Actively Recruiting

Phase Not Applicable
All Genders
NCT07394621

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

All Genders

Eligibility Criteria

Eligible

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.
Not Eligible

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

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Marmara University Faculty of Health Sciences

Istanbul, Turkey (Türkiye), 34854

Actively Recruiting

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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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