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NCT Number: NCT07778355

Operating Room Orientation Video Education in Patients Undergoing Prostate Surgery

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.

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Key information

Age range

18 year and older

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

Ondokuz Mayıs University Health Practice and Research Center

Samsun, Atakum, 55500, Turkey (Türkiye)

Location contact

Beyza Çakır

CONTACT

[email protected]

+905372600955

Beyza Çakır

PRINCIPAL_INVESTIGATOR

Özge İşeri, Associate professor

SUB_INVESTIGATOR

About this study

The study will evaluate whether the timing of operating room orientation video education influences postoperative pain and state anxiety in patients undergoing surgery for benign prostatic hyperplasia. The intervention consists of a 5-minute video designed to familiarize patients with the perioperative environment and expected procedures. The video includes information about the operating room environment, the operating table, patient positioning, information related to the surgical process, the post-anesthesia care unit, and patient transfer.

Participants will be randomly allocated in a 1:1:1 ratio to one of three parallel groups. Participants in the first intervention group will receive the video approximately one day before surgery in the surgical ward. Participants in the second intervention group will receive the same video approximately 30 minutes before surgery in the operating room waiting unit. Participants in the control group will receive routine preoperative information according to standard clinical practice.

Pain intensity will be assessed using the Visual Analog Scale, and state anxiety will be assessed using the State-Trait Anxiety Inventory-State Anxiety Scale. Assessments will be performed one day before surgery, before the intervention in the operating room waiting unit, and six hours after surgery in the surgical ward.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Having no visual or hearing impairment that would interfere with viewing the educational video or completing the study assessments.

Undergoing prostate surgery for the first time. Being 18 years of age or older.

Exclusion criteria

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

Treatment and study plan

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.

Primary outcomes

  1. Postoperative state anxiety

    Time frame: From baseline to 6 hours after surgery

    State anxiety will be assessed using the State-Trait Anxiety Inventory-State Anxiety Scale (STAI-S), using the Turkish adaptation by Necla Öner and Ayhan Le Compte. 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 assessment will be the STAI-S score at 6 hours after surgery.

  2. Postoperative pain intensity

    Time frame: From baseline to 6 hours after surgery

    Pain intensity will be assessed using the Visual Analog Scale (VAS). Pain 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 assessment will be the VAS score at 6 hours after surgery.

Study contacts

Contact information is provided by the study sponsor or research team.

Beyza Çakır

CONTACT

[email protected]

+905372600955

Sponsors and collaborators

Lead sponsor

Ondokuz Mayıs University

Other

Registry information

Official study title

The Effect of Operating Room Orientation Video Education Applied at Different Times on Postoperative Pain and Anxiety in Patients Undergoing Prostate Surgery

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Aug 21, 2026
Registry last updated
Aug 21, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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