The Return-to-Work Experience of Cancer Patients: A Descriptive Phenomenological Study (NCT07551453) | Clinical Trial Compass
CompletedNot Applicable
The Return-to-Work Experience of Cancer Patients: A Descriptive Phenomenological Study
Italy20 participantsStarted 2024-10-17
Plain-language summary
This study explores the phenomenon of returning to work among individuals affected by cancer, with the objective of providing a description of their lived experience. The ultimate goal is to understand the significance attributed to work, describing the extent to which it is perceived as a protective factor instrumental in restoring a sense of 'normality' and improving quality of life.
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Age: 18 years of age or older.
* Diagnosis: Primary diagnosis of neoplasm.
* Treatment: Currently undergoing at least one anticancer treatment (pharmacological/systemic therapy, surgery, or radiotherapy).
* Setting: Patients managed in a Day Hospital or outpatient setting.
* Employment Status: Engaged in paid and continuous professional activity at the time of diagnosis.
* Language: Ability to understand and speak the Italian language fluently.
* Informed Consent: Ability to provide written informed consent for study participation and data processing (privacy) in accordance with local regulations.
Exclusion Criteria:
* Pre-existing Unemployment: Individuals who were not employed prior to the onset of the disease.
* Psychiatric or Cognitive Impairment: Current diagnosis of psychiatric disorders or cognitive dysfunction that may interfere with the ability to participate in the interview.
* Terminal Prognosis: Patients with a diagnosis of terminal illness or end-of-life status.
* Lack of Voluntary Consent: Individuals who voluntarily choose not to participate in the project or withdraw consent.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Perception of Work Experience and Unmet Health Needs