Anxiety in Patients Under Active Surveillance for Localized Prostate Cancer and Their Partners.
Recruiting now
Conditions studied: Prostate Cancer
In brief
Prostate cancer (PCa) is the most common cancer and the third leading cause of cancer-related death among men in France. Active surveillance is one of the management options for low-risk prostate cancer. Its aim is to delay or avoid radical treatment, such as surgery or radiotherapy, which can cause side effects including urinary incontinence, erectile dysfunction, or radiation-induced cystitis. Active surveillance involves regular monitoring of potential tumor progression through serum PSA testing, MRI scans, and prostate biopsies. Few studies have investigated the psychological adjustment of patients undergoing active surveillance for prostate cancer, and even fewer have explored the relationship between the patients' anxiety symptoms and those of their partners. To our knowledge, no study has yet quantitatively or qualitatively assessed the anxiety of both patients and their partners. It appears essential to better characterize the anxiety symptoms in these individuals in order to offer them appropriate psychological support.
Key facts
- Study ID
- NCT07351461
- Run by
- University Hospital, Lille
- People needed
- 432
- Starts
- 2025-03-23
- Expected to finish
- 2027-03-23
- Last updated by the study team
- 2026-01-20
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Age ≥ 18 years.
- Patients who started active surveillance for localized prostate cancer from 2007 to 2023 and are followed in the Urology Department of Lille University Hospital.
- Affiliation to a social security scheme.
- Obtaining patient consent.
- Having a life partner or an unidentified partner recognized as the person sharing the patient's daily life
You may not qualify if…
- Lack of proficiency in the French language.
- Minor patients, those under legal protection measures, or deprived of liberty.
- Lack of medical insurance coverage.
- Patients refusing to participate in the study.
Where it is running
- CHU de Lille — Lille, France (enrolling)
Full record on ClinicalTrials.gov
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