Actively Recruiting
The Investigation of the Effectiveness of Virtual Reality Applications in Postmenopausal Osteoporosis Patients
Led by Kirsehir Ahi Evran Universitesi · Updated on 2026-02-27
50
Participants Needed
1
Research Sites
14 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Osteoporosis is a progressive disease characterised by a decrease in bone mass, deterioration in bone microarchitecture, and increased fragility. Etiologically, it is divided into two types: primary (postmenopausal and senile) and secondary. Postmenopausal women are particularly at high risk; it is seen in more than 80% of women over the age of 50 and in almost all individuals over the age of 75. With menopause, bone mineral density decreases, which negatively affects neuromuscular functions, leading to balance disorders, decreased walking speed, and an increased risk of falls. Falls are the primary cause of osteoporotic fractures and result in functional loss, morbidity, mortality, and increased healthcare costs. Exercise is effective in reducing bone loss; in recent years, therapeutic virtual reality and exercise games (exergames) have come to the fore. However, the literature on the effectiveness of these applications in postmenopausal osteoporosis patients is limited. The aim of this study is to investigate the effects of virtual reality applications on balance, quality of life, and fall risk and to compare them with a control group.
CONDITIONS
Official Title
The Investigation of the Effectiveness of Virtual Reality Applications in Postmenopausal Osteoporosis Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Postmenopausal women aged 50-75 years
- Diagnosed with osteoporosis by DEXA measurement (T-score 2.5 or lower)
- Menopause for at least 1 year
- Able to walk independently without assistive devices
- Volunteered and provided informed consent
- Adequate cognitive function (Mini Mental Test score 24 or higher)
You will not qualify if you...
- Secondary osteoporosis from endocrine, metabolic, or drug causes
- Lower limb fracture or surgery within last 6 months
- Severe cardiovascular, neurological, or musculoskeletal disorders
- Vestibular or visual impairments affecting balance
- Intolerance to virtual reality (e.g., dizziness, nausea)
- Participation in regular physiotherapy or exercise program within last 3 months
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Kırşehir Ahi Evran University
Center, Kirşehi̇r, Turkey (Türkiye), 40100
Actively Recruiting
Research Team
İ
İrem CANLI, Ph.D.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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