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RECRUITINGINTERVENTIONAL

Kinesiophobia in Patients With Implanted Left Ventricular Assist Devices

Kinesiophobia Affects Functional Capacity in Patients With Implanted Left Ventricular Assist Devices

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

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.

Who May Be Eligible (Plain English)

Who May Qualify: - 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. Who Should NOT Join This Trial: - 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. Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * 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. Exclusion Criteria: * 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.

Treatments Being Tested

DIAGNOSTIC_TEST

Physical Activity Recommandations

Patients with implanted LVADs will be given recommendations for physical activities they can incorporate into their daily lives.

Locations (1)

Marmara University Faculty of Health Sciences
Istanbul, Turkey (Türkiye)