Actively Recruiting

Phase Not Applicable
Age: 18Years - 75Years
All Genders
NCT06551714

The Effect of Neurophysiological Facilitation Techniques on Health Parameters in Early Stages After Open Heart Surgery

Led by Dogus Universitesi · Updated on 2024-08-13

32

Participants Needed

1

Research Sites

43 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

In this study, researchers aimed to investigate effects of neurophysiological facilitation on functional capacity and respiratory parameters of patients who underwent open heart surgery. Do neurophysiological facilitation techniques improve individuals' respiratory parameters more than phase 1 cardiac rehabilitation? Do neurophysiological facilitation techniques improve individuals' functional capacity more than phase 1 cardiac rehabilitation? Researchers will apply phase 1 cardiac rehabilitation to both groups to see the effectiveness of neurophysiological facilitation techniques.

CONDITIONS

Official Title

The Effect of Neurophysiological Facilitation Techniques on Health Parameters in Early Stages After Open Heart Surgery

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Having open heart surgery for the first time
  • Being between the ages of 18-75
  • Being fully cooperative
Not Eligible

You will not qualify if you...

  • Having facial, sternum and rib fractures
  • Having chronic renal failure
  • Development of cerebrovascular accident
  • Having cognitive dysfunction
  • Development of deep vein thrombosis in the post-operative period
  • Having neuromuscular disease
  • Having an orthopedic disability
  • Intubation time longer than 24 hours
  • Staying in intensive care for more than 48 hours

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

Lokman Hekim Akay Hospital

Ankara, Turkey (Türkiye), 06000

Actively Recruiting

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Research Team

F

Feyza merakli

CONTACT

G

Gungor

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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