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Clinical Trials in Turkey / NCT07528482
Recruiting Not applicable

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

NCT07528482 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-12-15
Last updated
2026-04-14

Condition(s) studied

Pain, Acute Post-OperativeAnxietyChest Tube RemovalCoronary Artery Bypass

Investigational drug(s) / intervention(s)

ReflexologyCryotherapy alone

Reflexology: A trained researcher will apply foot reflexology for 40 minutes (20 minutes per foot) prior to chest tube removal. The intervention focuses on specific reflex points on the soles, dorsum, and toes of both feet to reduce pain and anxiety

Cryotherapy alone: A 13 cm x 13 cm cold pack, frozen for at least 2 hours at -20°C/-30°C, will be applied to the skin at the chest tube insertion site for 20 minutes before removal. The area will be covered with a gauze pad to prevent direct contact with the skin

Study summary

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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * 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 Exclusion Criteria: * 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

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Gulhane Training and Research Hospital Ankara Turkey (Türkiye) Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07528482 on ClinicalTrials.gov ↗ ← All trials in Turkey