Exploring the unmet needs of cancer survivors in Reggio Emilia
The Unmet Needs of Cancer Survivors in Ausl IRCCS Reggio Emilia Reality: a Qualitative Study and Framework Analysis
This study is trying to find out what cancer survivors need most after finishing their treatment to help improve their care and quality of life.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 45 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University of Modena and Reggio Emilia Academic / other |
| Locations | 1 site (Reggio Emilia, Reggio Emilia) |
| Trial ID | NCT06236373 on ClinicalTrials.gov |
What this trial studies
This observational study aims to investigate the unmet needs of cancer survivors who have recently completed the acute phase of treatment for various cancers, including breast, prostate, thyroid, and colorectal cancers. By utilizing qualitative methods such as focus groups and interviews, the study seeks to gather insights from patients, caregivers, and stakeholders to enhance aftercare services. The goal is to identify gaps in care and improve the overall quality of life for cancer survivors by addressing their specific challenges and needs.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18 and over who have completed the acute phase of treatment for breast, prostate, thyroid, colorectal, or multiple myeloma cancers.
Not a fit: Patients who do not speak or understand Italian or those with significant cognitive impairments may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved aftercare services that better meet the needs of cancer survivors, enhancing their quality of life.
How similar studies have performed: Other studies have successfully explored unmet needs in cancer survivorship, indicating that this approach is both relevant and necessary.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adult aged18 years or over. * Individuals who have a history of breast, prostate, thyroid, colorectal, multiple myeloma or lymphoma cancer within the past years who have completed the acute phase of treatment, and are in follow-up or are receiving maintenance treatment; * Caregivers for an individual who meets the above criteria, who are aged 18 years or over. * Stakeholders for individual who meets the above criteria, who are aged 18 years or over. Exclusion Criteria: * Individuals who do not wish to participate * Individuals who do not understand and/or speak Italian * Individuals with significant cognitive impairment, learning difficulty, or communication difficulty such that understanding the nature of the study, the interview questions, or participating in a focus group or an on-line or in-presence interview would not be practical.
Where this trial is running
Reggio Emilia, Reggio Emilia
- Casa della Salute ex Spallanzani — Reggio Emilia, Reggio Emilia, Italy (Recruiting)
Study contacts
- Principal investigator: Stefania Costi, PhD — Physical Medicine and Rehabilitation Unit, Azienda Unità Sanitaria Locale - IRCCS di Reggio Emilia
- Study coordinator: Angela Contri, MA
- Email: angela.contri@unimore.it
- Phone: +393478824741
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.