Video-Based Preoperative Education in Laparoscopic Tubal Ligation
VPE-LTL
1 other identifier
interventional
80
1 country
1
Brief 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
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Jan 2024
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 30, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
June 30, 2024
CompletedFirst Submitted
Initial submission to the registry
July 2, 2026
CompletedFirst Posted
Study publicly available on registry
July 16, 2026
CompletedJuly 16, 2026
July 1, 2026
6 months
July 2, 2026
July 11, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Mean Postoperative Patient Satisfaction Score on a Single-Item 5-Point Likert Satisfaction Scale
Overall postoperative patient satisfaction was assessed using a single-item 5-point Likert satisfaction scale. Participants selected one response ranging from 1 point ("not satisfied at all") to 5 points ("very satisfied"). The unit of measure is points. Higher scores indicate greater patient satisfaction. The outcome metric is the mean satisfaction score reported for each study arm
Immediately after recovery from anesthesia on the day of surgery
Study Arms (2)
Video-Based Preoperative Education Group
EXPERIMENTALParticipants in this group received video-based preoperative education before laparoscopic tubal ligation.
Routine Preoperative Information Group
ACTIVE COMPARATORParticipants in this group received routine preoperative information before laparoscopic tubal ligation.
Interventions
Video-based preoperative education was provided to women before laparoscopic tubal ligation.
Routine preoperative information was provided before laparoscopic tubal ligation as part of standard care.
Eligibility Criteria
You may qualify if:
- Women who voluntarily agreed to participate in the study Women scheduled for laparoscopic tubal ligation and deemed medically eligible for surgery Women who were able to provide informed consent For participants assigned to the video-based education group, sufficient visual and auditory ability to watch and understand the educational video
You may not qualify if:
- Women who declined to participate Women who were unable to read and understand the study materials Women with conditions that prevented reliable completion of the study assessments Women who did not complete the required assessment forms
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Ordu Universitylead
Study Sites (1)
Ordu University
Ordu, Ordu, 52200, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
July 2, 2026
First Posted
July 16, 2026
Study Start
January 1, 2024
Primary Completion
June 30, 2024
Study Completion
June 30, 2024
Last Updated
July 16, 2026
Record last verified: 2026-07
Data Sharing
- IPD Sharing
- Will not share
Individual participant data will not be shared.