NCT07708974

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
80

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jan 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 30, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 30, 2024

Completed
2 years until next milestone

First Submitted

Initial submission to the registry

July 2, 2026

Completed
14 days until next milestone

First Posted

Study publicly available on registry

July 16, 2026

Completed
Last Updated

July 16, 2026

Status Verified

July 1, 2026

Enrollment Period

6 months

First QC Date

July 2, 2026

Last Update Submit

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

EXPERIMENTAL

Participants in this group received video-based preoperative education before laparoscopic tubal ligation.

Behavioral: Video-Based Preoperative Education

Routine Preoperative Information Group

ACTIVE COMPARATOR

Participants in this group received routine preoperative information before laparoscopic tubal ligation.

Behavioral: Routine Preoperative Information

Interventions

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

Video-Based Preoperative Education Group

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

Routine Preoperative Information Group

Eligibility Criteria

Age18 Years+
Sexfemale(Gender-based eligibility)
Gender Eligibility Detailsfemale
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Study Sites (1)

Ordu University

Ordu, Ordu, 52200, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Anxiety Disorders

Condition Hierarchy (Ancestors)

Mental Disorders

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.

Locations