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Clinical Trials/NCT06640699
NCT06640699
Not yet recruiting
Not Applicable

The Effects of Neurophysiological Facilitation Techniques on Cardiopulmonary Parameters After Coronary Artery Bypass Graft Surgery

Istanbul University - Cerrahpasa (IUC)0 sites36 target enrollmentNovember 1, 2024
ConditionsCardiac Disease

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cardiac Disease
Sponsor
Istanbul University - Cerrahpasa (IUC)
Enrollment
36
Primary Endpoint
ecocardiography device
Status
Not yet recruiting
Last Updated
last year

Overview

Brief Summary

The aim of the study is to investigate the effects of neurophysiological facilitation techniques, applied in addition to Phase I cardiac rehabilitation in the early postoperative period after coronary artery bypass graft (CABG) surgery, on left ventricular function, respiratory functions, and functional capacity.

Detailed Description

In this prospective randomized controlled study, participants will be randomly divided into two groups: the control group, which will receive Phase I cardiac rehabilitation, and the treatment group, which will receive Phase I cardiac rehabilitation along with the application of neurophysiological facilitation techniques. The participants' left ventricular function, respiratory functions, and functional capacity will be assessed before and after the interventions.

Registry
clinicaltrials.gov
Start Date
November 1, 2024
End Date
March 1, 2025
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Istanbul University - Cerrahpasa (IUC)
Responsible Party
Principal Investigator
Principal Investigator

Gamze Aydin

Principal Investigator

Istanbul University - Cerrahpasa (IUC)

Eligibility Criteria

Inclusion Criteria

  • First-time undergoing open-heart surgery
  • Aged between 50 and 85 years
  • Full cooperation

Exclusion Criteria

  • Presence of facial, sternum, or rib fractures
  • Chronic renal failure
  • Development of cerebrovascular events
  • Cognitive function impairment
  • Development of deep vein thrombosis in the postoperative period
  • Presence of neuromuscular disease
  • Presence of orthopedic disabilities
  • Intubation duration longer than 24 hours
  • Staying in intensive care for more than 48 hours

Outcomes

Primary Outcomes

ecocardiography device

Time Frame: 3 months

ejection fraction will assess with ecocardiography.

spirometer

Time Frame: 3 months

respiratory function test will assess with spirometer

6 Minutes walking test

Time Frame: 3 months

functional capacity will assess with 6 minutes walk test.

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