Urinary incontinence. Unspecified urinary incontinence
Conditions
Interventions
Intervention 1: Intervention group: The RF+ PFMT group receives five radiofrequency therapy sessions as weekly sessions, with the settings that will be mentioned below, and 15 sessions of pelvic floor
Sponsors
University of social welfare and rehabilitation sciences
Eligibility
Sex/Gender
Female
Age
35 Years to 55 Years
Inclusion criteria
Inclusion criteria: - Women aged 35 to 55 with urinary incontinence as the main clinical complaint, whose urine loss of more than 1 gram per hour can be confirmed by the test pad, and who have sexual disorders and impotence at the same time.
Exclusion criteria
Exclusion criteria: Patients with chronic degenerative diseases that affect muscle and nerve tissues. Presence of any degree of pelvic organ prolapse Active or frequent urinary tract infections Vulvovaginitis Atrophic vaginitis Absence of a copper IUD in the uterus Patients who are pregnant or have given birth less than 6 months ago. Type 1 and 2 diabetes neurological disease Mental illness taking drugs that affect urination History of surgical or drug treatment for urinary incontinence Chronic debilitating diseases such as kidney failure Those who have a pacemaker. If the patient does not want to continue to cooperate at any stage of the study, does not complete the treatment sessions, and the patient's condition changes in such a way that they lose any of the entry criteria, the participants will be excluded from the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Performance (strength and tolerance) of the pelvic floor muscles. Timepoint: Before the start of the intervention, the end of the last session of the intervention, one month later. Method of measurement: using perineometer device.;The quantitive amount of urine lost. Timepoint: Before the start of the intervention, the end of the last session of the intervention, one month later. Method of measurement: using one hour pad test.;Incontinence symptoms and sexual function. Timepoint: Before the start of the intervention, the end of the last session of the intervention, one month later. Method of measurement: Using the valid Persian version of ICIQ-SF, ICIQ-VS, FSFI questionnaires.;Satisfaction with treatment. Timepoint: Before the start of the intervention, the end of the last session of the intervention, one month later. Method of measurement: using Likert scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactNahid Rahmani
University of social welfare and rehabilitation sciences
Outcome results
None listed