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Completed

NCT Number: NCT06521008

Effect of Diaphragmatic Training on Urgency Urinary Incontinence in Postmenopausal Women

The purpose of this study was to determine the effect of diaphragmatic training on urgency urinary incontinence in postmenopausal women.

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Key information

About this study

Urgency urinary incontinence affects 9-13% of women, increasing with age and impacting daily activities, quality of life, depression, and social isolation. It is a significant source of dependency among the elderly and a factor in nursing home admissions. Untreated incontinence can lead to falls, infections, and loss of independence. Conservative management is the first-line therapy, but pelvic floor muscle training is a potential treatment method. This study aims to evaluate the effectiveness of diaphragmatic training on urinary incontinence in postmenopausal women.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Postmenopausal women suffer from UUI.
  • They will be multipara more than 1.
  • Their age will range from 55-65 years old.
  • Their body mass index (BMI) will range from 25-29.9 kg/m2..
  • They will experience menopause at least for 3 years.

Exclusion criteria

  • Urinary tract infection
  • Previous surgery for urinary incontinence
  • Upper motor neuron diseases
  • History of genito-urinary cancer
  • Previous pelvic irradiation
  • Pure stress urinary incontinence
  • Genital prolapse
  • Diabetes mellitus
  • Pace maker

Treatment and study plan

anti muscarinic drugs

Drug

a selective anti muscarinic drugs (5-10mg) once per day for 12 weeks.

Instructions including bladder training

Other

The program teaches women skills and strategies to prevent incontinence, including bladder irritants like caffeine and discussing bowel habits to prevent constipation. It also teaches them how to respond adaptively to urgency, such as pause, sit down, relax, and contract pelvic muscles to diminish urgency and prevent urine loss. Once urgency subsides, they can proceed to the toilet at a normal pace. The program emphasizes the importance of educating patients about bladder irritants and bowel habits.

pelvic floor muscle training (PFMT)

Other

The training program teaches bladder control through contracting the striated skeletal pelvic floor muscles (PFM). The women are instructed to empty their bladder, lie in a lithotomy position, and tighten their pelvic floor muscles. The duration of contraction and repetitions is gradually increased, totaling 20-30 minutes. The program is 3 sessions per week under supervision for 12 weeks, and each woman is instructed to perform exercises at home until they can do 300 contractions per day.

abdominal exercise

Other

Women will engage in transverse abdominis exercises, focusing on drawing the lower abdominal wall towards the spine and pressing the lumbar region downward, repeated for 15 minutes per session, three times per week.

Diaphragmatic Training

Other

The therapist will instruct each woman to lie on her back with knees bent, place one hand on her upper chest and the other on her belly. They will breathe in slowly, tighten abdominal muscles, and exhale through pursed lips. Expiration should be relaxed and lightly controlled, and not forceful. Expiration should not be prolonged, and the woman should not initiate inspiration with accessory muscles or upper chest. The session will be repeated 3-4 times, lasting 5-10 minutes, and repeated three times per week for 12 weeks.

Primary outcomes

  1. assessing the change in Urodynamics (first desire to void)

    Time frame: up to 12 weeks

    The study used a double-lumen cytometry catheter to diagnose involuntary detrusor contractions in women. The catheter measured the change in urodynamics in form of volume at first desire to void, for each woman in all groups. The urodynamic method is a reliable and mandatory method for diagnosing and treating UUI symptoms, as relying solely on urinary symptoms may lead to under-diagnosis of detrusor overactivity.

  2. assessing the change in Urodynamics (first sensation of bladder filling)

    Time frame: up to 12 weeks

    The study used a double-lumen cytometry catheter to diagnose involuntary detrusor contractions in women. The catheter measured the change in urodynamics in form of first sensation of bladder filling, for each woman in all groups.

  3. assessing the change in Urodynamics (maximum bladder capacity)

    Time frame: up to 12 weeks

    The study used a double-lumen cytometry catheter to diagnose involuntary detrusor contractions in women. The catheter measured the change in urodynamics in form of maximum bladder capacity, for each woman in all groups.

Secondary outcomes

  1. assessing the change in weight and height

    Time frame: up to 12 weeks

    The study utilized a weight-height scale to measure weight and height for women in all groups (A, B & C) and to calculate BMI before and after treatment.

  2. assessing the change in bladder ascending movement

    Time frame: up to 12 weeks

    Transvaginal ultrasound assessment of bladder and urethra was conducted in the midsagittal plane, determining posterior urethro vesical angle.

  3. assessing the change in Urinary function

    Time frame: up to 12 weeks

    The study uses a self-administered questionnaire to assess urinary function in women in different groups (A, B, and C) at the start and end of the study course. The questionnaire consists of 21 items, each with its own Likert rating scale structure. Each woman is instructed and given appropriate time to answer.

  4. assessing the change in body mass index

    Time frame: up to 12 weeks

    The study utilized a weight-height scale to measure to calculate BMI before and after treatment.

Sponsors and collaborators

Lead sponsor

Cairo University

Other

Registry information

Important dates

Study start
2023
Primary completion
2023
Study completion
2024
First posted
Jul 25, 2024
Registry last updated
Jul 25, 2024

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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