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To Linguistically and Psychometrically Validate the Hong Kong Chinese Version of the BPH 3-item Questionnaire

The Chinese University of Hong Kong logo

The Chinese University of Hong Kong

Status

Completed

Conditions

Benign Prostatic Hyperplasia (BPH)

Treatments

Other: BPH 3-item questionnaire

Study type

Observational

Funder types

Other

Identifiers

NCT05785286
CRE-2022.645

Details and patient eligibility

About

This study is to linguistically and psychometrically validate the translated and culturally adapted Hong Kong Chinese version of the BPH 3-item questionnaire.

Full description

A new BPH 3-item questionnaire has recently been developed and published, and it may serve as a screening tool for male-LUTS due to symptomatic BPE. The questionnaire consists of only three items. A raw score ranging from 0 to 5 is assigned to each of the items, giving a final total score varying from 0 (no symptom) to 15 (very symptomatic). This questionnaire has been translated and validated into five different European languages and was harmonized cross-culturally for linguistic validation, followed by psychometric accuracy testing.

This new questionnaire may help rationalize more early commencement of therapy aimed at reducing the prostate size for the treatment of male LUTS due to BPE.

Enrollment

66 patients

Sex

Male

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18 - 90 years old Chinese male subjects presented with male-LUTS for at least 4 weeks
  • The subjects are able to read and fully comprehend with the content of the questionnaires
  • The subjects are willing to give informed consent for the study

Exclusion criteria

  • peak uroflow ≤4mL/sec;
  • post-void residual (PVR) ≥300 mL;
  • unable to give informed consent
  • need of clean intermittent self-catheterization / indwelling urethral catheterization at the time of enrolment;
  • Surgical treatment (e.g. TURP) of bladder outlet obstruction / symptomatic benign prostate enlargement (BPE) ≤ 3 months before entry into the study
  • clinical suspicion / presence of untreated urethral stricture and/or bladder neck stenosis,
  • clinical suspicion / presence of genitourinary cancer including active prostate cancer with ongoing surgical or radiation treatment, or the need of treatment, or bladder cancer, or persistent unexplained hematuria;
  • uncontrolled heart failure / diabetes mellitus(DM) / hypertension(HT);
  • neuropathic bladder;
  • Currently on dialysis or in consideration for dialysis due to end stage renal disease;
  • More than 3 urinary tract infections within the last 12 months;
  • Unstable dose of diuretic within the past 3 months;
  • Has an artificial urinary sphincter;
  • Impaired mental status;
  • male-LUTS due to urinary tract infections / chronic prostatitis / chronic pelvic pain

Trial design

66 participants in 2 patient groups

Subject with male LUTS
Description:
Male subjects who have been bothered by male LUTS for at least 4 weeks and are still able to pass urine on their own without the need of assistance or urethral catheterization.
Treatment:
Other: BPH 3-item questionnaire
Subject who is waiting for their transurethral ablative prostate surgery
Description:
Male subjects who are waiting for BPH surgery and are still able to pass urine on their own without the need of assistance or urethral catheterization.
Treatment:
Other: BPH 3-item questionnaire

Trial contacts and locations

2

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Central trial contact

Chi Fai NG, MD

Data sourced from clinicaltrials.gov

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