Comparison the Effect of Pelvic Floor Muscle Biofeedback prior or post Radical Prostatectomy on Urinary Incontinence

Comparison the Effect of Pelvic Floor Muscle Biofeedback prior or post Radical Prostatectomy on Urinary Incontinence: A Randomized Clinical Trial

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20200429047243N1

Enrollment

Registered

2020-05-05

Start date

2019-09-23

Completion date

Unknown

Last updated

2020-05-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neuromuscular dysfunction of bladder, unspecified. Neuromuscular dysfunction of bladder, unspecified , prostate cancer

Interventions

Intervention 1: Intervention group: biofeedback prior to radical prostatectomy. Intervention 2: Intervention group: biofeedback after radical prostatectomy. Intervention 3: Control group: no biofeedba

Eligibility

Sex/Gender

Male

Inclusion criteria

Inclusion criteria: Men with prostate cancer confirmed with TRUSBx who are candidates for radical prostatectomy

Exclusion criteria

Exclusion criteria: patients who were diagnosed with prostate cancer following Transurethral Resection of Prostate patients who received pelvic radiotherapy regardless of their primary malignancy spinal cord injury comorbidities that can affect urinary continence (such as: diabetes mellitus, overactive bladder, urethral stricture, etc.) history of pelvic or retroperitoneal surgery neurologic disorders (e.g.: Multiple Sclerosis, seizures, etc.)

Design outcomes

Primary

Measure	Time frame
Biofeedback before radical prostatectomy on urinary incontinence after surgery according to King's Health Questionnaire. Timepoint: before surgery and 1,3 and 6 months after surgery. Method of measurement: King's Health Questionnaire.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSaeed Montazeri

Shahid Beheshti University of Medical Sciences

saeed.montazeri89@gmail.com+98 21 2271 8006

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026