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Video-Based Preoperative Education in Laparoscopic Tubal Ligation

NCT07708974 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 80

Last updated 2026-07-16

No results posted yet for this study

Summary

This quasi-experimental study aimed to compare video-based preoperative education with traditional verbal counseling in terms of anxiety, postoperative pain, and patient satisfaction among women scheduled for laparoscopic tubal ligation. The study was conducted between January and June 2024 and included 80 women. Participants were allocated to either a routine verbal counseling group or a video-based education group, with 40 participants in each group. The video-based education group received preoperative counseling through an animated educational video, whereas the control group received routine verbal counseling. Demographic and obstetric characteristics were recorded. Anxiety levels were assessed using the Spielberger State-Trait Anxiety Inventory, postoperative pain was evaluated using the Visual Analogue Scale, and patient satisfaction was measured after the procedure. The outcomes of the two groups were compared to evaluate the effect of video-based preoperative education

Conditions

  • Patient Education
  • Tubal Ligation
  • Anxiety

Interventions

BEHAVIORAL

Video-Based Preoperative Education

Video-based preoperative education was provided to women before laparoscopic tubal ligation.

BEHAVIORAL

Routine Preoperative Information

Routine preoperative information was provided before laparoscopic tubal ligation as part of standard care.

Sponsors & Collaborators

  • Ordu University

    lead OTHER

Study Design

Allocation
NON_RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-01-01
Primary Completion
2024-06-30
Completion
2024-06-30

Countries

  • Turkey (Türkiye)

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07708974 on ClinicalTrials.gov