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Clinical Trials in Turkey / NCT07264712
Active, not recruiting Not applicable

The Effect of Wound Care Education Given to Patients on Wound Care Knowledge, Self-Care Self-Efficacy, and Quality of Recovery

NCT07264712 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-10-10
Last updated
2026-05-26

Condition(s) studied

Prosthetic TreatmentWound CareEducation

Investigational drug(s) / intervention(s)

artificial intelligence-supported education

artificial intelligence-supported education: The purpose of the study will be explained to the individuals in the experimental group using a face-to-face interview technique, and a patient introduction form will be administered by the researcher one day before surgery. The researcher will then provide patients with visual and verbal wound care training using the "Surgical Patient Wound Care Guide," and the educational materials will be provided. To assess the effectiveness of the training, a Knowledge Level Survey consisting of 10 true/false questions will be administered to patients on the third postoperative day. Two weeks after surgery, the Patient Follow-up Form, Self-Care Self-Efficacy Scale, and Quality of Healing Scale will be completed by phone.

Study summary

This study will be conducted as a randomized controlled trial to determine the impact of artificial intelligence-assisted wound care training provided to patients undergoing prosthetic surgery on their wound care knowledge, quality of healing, and self-care self-efficacy. It was planned to include 22 individuals in the experimental group and 22 in the control group. However, considering the potential for data loss, the study was planned to be completed with a total of 50 individuals: 25 in the experimental group and 25 in the control group. Patient Identification Form, Patient Follow-up Form, Knowledge Level Questionnaire, Self-Care Self-Efficacy Scale and Quality of Recovery (QoR-15) Scale were used to collect data.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Those undergoing total hip or knee replacement surgery * Those who volunteer to participate in the study * Those over 18 years of age * Those who have no communication problems (language, hearing impairment, etc.) Exclusion Criteria: * Patients who have developed a surgical site infection * Illiterate * Unable to self-care * Previously had prosthetic surgery will not be included.

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Erciyes University Kayseri Melikgazi
Health training and research hospital Kayseri Melikgazi

More TC Erciyes University trials in Turkey

Other trials for the same condition

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 NCT07264712 on ClinicalTrials.gov ↗ ← All trials in Turkey