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CompletedNCT07448545Updated Mar 5, 2026

Turkish Version of the UCLA Prostate Cancer Index

An observational study in Prostate Cancer (Diagnosis), Quality of Life and Reliability, sponsored by Lokman Hekim University. Completed at 1 site in Turkey (Türkiye). Open to male participants. Per ClinicalTrials.gov, last updated 2026-03-05.

Sponsored by Lokman Hekim University · Observational

Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
115
Sex
Male
01

Study summary

This study will evaluate the cross-cultural adaptation, validity, and reliability of the Turkish version of the UCLA Prostate Cancer Index in men diagnosed with prostate cancer. The original instrument will be translated and culturally adapted following standardized procedures. The psychometric properties of the Turkish version will be examined in patients attending routine follow-up visits at a urology clinic.

Internal consistency will be assessed using Cronbach's alpha coefficients, and test-retest reliability will be evaluated using intraclass correlation coefficients (ICC) in a subset of participants. Measurement error will be determined by calculating the standard error of measurement (SEM) and the smallest real difference at the 95% confidence level (SRD95). Construct validity will be examined through exploratory factor analysis, and convergent validity will be assessed by testing predefined hypotheses regarding correlations between the UCLA Prostate Cancer Index and established quality-of-life instruments (SF-36 and EORTC QLQ-PR25).

The findings are expected to provide a reliable and valid prostate cancer-specific quality-of-life assessment tool for use in Turkish-speaking populations.

02

Conditions studied

  • Prostate Cancer (Diagnosis)
  • Quality of Life
  • Reliability
  • Validity
  • UCLA Prostate Cancer Index
03

In context

Prostatic Neoplasms

6,370 studies on the registry are indexed under Prostatic Neoplasms; 1,400 are open to participants now.

This study's enrollment of 115 is below the median of 200 across 1,181 observational studies indexed under Prostatic Neoplasms.

Browse Prostatic Neoplasms studies →

Lead sponsor

Lokman Hekim University is the lead sponsor of 41 studies on the registry; 16 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
Male
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

The study population consists of men aged 45 years and older who have been diagnosed with prostate cancer and are attending routine follow-up visits at a urology outpatient clinic in Türkiye.

Inclusion criteria

  • Male patients
  • Diagnosis of prostate cancer

Exclusion criteria

Exclusion Criteria:

  • Severe psychiatric or mental disorders that may impair the ability to complete the questionnaires properly
  • Presence of congenital deformities
05

Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
115 participants (actual)
Target follow-up
115 Days
Patient registry
Yes

Groups and cohorts

  • Prostate Cancer Patients

    This cohort will consist of men aged 45 years and older who have been diagnosed with prostate cancer and are attending routine follow-up visits at a urology outpatient clinic

    Other: Questionnaires

Interventions

  • OtherQuestionnaires

    Participants will complete the Turkish version of the UCLA Prostate Cancer Index along with the SF-36 and EORTC QLQ-PR25 questionnaires. No intervention will be applied.

06

What researchers measure

Primary outcomes

  1. UCLA Prostate Cancer Index

    The University of California, Los Angeles (UCLA) Prostate Cancer Index was developed in English in 1998 by Litwin et al. and has been psychometrically validated in prostate cancer populations. It evaluates urinary, sexual, and bowel function and the associated symptom-related bother in men treated for prostate cancer

    Time frame: 1 hour

  2. EORTC QLQ-PR25

    The EORTC QLQ-PR25 is a prostate cancer-specific module consisting of 25 items and comprising six symptom subdomains: urinary symptoms, incontinence aid, bowel symptoms, hormonal treatment-related symptoms, sexual activity, and sexual functioning

    Time frame: 1 hour

  3. SF-36

    It is a widely used 36-item questionnaire that evaluates health-related QoL across eight domains, including physical functioning, role limitations due to physical and emotional problems, mental health, vitality, social functioning, bodily pain, and general health

    Time frame: 1 hour

07

Study locations

1 site
  • Lokman Hekim University, Ankara, Ankara
    Ankara, 6510, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 5, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07448545
Lead sponsor
Lokman Hekim University
Responsible party
Demet Öztürk (Assistant profesor, Lokman Hekim University) — Principal investigator
First posted
Mar 4, 2026
Start date
Jan 20, 2022
Primary completion
Jan 28, 2026
Completion
Jan 28, 2026
Last update
Mar 5, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2026. You cannot join it, but the record below documents what was studied.

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