Skip to main content
Clinical Trials/NCT06109896
NCT06109896
Not yet recruiting
Not Applicable

ONCO_STORIES. Stress, Trauma, Origins, Psychological Responses, Interpersonal Relationships and Experiences in the Clinical History of Cancer Patients

Fondazione Policlinico Universitario Agostino Gemelli IRCCS0 sites200 target enrollmentOctober 31, 2023
ConditionsTumor

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Tumor
Sponsor
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Enrollment
200
Primary Endpoint
Collect and analyze information from the multidimensional assessment of cancer patients
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief Summary

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.

Registry
clinicaltrials.gov
Start Date
October 31, 2023
End Date
December 31, 2028
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

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;

Outcomes

Primary Outcomes

Collect and analyze information from the multidimensional assessment of cancer patients

Time Frame: 1 hour

Descriptive and statistical analysis of data collected on the clinical and psychological conditions of the cancer patient through routine assessments and self-report questionnaires.

Similar Trials