NCT07767344 Impact of Video-Based Patient Education on Physician Trust, Pain, and Anxiety in Laparoscopic Cholecystectomy
| NCT ID | NCT07767344 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Sanliurfa Education and Research Hospital |
| Condition | Postoperative Pain |
| Study Type | INTERVENTIONAL |
| Enrollment | 62 participants |
| Start Date | 2026-08-12 |
| Primary Completion | 2026-10-12 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 62 participants in total. It began in 2026-08-12 with a primary completion date of 2026-10-12.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
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
Inclusion Criteria: * 18-65 years * American Society of Anesthesiologists (ASA) physical status I-II * Elective laparoscopic cholecystectomy Exclusion Criteria: * Psychiatric disease * Anticoagulant use or coagulopathy * Allergy to local anesthetic * Infection at the block site * Thoracic deformity * Inability to comprehend pain or anxiety assessment scales.
Contact & Investigator
Frequently Asked Questions
Who can join the NCT07767344 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, up to 65 Years, studying Postoperative Pain. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07767344 currently recruiting?
Yes, NCT07767344 is actively recruiting participants. Contact the research team at tkaracay35@gmail.com for enrollment information.
Where is the NCT07767344 trial being conducted?
This trial is being conducted at Sanliurfa, Turkey (Türkiye).
Who is sponsoring the NCT07767344 clinical trial?
NCT07767344 is sponsored by Sanliurfa Education and Research Hospital. The trial plans to enroll 62 participants.