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Effect of Visceral vs Total Body Fat Reduction in Obese Female With Stress Urinary Incontinence

Effect of Visceral vs Total Body Fat Reduction in Obese Female With Stress Urinary Incontinence by EMG and Iciq Questionnaire

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05944484
Enrollment
60
Registered
2023-07-13
Start date
2020-11-30
Completion date
2023-06-05
Last updated
2023-07-13

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

Conditions

Stress Urinary Incontinence

Keywords

Visceral fat, total body fat, obese female, stress urinary incontinence

Brief summary

The aim of this study is to investigate the visceral fat reduction versus total body fat reduction on stress urinary incontinence in obese females.

Detailed description

compare the effect of visceral fat reduction versus total body fat reduction on stress urinary incontinence in obese females. control group: consist of 20 obese women. They will receive Kegel exercises only 3 session/ week for 12 weeks. Diet group: consist of 20 obese women. They will receive low caloric diet and Kegel exercises 3 session/week for 12 weeks. Ultrasound cavitation group: consist of 20 obese women. They will receive Kegel exercises 3 session/week and ultrasound cavitation two sessions per week.

Interventions

BEHAVIORALlow caloric diet, ultrasound cavitation,Kegel exercises

* low caloric diet (800-1200) calories/day,). According to each patient, diet contained (carbohydrate protein, fats, minerals, vitamins). 50 to 55% of total calories are carbohydrates, 10 to 15% of total calories protein. Fat limited to less than about 28% of daily total calories .Women took 1200 calories in the first month, 1000 calories in the second month, and 800 calories in the third month. Every week, each woman allowed to change the types of food to avoid boarding. * ultrasound cavitation emits low-frequency ultrasound 40 khz for 30 minutes on abdomen twice/ week with 3 days apart for 12 weeks. kegel exercise: Each woman in the study took the same Kegel exercise program performed the Kegel exercise for 12 weeks (3 sessions per week)

Sponsors

Dina Mohamed Tarek Mansour El-kasrawy
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Masking description

Double (participant,outcomes Assessor) Random generator

Intervention model description

Visceral fat reduction vs total body fat reduction on obese female with stress urinary incontinence

Eligibility

Sex/Gender
FEMALE
Age
35 Years to 48 Years
Healthy volunteers
No

Inclusion criteria

* They will be diagnosed with stress urinary incontinence grade≥ 1 * Their age will range from 35-48 years old. * Their body mass index will exceed 29.9 kg/m². * Their hip waist ratio will be more than 0.85 cm. * They will be multipara \>1.

Exclusion criteria

* · Fecal incontinence, urge incontinence, overflow incontinence or functional incontinence or prolapse. * Diabetes, asthma, cardiovascular, or renal diseases * Taking medication for stress urinary incontinence or hormonal replacement therapy. * Gynecological surgeries, or surgeries for obesity. * Pregnant women.

Design outcomes

Primary

MeasureTime frameDescription
stress urinary incontinence12 weeksevaluate stress urinary incontinence by The International Consultation on Incontinence Questionnaire ranged from (0-21) Question items: Frequency or urinary incontinence Amount of leakage Overall impact of urinary incontinence Self-diagnostic item. The ICIQ-UI Short form provides a score ranging from 0-21. With a higher score indicating greater severity of symptoms. The self-diagnostic portion of the questionnaire is not given a score

Secondary

MeasureTime frameDescription
waist circumference12 weeksmeasure waist circumference in centimeter
Measure weight12 weeksMeasure weight in kilogram
Measure body mass index12 weeksweight and height will be combined to report BMI in kg/m\^2

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026