Heart Bypass Surgery Clinical Trials

Clinical trials related to Heart Bypass Surgery Procedure

The Effect of Patient Education and Implementation of Teleinterventions by Nurses, on the Incidence of Surgical Wound Infections, in Patients After Coronary Artery Bypass Surgery

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The goal of this clinical trial is to determine if nurse-led education and tele-interventions can reduce the incidence of surgical wound infections in patients after coronary artery bypass surgery. The main questions it aims to answer are: * Can nurse-led education reduce the rate of surgical wound infections after coronary artery bypass surgery? * Does the addition of tele-interventions further decrease the incidence of these infections compared to standard care? Researchers will compare three groups: * Group A: Standard postoperative care * Group B: Nurse-led patient education * Group C: Nurse-led patient education plus tele-interventions Participants will: * Receive standard care, nurse-led education, or nurse-led education with tele-interventions * Having regular follow-up as per group assignment * Monitor and report infection during the study period

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Age ≥ 18 years

• Patients who have undergone CABG with median sternotomy

• Proficiency in reading and writing in Greek

• Patients who provide written informed consent for participation in the study

• Patients who have access to a mobile phone and know how to use it

• Patients without difficulties in vision, speech, or hearing

• Patients at intermediate or high risk for developing surgical site infections, based on their scores in the risk stratification models described below

Locations
Other Locations
Greece
Hellenic Mediterranean University
RECRUITING
Heraklion
Contact Information
Primary
Konstantinos Giakoumidakis, RN
kongiakoumidakis@hmu.gr
6973793489
Backup
Paraskevi Kyriazi, RN
ddk224@edu.hmu.gr
6970305170
Time Frame
Start Date: 2024-03-01
Estimated Completion Date: 2025-09-01
Participants
Target number of participants: 220
Treatments
No_intervention: Control group: Group A
No education and implementation of teleinterventions, whereas implementation of standard care based on the existing protocol of the Clinical Department is going to be applied
Experimental: Group B: nurse-led education
The participants in Group B will be guided and trained by the principal investigator based on a specially designed educational booklet. Group B will also receive teleinterventions.
Experimental: Group C: nurse-led education and implementation of teleinterventions
The participants in Group C will be guided and trained by the principal investigator based on a specially designed educational booklet. Group C will also receive teleinterventions and a guidance video will be presented to them
Related Therapeutic Areas
Sponsors
Leads: Hellenic Mediterranean University

This content was sourced from clinicaltrials.gov

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