Prevelance of Frailty and Its Associated Factors in Patients With Axial Spondyloarthritis
NCT ID: NCT05010720
Last Updated: 2022-07-05
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
100 participants
OBSERVATIONAL
2021-08-12
2022-02-10
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Frailty is a syndrome characterized by decline in physiological reserve and loss of muscle strength. Frailty can lead to vulnerability of individuals to possible injuries and a decrease in independence, and ultimately an increase in mortality. Although frailty is associated with older adults, it has been reported that it can be detected in patients with cancer, diabetes and rheumatological diseases and it is not related with age. Frailty has been reported to be a reversible and a treatable condition.
The aim of our study was to investigate the prevalence of frailty and the relationship between frailty and disease activity, physical functional level, quality of life and other associated factors in individuals with Axial Spondyloarthritis.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Investigation of Central Sensitization Frequency and Related Factors in Axial Spondyloarthritis Patients
NCT04485078
Work Productivity and Social Activities In Patients With Ankylosing Spondylitis
NCT04749537
Comparison of Tele-rehabilitation or Video-Based Core Exercises in Individuals With Axial Spondyloarthritis
NCT06000072
Fatigue and Skeletal Muscle Impact in Severe Axial Spondyloarthritis
NCT03940911
Alexithymia in Ankylosing Spondylitis
NCT04320459
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_ONLY
CROSS_SECTIONAL
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* To be between the ages of 40-65
Exclusion Criteria
* Being diagnosed with newly defined or recurrent cancer,
* Not having enough cognitive skills to answer the questions,
* Having neurological problems such as stroke
* Having cognitive impariment
40 Years
65 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Acibadem University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Özgül Öztürk
Assistant Professor
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Haydarpaşa Numune Research and Training Hospital
Istanbul, , Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
ATADEK 2021/14
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.