Patient EducationVPE-LTLNCT07708974
Video-Based Preoperative Education in Laparoscopic Tubal Ligation
A study testing Video-Based Preoperative Education and Routine Preoperative Information in people with Patient Education and Tubal Ligation, run by Ordu University at 1 site in Turkey (Türkiye).
Trial 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. Read more about this study
- Who is it for?
- Ages 18 years and older, women only
- Conditions the study is for
- Patient Education, Tubal Ligation, Anxiety
- What is being tested?
- Video-Based Preoperative Education and Routine Preoperative Information
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 80 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 1 Jan 2024to 30 Jun 2024
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- Women only
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- 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
Who cannot join
- 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
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Video-Based Preoperative Education Versus Traditional Verbal Counseling for Anxiety, Pain, and Patient Satisfaction in Women Undergoing Laparoscopic Tubal Ligation: A Quasi-Experimental Study
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
- Being tested
- Video-Based Preoperative Education, Routine Preoperative Information
- Medical subject headings
- Anxiety Disorders
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Video-Based Preoperative EducationBehavioural
Video-based preoperative education was provided to women before laparoscopic tubal ligation.
Routine Preoperative InformationBehavioural
Routine preoperative information was provided before laparoscopic tubal ligation as part of standard care.
| Study group | Role | What they receive |
|---|---|---|
| Video-Based Preoperative Education Group | Experimental | Participants in this group received video-based preoperative education before laparoscopic tubal ligation. Receives: Behavioral: Video-Based Preoperative Education |
| Routine Preoperative Information Group | Active comparator | Participants in this group received routine preoperative information before laparoscopic tubal ligation. Receives: Behavioral: Routine Preoperative Information |
What is being measured
The primary outcome is the main question the study is designed to answer.
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
Measured: Immediately after recovery from anesthesia on the day of surgery
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted16 Jul 2026
- Study start1 Jan 2024
- Primary completion30 Jun 2024
- Study completion30 Jun 2024
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Patient EducationStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Supportive care
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 80 participants (actual)
Sponsor and investigators
- Lead sponsor
- Ordu University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, burcu özata, Ordu University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07708974
- Sponsor's protocol ID
- LTL-VPE-2024-001
- Acronym
- VPE-LTL
- Status last verified
- Jul 2026
- First submitted
- 2 Jul 2026
- Last updated
- 16 Jul 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: Individual participant data will not be shared.
Study at a glance
From the registry record, last updated by the sponsor on 16 Jul 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Video-Based Preoperative Education Versus Traditional Verbal Counseling for Anxiety, Pain, and Patient Satisfaction in Women Undergoing Laparoscopic Tubal Ligation: A Quasi-Experimental Study
- ClinicalTrials.gov ID
- NCT07708974
- Acronym / sponsor ID
- VPE-LTL / LTL-VPE-2024-001
- Conditions
- Patient Education, Tubal Ligation, Anxiety
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 80 participants (actual)
- Lead sponsor
- Ordu UniversityUniversity, hospital or other
- Study start
- 1 Jan 2024 (actual)
- Primary completion
- 30 Jun 2024 (actual)
- Study completion
- 30 Jun 2024 (actual)
- First posted
- 16 Jul 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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
Study design
- Primary purpose
- Supportive care
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Video-Based Preoperative Education Group | Experimental | Behavioral: Video-Based Preoperative EducationParticipants in this group received video-based preoperative education before laparoscopic tubal ligation. |
| Routine Preoperative Information Group | Active comparator | Behavioral: Routine Preoperative InformationParticipants in this group received routine preoperative information before laparoscopic tubal ligation. |
Who may qualify
- Ages
- 18 years and older
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (1 listed)
- 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
Key exclusion criteria (1 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Video-Based Preoperative EducationVideo-based preoperative education was provided to women before laparoscopic tubal ligation. | Behavioural | Video-Based Preoperative Education Group |
| Routine Preoperative InformationRoutine preoperative information was provided before laparoscopic tubal ligation as part of standard care. | Behavioural | Routine Preoperative Information Group |
Primary outcome
Mean Postoperative Patient Satisfaction Score on a Single-Item 5-Point Likert Satisfaction Scale
Time frame: Immediately after recovery from anesthesia on the day of surgery
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
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 16 Jul 2026.
- Individual participant dataSharing planned: No. Individual participant data will not be shared.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Video-Based Preoperative Education and Routine Preoperative Information in people with Patient Education and Tubal Ligation, run by Ordu University at 1 site in Turkey (Türkiye).
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 16 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Mean Postoperative Patient Satisfaction Score on a Single-Item 5-Point Likert Satisfaction Scale (time frame: Immediately after recovery from anesthesia on the day of surgery). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 16 Jul 2026.