Stress Urinary Incontinence and Sarcopenia in Postmenopausal Osteoporosis

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age50-75
SponsorBeylikduzu State Hospital

About this trial

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.

Eligibility criteria

Qualifiers

Postmenopausal women with DXA measurements performed within the last 6 months.

Aged 50-75 years

Disqualifiers

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.

Trial design

Treatments tested in this trial

  • No intervention

Treatment groups

100 Participants
are divided into 2 treatment groups

Sponsors and collaborators