Ignite Creation Date:
2024-10-26 @ 3:36 PM
Last Modification Date:
2024-10-26 @ 3:36 PM
Study NCT ID:
NCT06537544
Status:
RECRUITING
Last Update Posted:
None
First Post:
2024-07-27
Brief Title:
Comparison of Comprehensive Rehab Program and Pelvic Floor Training in Women With Stress Urinary Incontinence
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Comparison of Comprehensive Rehabilitation Program and Conventional Pelvic Floor Training in Women With Stress Urinary Incontinence
Status:
RECRUITING
Status Verified Date:
2024-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The goal of this clinical trial is to compare a comprehensive rehabilitation program and a conventional pelvic floor training program in women with stress urinary incontinenceto compare the effects of comprehensive rehabilitation program and conventional pelvic floor training on the severity of SUI on the strength of pelvic floor muscle and on quality of life in women with SUI Following the randomization into either the conventional pelvic floor training or comprehensive rehabilitation program group participants will receive their assigned interventions of three weekly sessions for eight weeks
Detailed Description:
The proposed study comparing the effects of conventional pelvic floor training versus a comprehensive rehabilitation program on stress urinary incontinence SUI among perimenopausal women holds significant rationale and importance Given the prevalence and impact of SUI on the quality of life of perimenopausal women investigating the comparative efficacy of these interventions is crucial for informing evidence-based clinical practice The study aims to provide insights into the most effective management strategies for SUI in this population potentially leading to improved treatment outcomes enhanced quality of life and reduced healthcare burden associated with this common condition By addressing this research gap the study has the potential to significantly benefit both individual patients and the broader healthcare system
This will be a randomized controlled trial Non probability sampling technique will be usedThe data collection procedure begins with the recruitment phase potential participants meeting the studys criteria will be identified and provided with detailed information about the research aims and procedures Once recruited participants will undergo a screening process to confirm their eligibility including assessments such as medical history reviews and diagnostic tests After obtaining informed consent baseline assessments will be conducted to establish the participants initial status regarding urinary symptoms and quality of life Following randomization into either the conventional pelvic floor training or comprehensive rehabilitation program group participants will receive their assigned interventions of three weekly sessions for eight weeks
This will be a randomized controlled trial Non probability sampling technique will be usedThe data collection procedure begins with the recruitment phase potential participants meeting the studys criteria will be identified and provided with detailed information about the research aims and procedures Once recruited participants will undergo a screening process to confirm their eligibility including assessments such as medical history reviews and diagnostic tests After obtaining informed consent baseline assessments will be conducted to establish the participants initial status regarding urinary symptoms and quality of life Following randomization into either the conventional pelvic floor training or comprehensive rehabilitation program group participants will receive their assigned interventions of three weekly sessions for eight weeks
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None