Clinical Stories and Psychological Experiences of Cancer Patients
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Self Report Questionaires.
- Who it may be relevant to
- Registry conditions: Tumor. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
ONCO_STORIES. Stress, Trauma, Origins, Psychological Responses, Interpersonal Relationships and Experiences in the Clinical History of Cancer Patients
Overview
The purpose of the study is to collect and analyze information from the multidimensional assessment of cancer patients (medical, psychological, psychometric, biological, etc.) treated at the Fondazione Policlinico Universitario Agostino Gemelli IRCCS. The collection of information will allow to investigate the possible presence of correlations between psychological aspects and clinical medical conditions of the person during the course/treatment of cancer. In the course of the study, the possible presence of previous stressful and/or traumatic events, and the presence of psychological, post-traumatic and/or dissociative symptoms during treatment will be explored. Any correlations between medical conditions and psychological, emotional and behavioral characteristics will also be explored. Finally, it will be possible to investigate the effectiveness of psychological interventions that are carried out according to clinical practice.
Interventions
- Other Self Report Questionaires
Collection and analysis of information from patient self-report assessments and integration with clinical information from assessments performed routinely during cancer treatment.
Primary outcome measures
- Collect and analyze information from the multidimensional assessment of cancer patients [Time frame: 1 hour]
Eligibility criteria
Inclusion criteria
- Individuals between 18 and 99 years old;
- Individuals with a diagnosis of current oncologic disease and in active oncologic treatment at the hospital where the study is conducted;
- Individuals with a history of oncologic disease who have completed oncologic treatment or in follow-up at the hospital where the study is conducted;
Exclusion criteria
- Non-signing of informed consent;
- Non-signing of consent/assent by patient/legal guardian;
- Patients with cognitive impairment or legal disqualification;
- Clinical/medical or psychological condition that does not allow completion of self-report questionnaires;
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT06109896 · 5913