The Relationship Between Osteoporosis and Sarcopenia Parameters in Postmenopausal Women Under 60

NCT ID: NCT07045012

Last Updated: 2025-07-01

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Total Enrollment: 52 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2025-06-25
• Study Completion Date: 2025-07-25

Brief Summary

This cross-sectional study will include postmenopausal women under the age of 60 who visited the Physical Medicine and Rehabilitation outpatient clinic at Beylikdüzü State Hospital between June 25 and July 25, 2025. Participants must have undergone a bone mineral density (BMD) assessment within the past six months using Dual X-ray Absorptiometry (DXA). Both osteoporotic and non-osteoporotic patients will be enrolled. Sociodemographic data such as age, height, weight, and BMI will be recorded. Femoral neck and L1-L4 T-scores and BMD values will be obtained from existing DXA results. Information on osteoporosis treatment, presence of fecal incontinence, constipation, and medication use will be collected. In the second phase, sarcopenia will be assessed according to EWGSOP2 criteria using bioelectrical impedance analysis for skeletal muscle mass, handgrip strength, and the five-time sit-to-stand test. Differences between the osteoporotic and non-osteoporotic groups will be analyzed.

Conditions

Osteoporosis

Study Design

• Observational Model Type: CASE_CONTROL
• Study Time Perspective: CROSS_SECTIONAL

Eligibility Criteria

Inclusion Criteria

• Women under 60 years of age who are postmenopausal.
• Patients with or without a diagnosis of osteoporosis:

Osteoporosis group: T-score ≤ -2.5 in femoral neck or L1-L4 region. Control group: T-score ≥ -1.0 in femoral neck and L1-L4 region.

-Patients who provide written informed consent to participate in the study.

Exclusion Criteria

• Refusal to participate in the study.
• Presence of neuromuscular diseases that could cause muscle loss.
• History of infection, recent surgery, or trauma.
• Presence of psychiatric disorders.
• Cognitive impairment that could interfere with test performance or data reliability.
• Use of medications that could affect study outcomes (e.g., corticosteroids, muscle relaxants, or medications influencing bone/muscle metabolism).

• Minimum Eligible Age: 50 Years
• Maximum Eligible Age: 59 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

Beylikduzu State Hospital

OTHER

Sponsor Role: lead

Responsible Party

Busra Sirin

Principle Investigator

Responsibility Role: PRINCIPAL_INVESTIGATOR

Other Identifiers

Beylikdüzüstateh20

Identifier Type: -

Identifier Source: org_study_id