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Spots Global Cancer Trial Database for Pelvic Floor Muscle Training and Biofeedback or Standard Therapy in Men Who Have Undergone Radical Prostatectomy or Transurethral Resection of the Prostate

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Trial Identification

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

Official Title: MAPS (Men After Prostate Surgery) : Conservative Treatment for Men With Urinary Incontinence After Prostate Surgery; Multicentre Randomised Controlled Trial of Pelvic Floor Muscle Training and Biofeedback [MAPS]

Study ID: NCT00632138

Study Description

Brief Summary: 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.

Detailed Description: 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.

Eligibility

Minimum Age:

Eligible Ages: CHILD, ADULT, OLDER_ADULT

Sex: MALE

Healthy Volunteers: No

Locations

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

Macclesfield District General Hospital, Macclesfield, England, United Kingdom

James Cook University Hospital, Middlesbrough, England, United Kingdom

Freeman Hospital, Newcastle-Upon-Tyne, England, United Kingdom

Norfolk and Norwich University Hospital, Norwich, England, United Kingdom

Nottingham City Hospital, Nottingham, England, United Kingdom

Berkshire Cancer Centre at Royal Berkshire Hospital, Reading, England, United Kingdom

Queens Hospital, Romford, England, United Kingdom

Hope Hospital, Salford, England, United Kingdom

Royal Hallamshire Hospital, Sheffield, England, United Kingdom

Lister Hospital, Stevenage, England, United Kingdom

Stepping Hill Hospital, Stockport, England, United Kingdom

Taunton and Somerset Hospital, Taunton, England, United Kingdom

Hillingdon Hospital, Uxbridge, England, United Kingdom

New Cross Hospital, Wolverhampton, England, United Kingdom

Yeovil District Hospital, Yeovil, England, United Kingdom

Aberdeen Royal Infirmary, Aberdeen, Scotland, United Kingdom

Ayr Hospital, Ayr, Scotland, United Kingdom

Ninewells Hospital, Dundee, Scotland, United Kingdom

Queen Margaret Hospital - Dunfermline, Dunfermline, Scotland, United Kingdom

Edinburgh Cancer Centre at Western General Hospital, Edinburgh, Scotland, United Kingdom

Falkirk and District Royal Infirmary, Falkirk, Scotland, United Kingdom

Southern General Hospital, Glasgow, Scotland, United Kingdom

Inverclyde Royal Hospital, Greenock, Scotland, United Kingdom

Raigmore Hospital, Inverness, Scotland, United Kingdom

Pinderfields General Hospital, Wakefield, Scotland, United Kingdom

Morriston Hospital NHS Trust, West Glamorgen, Scotland, United Kingdom

University Hospital of Wales, Cardiff, Wales, United Kingdom

Contact Details

Name: Cathryn Glazener, MD

Affiliation: Aberdeen Royal Infirmary

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

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