Actively Recruiting
Kinesiophobia in Patients With Implanted Left Ventricular Assist Devices
Led by Marmara University · Updated on 2026-02-10
37
Participants Needed
1
Research Sites
61 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this prospective and cross-sectional observational study is to learn if the presence and changes in kinesiofobia (fear of movement) affect functional capacity levels in heart failure patients who are transplant candidates and have been implanted with a Left Ventricular Assist Device (LVAD). The main questions it aims to answer are: i) Does the level of kinesiofobia change significantly 1 month after LVAD implantation? ii) Do changes in kinesiofobia levels predict changes in functional exercise capacity (measured by the 2-Minute Walk Test and 30-Second Sit-to-Stand Test)? Researchers will compare pre-discharge (baseline) measurements to 1-month post-discharge follow-up measurements to see if improvements in kinesiofobia correlate with improved functional mobility and endurance. Participants will: i) Complete the Tampa Scale of Kinesiofobia (TSK) to assess their fear of movement. ii) Perform the 2-Minute Walk Test (2MWT) to evaluate functional exercise capacity and mobility. iii) Perform the 30-Second Sit-to-Stand Test (30STS) to determine functional endurance and lower extremity performance. iv) Receive standardized physical activity recommendations upon discharge. v) Return for a follow-up assessment one month later to repeat the same battery of tests.
CONDITIONS
Official Title
Kinesiophobia in Patients With Implanted Left Ventricular Assist Devices
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Being a heart transplant candidate and having undergone LVAD implantation
- Having a left ventricular ejection fraction (LVEF) <30%
- Not having developed any surgical or medical complications in the early period after implantation
- Being referred to the study by a cardiologist at the time of discharge
- Being able to read and write and volunteering to participate in the study.
You will not qualify if you...
- Those with evidence of active infection following implantation
- Psychiatric problems developing after LVAD implantation that interfere with cognitive adaptation
- Musculoskeletal problems developing after LVAD implantation
- Cases experiencing acute cardiac problems requiring hospitalization during follow-up
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Marmara University Faculty of Health Sciences
Istanbul, Turkey (Türkiye), 34854
Actively Recruiting
Research Team
R
Rafet Umut Erdoğan
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
SCREENING
Number of Arms
1
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