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Urinary Incontinence clinical trials

View clinical trials related to Urinary Incontinence.

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NCT ID: NCT04036604 Completed - Quality of Life Clinical Trials

Investigation of The Effect of Pelvic Floor Exercise Programme in Elderly.

Start date: January 21, 2019
Phase: N/A
Study type: Interventional

Alteration of hormonal structure and decreasing of muscle tissue with aging causes pelvic floor dysfunction. Over age of 65 so many factors such as decrease in volume of muscle tissue, decrease in the amount of estrogen / testosterone, and low level of physical activity cause problems such as incontinence, prolapse, constipation and sexual dysfunction The aim of this study is to investigate the effectiveness of pelvic floor exercise program on sexual dysfunction, incontinence, quality of life and physical activity level in elderly.

NCT ID: NCT04031807 Completed - Clinical trials for Stress Urinary Incontinence

Risk Factors for Failure After Single-incision Sling Procedure in Women With Stress Urinary Incontinence

Start date: March 1, 2019
Phase:
Study type: Observational

The main risk factors for failure after single-incision slings are reduced urethral mobility and stress urinary incontinence severity in long-term follow-up.

NCT ID: NCT04029168 Completed - Clinical trials for Pelvic Organ Prolapse

Pelvic Floor Muscles and Success in the Surgical Treatment of Stress Urinary Incontinence and Pelvic Organ Prolapse

Start date: August 1, 2019
Phase:
Study type: Observational

The aim of the study is evaluation of the efficiency of pelvic floor muscles in the context of surgical outcomes in the treatment of stress urinary incontinence and pelvic organ prolapse.

NCT ID: NCT04024085 Completed - Multiple Sclerosis Clinical Trials

Time to be Ready to Void: a New Tool to Assess the Time Needed to Perform Micturition in Multiple Sclerosis

Start date: March 13, 2019
Phase:
Study type: Observational

The aim of the study is to create a specific test to assess the global time required to go to the toilet and to perform micturition, at the moment the patient decides to urinate in multiple sclerosis population, and to assess its reliability.

NCT ID: NCT04008654 Completed - Clinical trials for Urinary Incontinence

Evaluation of the Benefits of Enhanced Recovery After Surgery (ERAS) Protocol in Pelvic Prolapse

Start date: July 5, 2019
Phase: N/A
Study type: Interventional

ERAS protocols have been shown to improve recovery in terms of reduced pain, shortened time to ambulation and length of hospital stay. This study aims to investigate the impact of ERAS protocol on time to mobilization and length of hospital stay in patients undergoing surgery for urinary incontinence and pelvic prolapse.

NCT ID: NCT03988569 Completed - Clinical trials for Pelvic Organ Prolapse

Enhanced Consent and Preparedness for Surgery Trial

ECAPS
Start date: July 1, 2019
Phase: N/A
Study type: Interventional

To develop an audiovisual decision aid (AVDA) to improve the informed consent process. The investigators aim to examine the impact of a comprehensible AVDA that is written below the 8th grade reading level. The AVDA would be used for surgical consent compared to traditional verbal consent. Additionally, the investigators plan to determine whether this effect varies across the measured levels of health literacy of our patients.

NCT ID: NCT03986411 Completed - Clinical trials for Urinary Incontinence

Physiotherapy to Treat Urinary Incontinence in Athletes

POsITIve
Start date: August 27, 2019
Phase: N/A
Study type: Interventional

Nearly half of all adult women suffer with Urinary incontinence (UI), this is more common in athletes. UI is considered to be due to weak pelvic floor muscles. Standard advice encourages strength and endurance training; however, assessment of pelvic floor muscles can sometimes reveal overactive or tight tissues. Evidence suggests athletes have stronger pelvic floors than non-athletes. If the pelvic floor is overactive, general advice regarding pelvic floor strengthening will not improve UI, and may make it worse. This study will explore the feasibility of conducting a larger trial to identify cost effectiveness and benefits of treating athletes with physiotherapy and how this might differ from current practice. 15 -20 athletic women will complete questionnaires regarding their UI and its effects on them. They will receive physiotherapy; the assessment will include a history and internal examination of their pelvic floor. This will inform a tailored rehabilitation program. Interviews will be conducted with some of these women to explore their response to the intervention. Interviews with health professionals will establish current practice for this patient group. The results will tell us how likely it is for athletes to volunteer and take part in a future study and which outcomes are useful.

NCT ID: NCT03985345 Completed - Clinical trials for Stress Urinary Incontinence

Prospective Evaluation of the Connected EMY Biofeedback Probe in the Management of Stress Urinary Incontinence.

Reduc@home
Start date: September 2, 2019
Phase: N/A
Study type: Interventional

After birth, the perineum has to be trained in order to recover its functions. This study is designed to assess the quality of life evolution with the EMY connected device. The secondary purposes are to evaluate patient compliance to the EMY probe, to observe the evolution of urine scores over the duration of the trial in order to consider a comparative study thereafter, and to evaluate the interest of using the EMY connected perineal probe in the context of stress urinary incontinence.

NCT ID: NCT03978741 Completed - Clinical trials for Urinary Incontinence

Study Evaluating the Efficacy and Safety of Yoni.Fit in Women With Stress Urinary Incontinence

Start date: January 3, 2020
Phase: N/A
Study type: Interventional

Study to evaluate the safety and effectiveness of Yoni.Fit for the temporary management of stress urinary incontinence (SUI) in women.

NCT ID: NCT03976414 Completed - Clinical trials for Incontinence, Urinary

Mind Over Matter: Electronic Bladder and Bowel Continence Self-management Program

Start date: June 1, 2019
Phase:
Study type: Observational

The objective of this study is to (1) use participatory ergonomics to adapt and in-person 3-session intervention: Mind Over Matter: Healthy Bowels, Healthy Bladder (MOM) to an electronic program (eMOM), and to (2) compare and characterize eMOM's reach when marketed via community agencies versus Facebook advertising and to collect qualitative and quantitative data about effectiveness and uptake of key behaviors using electronic surveys and phone interviews. The study will also collect information from community agencies that might implement eMOM about its perceived value and their willingness and capacity to implement such a program.