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Completed

NCT Number: NCT06599190

Effect Of Abdominal Hypopressive Training On Stress Urinary Incontinence

Fifty female athletes suffering from stress incontinence (SUI) will participate in this study. They will be selected from El Zohour Club, New Cairo City.

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Key information

About this study

They will be randomly distributed into 2 groups equal in numbers:

Group (A) (Control group) consists of 25 female athletes. They will receive nutritional instructions and pelvic floor muscle exercises three sessions/week for 3 months.

Group (B) (Study group) consists of 25 female athletes. They will receive the same treatment for the control group and abdominal hypopressive exercises three sessions/week of 30 mins per week for 3 months.

Before data collection, the purpose and procedures will be fully explained to the females. Informed consent will be obtained from each female. Each female will be evaluated following a standard protocol.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Female athletes suffering from SUI.
  • They will be diagnosed with SUI using bladder stress test.
  • Their ages will range from 14-18 years old.
  • Their body mass index (BMI) will range from 18.5-24.9 kg/m2.
  • They are single females.

Exclusion criteria

The female athlete will be excluded if they had:

  • Urinary tract infection.
  • Family history of genito-urinary tract cancer.
  • Diabetes mellitus.

Treatment and study plan

pelvic floor exercises, nutritional instructions

Other

They will receive nutritional instructions and pelvic floor muscle exercises three sessions/week for 3 months.

abdominal hypopressive exercises, pelvic floor exercises, nutritional instructions

Other

consists of 25 female athletes. They will receive the same treatment for the control group and abdominal hypopressive exercises three sessions/week of 30 mins per week for 3 months.

Primary outcomes

  1. Assessment of urine loss

    Time frame: 24 hours pad test for12 weeks

    Pad testing will be used to quantify the volume of urine loss by weighing an absorbent pad before and after some type of leakage provocation. The test will start with weighting clean empty pad in grams. Then, it will be used until next time and weighted again. The weight of the used pad will be subtracted from the weight of the empty pad so the net result will determine the amount of leakage.

  2. assesment of pelvic floor muscle contraction and tonning

    Time frame: 12 weeks

    The measurements will be taken in crock-lying position with a full bladder, neutral lumbar spine. The ultrasound transducer will be inserted transversely directly superior to the symphysis pubis, probe is tilted 60 degrees from vertical (Arab, 2010). Every female will perform 3 maximal PFM contractions so that displacement of the bladder wall, because of a PFM contraction, could be measured.

Secondary outcomes

  1. Assessment of symptoms and health related quality of life

    Time frame: 12 weeks

    The ICIQ-SF will be used in assessment of each female in both groups. It is used to measure severity and impact of UI on the quality of life in women. The ICIQ-SF is formed of six items of which four main items ask for rating of UI symptoms in the past 4 weeks. A score of zero means no leakage of urine and no affection on quality of life. (Question 1): quantifies the frequency of urinary leaking, (question 2): evaluates the amount of leaking and (question 3): how much the urinary incontinence interferes with everyday life (Hilton and Robinson, 2011). The scores for items 3, 4 and 5 are taken for the final ICIQ-SF score. Items 1 and 2 are demographic and the final item is a self-diagnostic item for the type of UI. ICIQ- SF (range 0-21) is given four scoring categories: slight (1-5), moderate (6-12), severe (13-18) and very severe (19-21).

Sponsors and collaborators

Lead sponsor

Badr University

Other

Collaborators

  • Cairo University

Registry information

Official study title

Effect Of Abdominal Hypopressive Training On Stress Urinary IncontinenceIn Female Athletes

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
Sep 19, 2024
Registry last updated
Mar 6, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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