Operating Room Orientation Video Education in Patients Undergoing Prostate Surgery

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexMale
Age18+
SponsorOndokuz Mayıs University

About this trial

This study aims to evaluate the effect of operating room orientation video education delivered at different time points on postoperative pain and state anxiety in patients undergoing surgery for benign prostatic hyperplasia. Patients undergoing transurethral resection of the prostate or holmium laser enucleation of the prostate will be randomly assigned to one of three groups: video education one day before surgery in the surgical ward, video education approximately 30 minutes before surgery in the operating room waiting unit, or routine preoperative information. Pain and state anxiety will be assessed at predefined preoperative and postoperative time points.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Being conscious and able to communicate. Being able to read and understand Turkish. Voluntarily agreeing to participate in the study and providing informed consent.

Disqualifiers

Having a diagnosed psychiatric disorder. Having a chronic pain syndrome. Being scheduled for emergency surgery. Having previously received similar operating room orientation education.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Operating Room Orientation Video Education

    Behavioral

    A 5-minute video-based educational intervention designed to familiarize patients with the operating room environment and the perioperative process. The video includes information about the operating room environment, operating table, patient positioning, information related to the surgical process, the post-anesthesia care unit, and patient transfer.

  • Routine Preoperative Information

    Behavioral

    Participants will receive routine preoperative information according to standard clinical practice without the study-specific operating room orientation video.

Treatment groups

126 Participants
are divided into 3 treatment groups
Group A: Ward Video Education GroupExperimental treatment 1 intervention
Group B: Operating Room Waiting Unit Video Education GroupExperimental treatment 1 intervention
Group C: Routine Information Control GroupActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Postoperative state anxiety

State anxiety will be assessed using the State-Trait Anxiety Inventory-State Anxiety Scale (STAI-S), based on the Turkish adaptation by Necla Öner and Ayhan Le Compte. The scale consists of 20 items and yields a total score ranging from 20 to 80, with higher scores indicating greater state anxiety and therefore a worse outcome. State anxiety will be assessed one day before surgery in the surgical ward, before video education in the operating room waiting unit, and 6 hours after surgery in the surgical ward. The primary postoperative outcome will be the State-Trait Anxiety Inventory-State Anxiety Scale score measured 6 hours after surgery.

Time frame
From baseline to 6 hours after surgery
2

Postoperative pain intensity

Pain intensity will be assessed using the Visual Analog Scale (VAS). The scale ranges from 0 to 10, where 0 indicates no pain and 10 indicates the worst imaginable pain. Higher scores indicate greater pain intensity and therefore a worse outcome. Pain intensity will be assessed one day before surgery in the surgical ward, before video education in the operating room waiting unit, and 6 hours after surgery in the surgical ward. The primary postoperative outcome will be the Visual Analog Scale score measured 6 hours after surgery.

Time frame
From baseline to 6 hours after surgery

Secondary outcomes

Other outcomes

Sponsors and contacts

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