Exploring the unmet needs of cancer survivors in Reggio Emilia

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

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.

Why it matters

Who can join: the full rules

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 it's running

• 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

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.