- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05740085
Osteoporosis Awareness in Rheumatoid Arthritis Patients
February 21, 2023 updated by: Mustafa Hüseyin Temel, Uskudar State Hospital
Knowledge and Awareness of Osteoporosis in Rheumatoid Arthritis Patients
Osteoporosis is a condition that describes compromised skeletal microarchitecture in general, with clinical signs of decreased bone mineral density.
Rheumatoid arthritis patients are at increased risk for developing osteoporosis.
It is crucial to identify whether rheumatoid arthritis patients know and know about this disease.
This study investigates awareness and knowledge of osteoporosis in rheumatoid arthritis patients.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed Description
Osteoporosis is a common disease of bone loss.
The reduced bone strength predisposes an increased risk for fractures in older individuals.
It can affect people from different ethnicity.
Many factors increase the risk of osteoporosis, including age, postmenopausal state, glucocorticoid use, low body weight, calcium, vitamin D, immobility, and chronic inflammation.
Patients with rheumatoid arthritis are at high risk of developing osteoporosis due to chronic inflammation and the medications they use.
Patients' knowledge and awareness about osteoporosis are essential for early detection, implementation of lifestyle changes, and treatment compliance.
This study aimed to investigate osteoporosis awareness and knowledge about osteoporosis in patients with rheumatoid arthritis.
Study Type
Observational
Enrollment (Anticipated)
100
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Mustafa H Temel, M.D.
- Phone Number: 05342714872
- Email: mhuseyintemel@gmail.com
Study Locations
-
-
Üsküdar
-
Istanbul, Üsküdar, Turkey
- Üsküdar State Hospital
-
Contact:
- Mustafa H Temel, M.D.
- Phone Number: 05342714872
- Email: mhuseyintemel@gmail.com
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 90 years (Adult, Older Adult)
Accepts Healthy Volunteers
N/A
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Patients aged 18 to 90 years with a diagnosis of rheumatoid arthritis who gave consent to participate in the study.
Description
Inclusion Criteria:
- Clinical diagnosis of rheumatoid arthritis
- Must be between the ages of 18 and 90
- Must give consent to participate in the study
Exclusion Criteria:
• Not giving consent
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Rheumatoid Arthritis Patients
Patients that are diagnosed with rheumatoid arthritis
|
Patients will be asked to fill out a patient information form and an osteoporosis awareness form
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Level of knowledge in osteoporosis
Time Frame: 1 day
|
Level of knowledge in osteoporosis will be assessed with revised osteoporosis knowledge test (OKT).
The Revised OKT (2012) is a comprehensive instrument reflecting current research and assesses osteoporosis knowledge of adults.
Responses offered to participants are multiple choice (e.g., for risk items: more likely, less likely, neutral, don't know), there is only one correct answer for each item.
Responses are dichotomously recoded as correct or incorrect.
In a U.S. sample of adults, the measure demonstrated internal consistency, very good stability, and content validity.
Point-biserial correlations supported the measure's validity.
|
1 day
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: Mustafa H Temel, M.D., Üsküdar State Hospital
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Anticipated)
April 30, 2023
Primary Completion (Anticipated)
July 30, 2023
Study Completion (Anticipated)
August 30, 2023
Study Registration Dates
First Submitted
December 27, 2022
First Submitted That Met QC Criteria
February 21, 2023
First Posted (Estimate)
February 22, 2023
Study Record Updates
Last Update Posted (Estimate)
February 22, 2023
Last Update Submitted That Met QC Criteria
February 21, 2023
Last Verified
February 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- OPRA1
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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