Impact of Video-Based Patient Education on Physician Trust, Pain, and Anxiety in Laparoscopic Cholecystectomy

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorSanliurfa Education and Research Hospital

About this trial

This prospective, randomized, single-center, single-blind study aims to evaluate the effects of video-based preoperative education on physician trust, postoperative pain, anxiety, and opioid consumption in patients undergoing elective laparoscopic cholecystectomy under general anesthesia. Sixty-two ASA I-II patients aged 18-65 years will be randomized into two groups: standard verbal information alone or verbal information plus a standardized educational video regarding ultrasound-guided transversus abdominis plane (TAP) block. All patients will receive standardized general anesthesia, multimodal analgesia, and bilateral TAP block. The primary outcome will be physician trust assessed at postoperative 24 hours using the Trust in Physician Scale. Secondary outcomes include preoperative anxiety measured with the Amsterdam Preoperative Anxiety and Information Scale (APAIS), postoperative pain scores, opioid consumption, rescue analgesic requirement, and postoperative nausea and vomiting incidence. The study hypothesizes that video-based education will improve physician trust and perioperative patient-centered outcomes.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

18-65 years

American Society of Anesthesiologists (ASA) physical status I-II

Elective laparoscopic cholecystectomy

Disqualifiers

Psychiatric disease

Anticoagulant use or coagulopathy

Allergy to local anesthetic

Infection at the block site

Trial design

Design model

Parallel

Treatments tested in this trial

  • Video-Based Preoperative Block Education

    Behavioral

    Participants will receive standard preoperative verbal information plus a standardized educational video. The video demonstrates ultrasound anatomy and probe positioning for the transversus abdominis plane (TAP) block without showing invasive needle insertion or procedural performance. The content is designed to improve patient understanding of the regional anesthesia technique while maintaining procedural safety and standardization.

  • Standard Verbal Preoperative Block Education

    Behavioral

    Participants randomized to this group will receive standardized preoperative verbal education regarding the ultrasound-guided transversus abdominis plane (TAP) block. The explanation will be delivered by an anesthesiologist using a consistent script and will include the purpose of the block, expected analgesic benefits, and general procedural overview without the use of any visual, video, or multimedia materials. After preoperative education, all patients will undergo standardized general anesthesia, multimodal analgesia, and bilateral ultrasound-guided TAP block as part of routine perioperative care.

Treatment groups

62 Participants
are divided into 2 treatment groups
Group A: Standard Verbal Information GroupActive comparator 1 intervention
Group B: Video-Based Education GroupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Trust in Physician

Physician trust will be assessed using the Trust in Physician Scale. The scale evaluates patients' trust in their treating physician regarding communication, competence, and reliability. Higher scores indicate greater trust in the physician.

Time frame
Twenty-four hours after surgery

Secondary outcomes

1

Postoperative Pain

Postoperative pain will be assessed using the Numeric Rating Scale ranging from zero to ten, where zero indicates no pain and ten indicates the worst imaginable pain. Pain scores will be recorded at predefined postoperative time points.

Time frame
Immediately after surgery, four hours after surgery, twelve hours after surgery, and twenty-four hours after surgery
2

Preoperative Anxiety

Preoperative anxiety will be measured using the Amsterdam Preoperative Anxiety and Information Scale (APAIS). This validated questionnaire assesses anxiety levels and information requirement related to surgery and anesthesia. The scale will be used to evaluate the effect of preoperative educational intervention (standard verbal information or video-based education) on patient anxiety levels.

Time frame
After completion of preoperative education intervention and approximately one hour before surgery
3

Total Opioid Consumption

Total postoperative opioid consumption will be recorded and converted to intravenous morphine equivalent doses for standardization across patients.

Time frame
First twenty-four hours after surgery
4

Postoperative Nausea and Vomiting Incidence

Incidence of postoperative nausea and vomiting will be recorded based on patient reports and clinical observation, including any need for antiemetic treatment.

Time frame
First twenty-four hours after surgery

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.