Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07528482

Effects of Reflexology and Cold Application Before Chest Tube Removal in CABG Patients

Led by Ankara University · Updated on 2026-04-14

108

Participants Needed

1

Research Sites

20 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims to evaluate the effects of combined reflexology and cold application on pain, anxiety, and physiological parameters in patients undergoing chest tube removal (CTR) after coronary artery bypass grafting (CABG) surgery. Chest tube removal is an invasive procedure that often causes significant pain and anxiety, which can negatively impact the recovery process. In this randomized controlled trial, patients will be assigned to a combined intervention group (reflexology and cold application) or a control group. The study seeks to provide evidence-based recommendations for non-pharmacological nursing interventions to improve patient comfort and reduce complications during the post-operative period.

CONDITIONS

Official Title

Effects of Reflexology and Cold Application Before Chest Tube Removal in CABG Patients

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Being 18 years of age or older
  • Not having undergone previous open heart surgery
  • Not having received analgesics within 4 hours prior to the procedure
  • Having a VAS pain score of 3 or higher
  • Voluntary participation in the study
Not Eligible

You will not qualify if you...

  • Being under 18 years of age
  • Using inotropic drugs
  • Having a history of chronic pain
  • Having a history of alcohol or drug use
  • Having a psychiatric illness
  • Having skin lesions, burns, or wounds on the feet that would prevent massage application

AI-Screening

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Trial Site Locations

Total: 1 location

1

Gulhane Training and Research Hospital

Ankara, Turkey (Türkiye), 06010

Actively Recruiting

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Research Team

N

neriman yükseltürk şimşek, assistant prof.

CONTACT

Y

yasemin özkan, phd

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

3

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