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Study
The purpose of this clinical trial was to investigate the effects of a multi-intervention approach, including Kegel and Tai Chi exercises, on quality of life, self-efficacy, and urinary incontinence severity in postmenopausal women.
Key Questions the Study Aims to Answer:
How does the multi-intervention approach affect quality of life?
Does the multi-intervention approach affect women's self-efficacy?
How does the multi-intervention approach affect urinary incontinence severity?
How does the frequency of exercises (3 days per week vs. 6 days per week) affect these outcomes?
Do the effects of the intervention change temporally over the 8-week period?
Who is Eligible?
Women aged 45 and over who have gone through menopause
Those who wish to volunteer for the study
Those who have no communication barriers
Those who have not previously received treatment for urinary incontinence
Those who can use a smartphone or WhatsApp
Those who experience urine leakage when coughing or sneezing
Study Application:
The exercises will be administered for 8 weeks.
Participants will be taught how to perform the exercises and will be demonstrated through brochures and videos.
Reminders will be provided during the exercises.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Intervention Group 1 (Tai Chi and Kegel, 3 days/week) | Experimental | articipants will perform Tai Chi and Kegel exercises 3 days per week for 8 weeks. |
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| Intervention Group 2 (Tai Chi and Kegel, 6 days/week) | Experimental | Participants will perform Tai Chi and Kegel exercises 6 days per week for 8 weeks. |
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| Control Group | No Intervention | Participants will receive no exercise or educational intervention and will continue their usual daily routines. |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Combined Exercise Program | Behavioral | Participants will receive education on urinary incontinence, Kegel and Tai Chi exercises, brochures and videos, and perform exercises 3 days/week for 8 weeks with reminders |
| Measure | Description | Time Frame |
|---|---|---|
| Urinary Incontinence Severity Measured by [İnkontinans Şiddet İndeksi] | Quality of life related to urinary incontinence will be assessed using a validated questionnaire. Differences from baseline to post-test will be evaluated. | 8 weeks (baseline and post-intervention) |
| Measure | Description | Time Frame |
|---|---|---|
| Quality of Life Related to Urinary Incontinence | Quality of life related to urinary incontinence will be assessed using a validated questionnaire. Differences from baseline to post-test will be evaluated. | 8 weeks (baseline and post-intervention) |
| Self-Efficacy in Managing Urinary Incontinence |
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Inclusion Criteria:
- Being female
Having undergone menopause
Willingness to participate in the study
No communication barriers
Not receiving any treatment for urinary incontinence
Owning a smartphone
Having WhatsApp installed
Experiencing urinary leakage when coughing or sneezing, according to the International Continence Society (ICS) definition
Exclusion Criteria:
Having communication barriers
Not being in menopause
Not owning a smartphone
Not experiencing urinary incontinence
Having received any treatment for urinary incontinence
Having undergone surgical menopause
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| ÅžEYMA SOYANIT ERASLAN | Contact | +90 368 271 57 57 / 6571 | seymasoyanitt@gmail.com |
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| ID | Term |
|---|---|
| D014549 | Urinary Incontinence |
| ID | Term |
|---|---|
| D014555 | Urination Disorders |
| D014570 | Urologic Diseases |
| D052776 | Female Urogenital Diseases |
| D005261 | Female Urogenital Diseases and Pregnancy Complications |
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Participants will be randomly assigned to one of three parallel groups:
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| Combined Exercise Program | Behavioral | Participants will receive same education and materials as Group 1 and perform exercises 6 days/week for 8 weeks with reminders. |
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Participants' self-efficacy will be measured using a validated scale, comparing baseline and post-test scores. |
| Baseline and 8 weeks post-intervention |
| D000091642 | Urogenital Diseases |
| D052801 | Male Urogenital Diseases |
| D059411 | Lower Urinary Tract Symptoms |
| D020924 | Urological Manifestations |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |