includes cancer patients, caregivers, family members, healthcare providers and mental health specialists, who will be the primary end-users of the Althea platform. For patients, survivors, caregivers, and family members, the sample variables include age, gender, type and stage of disease, and time since the first diagnosis. The healthcare professionals that will be involved in this study are those who attend to oncological patients, with sample variables such as age, gender, professional role, and prior experience and training in oncology or psycho-oncology.
CONDITIONS
Official Title
Digital Solutions for bEtter cAre
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Healthcare professionals working in oncology and/or psycho-oncology
- Teachers of pediatric cancer patients
- Patients with a current or previous cancer diagnosis
- Adequate language proficiency
- Able to provide informed consent
- Patients older than 12 years of age
- Legal guardians of pediatric cancer patients able to provide informed consent
- Caregivers and/or family members of cancer patients with current or previous diagnosis
- Caregivers and/or family members of pediatric cancer patients under 12 years of age
You will not qualify if you...
- Healthcare professionals with limited oncology patient contact
- Insufficient knowledge of the local language
- Severe cognitive impairment or mental disorders preventing participation
- Inadequate verbal skills preventing informed consent
- Inability to understand study materials
- Physical or psychological impairments preventing participation in focus groups
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 5 locations
1
Centre François Baclesse
Caen, France
Actively Recruiting
2
Saarland University
Homburg, Germany
Not Yet Recruiting
3
European Institute of Oncology
Milan, Italy, Italy, 20141
Not Yet Recruiting
4
National Cancer Institute
Vilnius, Lithuania
Not Yet Recruiting
5
Catalan Institute of Oncology
Barcelona, Spain
Not Yet Recruiting
Research Team
G
Gabriella Pravettoni, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
OTHER
Number of Arms
1
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