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

Sponsor
Chinese University of Hong Kong (Other)
Overall Status
Recruiting
CT.gov ID
NCT05785286
Collaborator
(none)
66
2
13.1
33
2.5

Study Details

Study Description

Brief Summary

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

Condition or Disease Intervention/Treatment Phase
  • Other: BPH 3-item questionnaire

Detailed 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.

Study Design

Study Type:
Observational
Anticipated Enrollment :
66 participants
Observational Model:
Other
Time Perspective:
Prospective
Official Title:
To Linguistically and Psychometrically Validate the Hong Kong Chinese Version of the BPH 3-item Questionnaire.
Actual Study Start Date :
Feb 27, 2023
Anticipated Primary Completion Date :
Jan 31, 2024
Anticipated Study Completion Date :
Mar 31, 2024

Arms and Interventions

Arm Intervention/Treatment
Subject with male LUTS

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.

Other: BPH 3-item questionnaire
BPH 3-item questionnaire. 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).

Subject who is waiting for their transurethral ablative prostate surgery

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.

Other: BPH 3-item questionnaire
BPH 3-item questionnaire. 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).

Outcome Measures

Primary Outcome Measures

  1. Reliability of BPH 3-item questionnaire [up to 24 weeks]

    Reliability was assessed by internal consistency and test-retest correlation. (ρ) correlation, with the IPSS (total score / voiding domain (ie Q.1, 3, 5, 6) and prostate volume measured by TRUS.

  2. Internal consistency of BPH 3-item questionnaire [up to 24 weeks]

    Internal consistency was assessed by Cronbach's alpha coefficients, with >0.7 being considered acceptable

  3. Test-retest reliability of BPH 3-item questionnaire [up to 24 weeks]

    Test-retest reliability was assessed by intra-class correlation coefficient. Values between 0.6 and 0.8 indicate substantial agreement, and values over 0.8 indicate near-perfect agreement

  4. The convergent validity of the BPH 3-item questionnaire [up to 24 weeks]

    was estimated by Spearman rho (ρ) correlation, with the IPSS (total score / voiding domain (ie Q.1, 3, 5, 6) and prostate volume measured by TRUS.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 90 Years
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
No
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Alice Ho Miu Ling Nethersole Hospital Hong Kong Hong Kong
2 Prince of Wales Hospital Sha Tin Hong Kong

Sponsors and Collaborators

  • Chinese University of Hong Kong

Investigators

  • Principal Investigator: Chi Fai NG, MD, Chinese University of Hong Kong

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Chi Fai NG, Professor, Chinese University of Hong Kong
ClinicalTrials.gov Identifier:
NCT05785286
Other Study ID Numbers:
  • CRE-2022.645
First Posted:
Mar 27, 2023
Last Update Posted:
Mar 27, 2023
Last Verified:
Mar 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 27, 2023