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Pelvic Floor Muscle Training and Biofeedback or Standard Therapy in Men Who Have Undergone Radical Prostatectomy or Transurethral Resection of the Prostate

Phase 3CompletedNCT00632138
Aberdeen Royal Infirmary800 enrolled

Overview

RATIONALE: Personalized training by a health professional may improve urinary incontinence. It is not yet known whether pelvic floor muscle training and biofeedback are more effective than standard therapy in improving urinary continence after radical prostatectomy or transurethral resection of the prostate. PURPOSE: This randomized phase III trial is studying pelvic floor muscle training and biofeedback to see how well it works compared with standard therapy in men who have undergone radical prostatectomy or transurethral resection.

OBJECTIVES: * To establish whether conservative physical treatment delivered personally by a trained health professional results in better urinary and other outcomes compared with standard management in men who are incontinence after prostate surgery. OUTLINE: This is a multicenter study. Patients are stratified according to type of operation (radical prostatectomy vs transurethral resection of prostate). Patients are randomized to 1 of 2 treatment arms. * Arm I (intervention group): At 6 weeks after surgery, patients undergo an assessment of their symptoms by a physiotherapist or continence nurse. All patients are taught pelvic floor muscle training and men with urgency or urge incontinence are also taught bladder training. Pelvic floor training consists of 3 maximum pelvic floor contractions in 3 positions (standing, sitting, and lying down) twice a day, lifting of the pelvic floor while walking, tightening of the pelvic muscles before activities, and tightening of the pelvic muscles after urinating to squeeze out any last drops. The strength of the pelvic floor contractions is monitored by biofeedback involving digital anal assessment and relaying the information back to men in order that they know when they are performing contractions correctly and to inform them when they are increasing the strength or duration of their contractions. Therapists may use machine-mediated biofeedback with an anal biofeedback probe at their discretion in addition to digital anal assessment. Bladder training consists of gradually delaying urination by pelvic floor muscle contraction and distracting activities to teach the bladder to hold increasing volumes of urine. Patients also receive a customized Pelvic Floor Exercise Booklet describing pelvic floor muscle training in addition to a customized Lifestyle Advice Booklet giving general lifestyle advice. Patients have reinforcement sessions at approximately 2, 6, and 12 weeks after the first appointment. * Arm II (control group): Patients receive a customized Lifestyle Advice Booklet containing supportive lifestyle advice only (without reference to pelvic floor muscle training) by mail following randomization. Patients do not receive formal assessment or treatment but will be able to access usual care and routine NHS services if they feel they need help, including written advice if this is part of routine hospital care. All patients keep a urinary diary at 3, 6, 9, and 12 months that includes frequency of urination (day and night), daily episodes of incontinence and quantity of loss, daily use of pads, and the need to change clothing or bedding. A Health Care Utilization Questionnaire will be obtained at 3 and 9 months. Additional questionnaires are obtained at baseline and 6 and 12 months. The use of NHS services, pads, and practice of pelvic floor muscle training is documented in both groups using information from questionnaires and Urinary Diaries. Six months after the last patient has been recruited, a check for Scottish men only is performed to compare self-reported operations, diagnoses, and hospital admissions with centrally collected data to validate a proportion of the data. After completion of study treatment, patients are followed at 6 and 12 months.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

SUPPORTIVE_CARE

Enrollment

800

Conditions

Nonmalignant NeoplasmProstate CancerPsychosocial Effects of Cancer and Its TreatmentSexual DysfunctionUrinary Incontinence

Interventions

exercise interventionBEHAVIORAL
questionnaire administrationOTHER
biofeedbackPROCEDURE
management of therapy complicationsPROCEDURE
psychosocial assessment and carePROCEDURE
quality-of-life assessmentPROCEDURE

Eligibility

Sex: MALE
Medical Language ↔ Plain English
DISEASE CHARACTERISTICS: * Men who have undergone a radical prostatectomy for prostate cancer or men who have undergone a transurethral resection of the prostate for benign prostatic hypertrophy * Urinary incontinence at six weeks after prostate surgery * Incontinence is defined as a response on the screening questionnaire indicating a loss of urine including how often and how much PATIENT CHARACTERISTICS: * Able to comply with intervention * Able to complete study questionnaires PRIOR CONCURRENT THERAPY: * See Disease Characteristics * No referral for formal therapy (teaching of pelvic floor muscle training) due to prostate surgery * No concurrent or planned radiotherapy during the first 3 months after surgery * No palliative endoscopic resection of prostate due to outflow obstruction for advanced prostate cancer

Locations (37)

Tameside General Hospital

Ashton-under-Lyne, England, United Kingdom

Southmead Hospital

Bristol, England, United Kingdom

Bristol Royal Infirmary

Bristol, England, United Kingdom

Mid Cheshire Hospitals Trust- Leighton Hopsital

Crewe, England, United Kingdom

Royal Bolton Hospital

Farnworth, England, United Kingdom

King George Hospital

Ilford, Essex, England, United Kingdom

Ipswich Hospital

Ipswich, England, United Kingdom

Airedale General Hospital

Keighley, England, United Kingdom

Leeds Cancer Centre at St. James's University Hospital

Leeds, England, United Kingdom

St. Mary's Hospital

London, England, United Kingdom

...and 27 more locations

Outcomes

Primary Outcomes

Subjective report of urinary continence at 12 months

Incremental cost per quality-adjusted year

Secondary Outcomes

Subjective report of continence or improvement of urinary incontinence at 3, 6, and 9 months after randomization and improvement at 12 months

Objective report of the number of incontinent episodes in the previous week from the urinary diary

Duration of incontinence based on time of resolution relative to time of operation and randomization

Use of absorbent pads, penile collecting sheath, bladder catheter, or bed/chair pads

Number and type of incontinence products used

Co-existence, cure or development of urgency, or urge incontinence

Urinary frequency

Nocturia

Fecal incontinence (passive or urge)

Other bowel dysfunction (i.e., urgency, constipation, or other bowel diseases)

Sexual function at 12 months including information about erection, ejaculation, retrograde ejaculation, pain, change in sex life, and reason for change

Incontinence-specific quality of life outcome measure using the 10-point scale and ICI questionnaire

General health measures

Need for alternative management for incontinence (e.g., surgery or drugs)

Use of GP, nurse, consultant urologist, or physiotherapist

Visits to GP

Visits to practice nurse

Use of pelvic floor muscle training

Lifestyle changes (i.e., weight, constipation, lifting, coughing, or exercise)

Patient costs (e.g., self care [e.g., pads or laundry], travel to health services, or sick leave)

Cost of conservative trial treatment

Cost of alternative or additional NHS treatments (e.g., pads, catheters, drugs [e.g., adrenergic agonists, anticholinergics, or oral medication for erectile dysfunction], hospital admissions, or further surgery)

Other measures of cost-effectiveness (e.g., incremental cost per additional man continent at 12 months)

Data from ClinicalTrials.gov

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