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Clinical Trials in Turkey / NCT07348497
Active, not recruiting Not applicable

Effects of Preoperative Education on Anxiety and Emergence Agitation

NCT07348497 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-12-12
Last updated
2026-01-16

Condition(s) studied

Preoperative AnxietyEmergence AgitationSurgical Patients

Investigational drug(s) / intervention(s)

Preoperative Emergence-Focused EducationStandard Perioperative Care

Preoperative Emergence-Focused Education: A standardized preoperative educational intervention delivered by trained nurses to increase patients' understanding of the anesthesia emergence process and to reduce preoperative anxiety and postoperative emergence agitation. The intervention is provided before surgery through verbal education and written materials.

Standard Perioperative Care: Routine perioperative care provided according to institutional standards, including standard preoperative verbal information.

Study summary

This randomized controlled trial aims to evaluate the effect of structured preoperative education focused on the anesthesia emergence process on preoperative anxiety and postoperative emergence agitation in adult surgical patients undergoing general anesthesia. Emergence agitation is a frequent postoperative complication associated with patient discomfort, safety risks, and increased clinical workload. Preoperative anxiety is considered a modifiable risk factor for emergence agitation; however, evidence-based educational interventions targeting the emergence phase are limited.

The intervention consists of a standardized, nurse-led preoperative education program providing information on general anesthesia, endotracheal intubation and extubation, the post-anesthesia care unit environment, and expected physical and emotional responses during emergence. Education is delivered through a face-to-face individual session supported by written materials. Patients in the control group receive routine perioperative verbal information in accordance with standard care.

Eligible adult patients scheduled for elective general surgery under general anesthesia will be randomly assigned to either the intervention or control group. Preoperative anxiety will be assessed using the Amsterdam Preoperative Anxiety and Information Scale (APAIS). Emergence agitation will be evaluated in the post-anesthesia care unit using the Riker Sedation-Agitation Scale (SAS) and the Richmond Agitation-Sedation Scale (RASS) during the first 30 minutes after surgery.

The primary outcomes are preoperative anxiety levels and the incidence of postoperative emergence agitation. Secondary outcomes include postoperative pain, extubation time and quality, and length of stay in the post-anesthesia care unit. This study seeks to determine whether emergence-focused preoperative education can improve perioperative psychological outcomes and enhance patient safety in surgical care.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * Age 18 years or older * Scheduled for elective general surgery under general anesthesia * American Society of Anesthesiologists (ASA) physical status I-III * Able to comprehend the educational intervention * Willing and able to provide written informed consent Exclusion Criteria: * History of neurological disorders, cognitive impairment, or dementia * Severe psychiatric illness or current use of antipsychotic medications * Alcohol or substance use disorder * Sensory impairments (visual, hearing, or speech) that may interfere with communication

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Sultan 2.Abdul Hamid Khan Educational and Research Hospital Istanbul Üsküdar

More Yeditepe 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 NCT07348497 on ClinicalTrials.gov ↗ ← All trials in Turkey