- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06289738
ICF in Takayasu Arteritis
May 13, 2024 updated by: Elif Gur Kabul, Pamukkale University
Problem Analysis Based on the International Classification of Functioning, Disability and Health in Patients With Takayasu Arteritis
The aim was to analyze the problem in patients with Takayasu Arteritis based on the International Classification of Functioning, Disability and Health.The sample of our study will consist of individuals between the ages of 18-65 who have been diagnosed with Takayasu Arteritis by rheumatologists and are followed by Pamukkale University Rheumatology Clinic.
Study Overview
Study Type
Interventional
Enrollment (Actual)
15
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Uşak, Turkey
- Elif Gur Kabul
-
-
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
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:-Being between the ages of 18-65
- Volunteering to participate in the study
- Being diagnosed with Takayasu Arteritis by a rheumatologist
Exclusion Criteria:- Having another disease that affects your physical condition
- Having cognitive impairment that makes it difficult to cooperate
- Being pregnant
- Having a neurological disease
- Having had any surgery in the last year
- Having another concurrent rheumatic disease
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
- Primary Purpose: Other
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Experimental
Takayasu Arteritis patients between the ages of 18-65
|
Matching the answers given to the question set consisting of 6 open-ended questions with ICF
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
6 open-ended questions
Time Frame: 25 minutes
|
ICF
|
25 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 (Actual)
February 21, 2024
Primary Completion (Actual)
March 20, 2024
Study Completion (Actual)
March 25, 2024
Study Registration Dates
First Submitted
February 24, 2024
First Submitted That Met QC Criteria
February 24, 2024
First Posted (Actual)
March 4, 2024
Study Record Updates
Last Update Posted (Estimated)
May 14, 2024
Last Update Submitted That Met QC Criteria
May 13, 2024
Last Verified
May 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ICF in Takayasu Arteritis
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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