Evaluation of the efficacy of using the pelvic floor muscle training application in comparison with physiotherapy

Evaluation of the efficacy of using the pelvic floor muscle training application in comparison with physiotherapy in patients with urinary incontinence

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20210928052626N1

Enrollment

Registered

2022-11-27

Start date

2022-10-23

Completion date

Unknown

Last updated

2023-02-07

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

Conditions

stress or mixed urinary incontinence. Stress incontinence (female) (male)

Interventions

Intervention 1: intervention group: our designed application is used to train the intervention group with kegel exercises for three months and 30 minutes each day. Intervention 2: Control group: these

Eligibility

Sex/Gender

Female

Age

18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Age : 18-70 y/o Female Urinary incontinence for at least once a week Diagnosed stress or mixed incontinence Vaginal prolapse grade 1 or 2 BMI=20-30

Exclusion criteria

Exclusion criteria: Difficulty urinating Pregnancy Macroscopic hematuria Urinary symptoms related to grade 3 or 4 of POP

Design outcomes

Primary

Measure	Time frame
The score obtained in the International Consultation on Incontinence Questionnaire Lower Urinary Tract Symptoms Quality of Life. Timepoint: The beginning of the study (before the start of the intervention) and three months after its start. Method of measurement: The ICIQ-LUTS-qol questionnaire.;The score obtained in the International Consultation on Incontinence Questionnaire - Short Form. Timepoint: The beginning of the study (before the start of the intervention) and three months after its start. Method of measurement: International Consultation on Incontinence Questionnaire - Short Form questionnaire.	—

Measure

Time frame

The score obtained in the International Consultation on Incontinence Questionnaire Lower Urinary Tract Symptoms Quality of Life. Timepoint: The beginning of the study (before the start of the intervention) and three months after its start. Method of measurement: The ICIQ-LUTS-qol questionnaire.;The score obtained in the International Consultation on Incontinence Questionnaire - Short Form. Timepoint: The beginning of the study (before the start of the intervention) and three months after its start. Method of measurement: International Consultation on Incontinence Questionnaire - Short Form questionnaire.

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaede Safari

Esfahan University of Medical Sciences

safari.maede@yahoo.com+98 31 3668 0048

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026