Clinical Stories and Psychological Experiences of Cancer Patients

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

200 participants

Study Classification

OBSERVATIONAL

Study Start Date

2023-10-31

Study Completion Date

2028-12-31

Brief Summary

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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.

Detailed Description

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Conditions

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Tumor

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

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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.

Intervention Type OTHER

Eligibility Criteria

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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;

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Responsible Party

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Responsibility Role SPONSOR

Other Identifiers

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5913

Identifier Type: -

Identifier Source: org_study_id