Comfort Theory-Based Nursing Interventions in Women With Stress Urinary Incontinence
Urinary Incontinence
About this trial
This is an interventional supportive care trial for Urinary Incontinence focused on measuring Urinary Incontinence, Comfort Theory, Yoga, Nursing
Eligibility Criteria
Inclusion Criteria:
- 18 years and over
- Diagnosed with SUI
- Continuing to experience UI complaints for at least 3 months
- Who agreed to participate in the research
Exclusion Criteria:
- Diagnosed with pelvic organ prolapse
- Experienced urinary tract infection or hematuria more than 3 times in the last 1 year
- Having major neurological health problems
- Pelvic cancer patient
- Having chronic pelvic pain
- BMI>35 kg/m2
- Having a history of urinary system surgery
- Having yoga experience in the last 1 year
- Actively doing pelvic floor exercises
- Have given birth in the last 6 months
- Pregnancy
- Having limited movement
- Alcohol/drug addiction
Sites / Locations
- Akdeniz UniversityRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Intervention Group
Control Group
After the first interview with the patients in the intervention group, a phone call will be made for regarding the implementation of nursing interventions based on the Comfort Theory, and they will be informed about the planned dates for the implementation. The implementation phase of nursing interventions based on Comfort Theory will be carried out for 6 weeks at the Communication Laboratory of the Faculty of Nursing of Akdeniz University on the planned dates with the patients. In addition, a handbook will be given to the patients at the beginning of the practice, and the Home Yoga Diary in the handbook will be expected to be filled in daily by the patients during the research. Immediately after the implementation of the nursing interventions based on Comfort Theory (week 6), patients will be asked to fill in ISI, IQO-L, and the Urinary Incontinence and Frequency Comfort Scale. During this whole process, patients will continue their planned routine care and treatment.
After the first interview with the patients in the control group, the routine care and treatment practices planned by the polyclinic physician and nurse will continue. No additional intervention is planned for the patients in this group. A new interview will be planned with the patients in the control group 6 weeks after the first interview, and they will be asked to fill in the ISI, IQO-L, and the Urinary Incontinence and Frequency Comfort Scale.