NCT07760688Recruiting
Structured Periprocedural Nursing Interventions in Men Undergoing Transrectal Prostate Biopsy
Impact of Structured Periprocedural Nursing Interventions on Resilience and Anxiety in Men Undergoing Transrectal Prostate Biopsy: A Prospective Longitudinal Interventions Study With Histopathological Stratification
Source: ClinicalTrials.gov · Last updated 12 Aug 2026
Brief summary (registry, in English)
This prospective longitudinal interventional study aims to evaluate the effect of structured peri-procedural nursing interventions on resilience and anxiety in men undergoing transrectal prostate biopsy. Participants will receive a standardized nursing intervention before and after the biopsy procedure. Resilience, anxiety, pain, lower urinary tract symptoms, and perceived nursing support will be assessed at predefined time points. Histopathological findings (benign or malignant) will be used for subgroup analyses. The study is conducted at the University Clinical Hospital Mostar, Bosnia and Herzegovina.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 120 (estimated)
- First submitted
- 7 Aug 2026
- Start date
- 4 Aug 2026
- Primary completion date
- 4 Jul 2027
- Lead sponsor
- University of Mostar
- Diseases
- Prostate cancer
- NCT number
- NCT07760688
What you commit to
- Study type: Interventional
- Planned participants: 120
- From 4 Aug 2026 to the primary completion date, 4 Jul 2027
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Previous disgnosis of prostate cancer.
Other illness
- Severe cognitive impairment or psychiatric disorder preventing questionnaire completion.
Other
- Inabillity to provide informed consent.
- Inabillity to complete follow-up assessments.
- Withdrawal of informed consent at any time.
Who the study is looking for
- Male participants aged 40 years or older.
- Scheduled for transrectal ultrasound-guided prostate biopsy because of suspected prostate cancer.
- Able to understand the study procedures and provide written informed consent.
- Willing to complete all study assessments during the follow-up period.
Age in the registry: 40 years to - · Sex: Male · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| University Clinical Hospital Mostar Coordinator of this site? Confirm its status | Mostar | Bosnia and Herzegovina | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.