Stress Urinary Incontinence and Sarcopenia in Postmenopausal Osteoporosis
Recruiting · NCT06655701 · Observational (researchers observe without assigning treatment) · Lead sponsor: Beylikduzu State Hospital
View the official record on ClinicalTrials.gov →Interventions studied
No intervention
What this trial is about
The primary aim of our study is to evaluate the presence of stress urinary incontinence in postmenopausal patients with and without osteoporosis, determine its impact on quality of life, and explore its relationship with sarcopenia.
Who can take part
Age range
50 Years to 75 Years
Sex
Female
Healthy volunteers
Yes - healthy volunteers may be accepted
Phase
Not specified
Study type
Observational (researchers observe without assigning treatment)
Inclusion criteria
- Postmenopausal women with DXA measurements performed within the last 6 months.
- Based on DXA measurements:
- Femoral neck and L1-L4 T-scores of -1 and above will be included in the control group (non-osteoporotic).
- Femoral neck and L1-L4 T-scores of -2.5 and below will be included in the osteoporosis group.
- Aged 50-75 years
Exclusion criteria
- Refusal to participate in the study.
- History of neurological diseases, infections, surgeries, or trauma that could cause urinary incontinence or muscle loss.
- Presence of psychiatric disorders.
- Cognitive impairments.
- Use of medications that could affect the study results.
Where it is running
1 location listed.
- Beylikdüzü State Hospital - Istanbul, Turkey (Türkiye)