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The Return-to-Work Experience of Cancer Patients: A Descriptive Phenomenological Study

The Return-to-Work Experience of Cancer Patients: A Descriptive Phenomenological Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07551453
Acronym
REWORK
Enrollment
20
Registered
2026-04-24
Start date
2024-10-17
Completion date
2025-09-30
Last updated
2026-04-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer

Brief 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.

Detailed description

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.

Interventions

None listed

Sponsors

Centro di Riferimento Oncologico - Aviano
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Perception of Work Experience and Unmet Health Needsup to 1 yearA qualitative assessment of how cancer patients perceive their professional life during treatment will be carried out using Colaizzi framework (1978). The study uses semi-structured interviews to identify "unexpressed health needs"-specific physical, psychological, or organizational requirements related to working while undergoing therapy that are not currently addressed by standard care.

Secondary

MeasureTime frameDescription
Identification of Potential Nursing Interventions for Work-Related Supportup to 1 yearAnalysis of patient interviews using a qualitative approach to categorize and define specific nursing actions that can address the work-related health needs identified in the primary objective.

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 25, 2026