Digital Solutions for bEtter cAre (ALTHEA)

European Institute of Oncology

Status

Enrolling

Conditions

Cancer Diagnosis

Treatments

Behavioral: Patients, survivors, caregivers, family members and healthcare professionals

Study type

Interventional

Funder types

Other

Identifiers

NCT07416513

L2-293

Details and patient eligibility

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.

Enrollment

200 estimated patients

Sex

All

Ages

12+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

HEALTHCARE PROFESSIONALS:

Healthcare professionals actually working in oncology and/or psychooncology;
Teachers of paediatric cancer patients.

ADULT POPULATION:

Patients with a current or previous cancer diagnosis
Adequate language proficiency,
Able to provide informed consent;

PAEDIATRIC POPULATION:

Older than 12 years of age;
Patients with a current or previous cancer diagnosis;
Adequate language proficiency;
Legal guardians of paediatric cancer patients able to provide informed consent.

CAREGIVERS:

Caregivers and/or family members of cancer patients who lived or assist the loved ones with a current or previous cancer diagnosis in the cancer journey;
Adequate language proficiency;
Able to provide informed consent;
Caregivers and/or family members of paediatric cancer patients under 12 years of age.

Exclusion criteria

Healthcare professionals with limited oncology patient contact;
Insufficient knowledge of the local language;
Severe cognitive impairment, and/or mental disorders that prohibited their participation in the study or inadequate verbal skills that may render them incapable of informed consent (as evaluated by the clinician);
Inability to understand the study materials (as evaluated by the clinician);
Physical or psychological impairment that prohibits their participation in focus groups (as evaluated by the clinician).