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Tests treatment safety and results for Osteoperosis
Official title The Investigation of the Effectiveness of Virtual Reality Applications in Postmenopausal Osteoporosis Patients
ClinicalTrials.gov ID: NCT07231822
What this study is testing
- What it's testing
- 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.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 40 to 65. Healthy volunteers may be eligible.
You may be able to join if
- Postmenopausal women aged 50-75 years
- Individuals diagnosed with osteoporosis based on Dual-Energy X-ray Absorptiometry (DEXA) measurement (T-score ≤ -2.5)
- Having been in menopause for at least 1 year
- Being able to walk independently (without the use of assistive devices)
- Volunteering to participate in the study and having provided informed consent
You likely can't join if
- Secondary osteoporosis diagnosis (e.g. endocrine, metabolic or drug-induced causes)
- History of lower limb fracture or surgical intervention within the last 6 months
- Individuals with severe cardiovascular, neurological, or musculoskeletal disorders
- Individuals with vestibular or visual impairments that may affect balance
- Intolerance to virtual reality applications (e.g., dizziness, nausea, etc.)
- Individuals who have participated in a regular physiotherapy or exercise programme within the last 3 months
See the full eligibility criteria
- Postmenopausal women aged 50-75 years
- Individuals diagnosed with osteoporosis based on Dual-Energy X-ray Absorptiometry (DEXA) measurement (T-score ≤ -2.5)
- Having been in menopause for at least 1 year
- Being able to walk independently (without the use of assistive devices)
- Volunteering to participate in the study and having provided informed consent
- Having adequate cognitive function (e.g., Mini Mental Test ≥ 24)
- Secondary osteoporosis diagnosis (e.g. endocrine, metabolic or drug-induced causes)
- History of lower limb fracture or surgical intervention within the last 6 months
- Individuals with severe cardiovascular, neurological, or musculoskeletal disorders
- Individuals with vestibular or visual impairments that may affect balance
- Intolerance to virtual reality applications (e.g., dizziness, nausea, etc.)
- Individuals who have participated in a regular physiotherapy or exercise programme within the last 3 months
The study team makes the final eligibility decision.
Where it's taking place
- Center, Kirşehi̇r, Turkey (Türkiye)
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 40 years to 65 years. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Center, Kirşehi̇r, Turkey (Türkiye). Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.