Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
ID06652061

Development and Evaluation of an Artificial Intelligence Model for Bone Mineral Density Prediction From X-Ray Images

Led by Bangladesh University of Engineering and Technology · Updated on 2024-10-22

600

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

B

Bangladesh University of Engineering and Technology

Lead Sponsor

I

Ibn Sina Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

Osteoporosis is a widespread bone condition that weakens bones and increases fracture risk, posing a major health and economic challenge globally. This research focuses on developing an artificial intelligence (AI) model to predict bone mineral density (BMD) from X-ray images, aiming to improve early osteoporosis detection especially in places like Bangladesh where the standard DEXA scan is scarce and costly. The goal is to create a reliable screening tool that can assist in preventing fractures by enabling earlier diagnosis and treatment. The study collects both retrospective and prospective data from patients undergoing hip and spine X-rays and DEXA scans at a radiology center in Bangladesh. Using convolutional neural networks, the AI model will analyze these X-ray images along with clinical data such as age, gender, menopausal status, and comorbidities to predict BMD. The model's accuracy will be evaluated by comparing predictions to actual DEXA results using several statistical measures and cross-validation methods to ensure consistency. Participants will include adults of all genders with varying bone density levels, including normal, low bone mass, and osteoporosis. Data collected will include demographic, clinical history, imaging, and diagnostic results. The study will monitor primary outcomes like BMD measurements of hip and spine, along with secondary outcomes such as WHO osteoporosis classification and fracture risk assessments over about six months. The final AI tool is intended to support clinicians in identifying osteoporosis earlier and prioritizing patients for further testing, potentially improving care in resource-limited settings.

CONDITIONS

Brief Title

AI Model for Bone Mineral Density Prediction From X-Ray Images

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Female and male patients aged 18 and above
  • Willingness to participate with informed consent for use of X-ray images and clinical data
  • Availability of both hip and spine X-ray images along with DEXA scan results
  • Access to additional medical records related to fractures, pregnancies, and osteoporosis factors
Not Eligible

You will not qualify if you...

  • Incomplete or poor-quality X-ray images or clinical data
  • Medical conditions significantly affecting bone density aside from osteoporosis, such as bone cancers or metabolic diseases
  • Prior treatments or surgeries impacting bone density measurement, including long-term steroid use or recent orthopedic surgeries
  • Pregnancy
  • Presence of hip or spine implants

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person) for consent and eligibility assessment

Diagnostic Evaluation

Duration - Day 1

Participants undergo hip and spine X-ray imaging and DEXA scans to collect bone mineral density data and clinical information.

1 visit (in-person) for X-ray and DEXA scans

Long-term Monitoring

Duration - Approximately 6 months

Participants' bone health is observed through assessment of fracture risk and WHO classification over the study period.

Follow-up assessments as part of routine care over 6 months

Trial Site Locations

Total: 1 location

1

Ibn Sina Diagnostic Centre, Uttara

Dhaka, Bangladesh, 1230

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Research Team

T

Taufiq Hasan, PhD

F

Farihin Rahman, B.Sc

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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