CClinicalTrials.gg
CompletedNCT07097636Video EducatioUpdated Jul 31, 2025

Effect of Video Education on Anxiety and Satisfaction Levels of Parents of Children Undergoing Urodynamic Studies

An interventional study of Video education and No intervention in Anxiety and Satisfaction, sponsored by Eskisehir Osmangazi University. Completed at 1 site in Turkey (Türkiye). Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-07-31.

Sponsored by Eskisehir Osmangazi University · Not applicable, Interventional, and Other

From the registry’s dates

  • Registered 2 years after the study started (first participant enrolled Jul 2023, registered Jul 2025).
Phase
Not applicable
Study type
Interventional
Enrollment
140
Allocation
Randomized
Ages
18 Years and older
Sex
All
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Study summary

The aim of this study was to evaluate the effects of video-based education provided to parents of children undergoing urodynamic testing on their State-Trait Anxiety Inventory and satisfaction levels. While some of the parents of children scheduled for urodynamic testing were shown a video, others were not. Anxiety and satisfaction levels were assessed in both groups before and after the procedure.

Read the detailed description

This study was conducted at Bursa Yuksek Ihtisas Training and Research Hospital between July 2023 and January 2024 to evaluate the effect of video-based education provided to parents of children undergoing urodynamic testing on their anxiety and satisfaction levels. Participants were randomly assigned to two groups. In the control group, parents received information about the urodynamic procedure from the nurses performing the test. In the intervention group, in addition to receiving information, the parents were shown a video explaining the urodynamic procedure. All questions from the participants were answered by the nurse conducting the urodynamic procedure. A total of 140 patients were planned to be included in the study, with 70 in each group. The State-Trait Anxiety Inventory (STAI) was used to assess anxiety levels, and a verbal descriptive scale was used to evaluate satisfaction with the procedure.

02

Conditions studied

  • Anxiety
  • Satisfaction
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In context

Anxiety Disorders

4,868 studies on the registry are indexed under Anxiety Disorders; 1,390 are open to participants now.

This study's enrollment of 140 is above the median of 80 across 4,174 interventional studies indexed under Anxiety Disorders.

Browse Anxiety Disorders studies →

Lead sponsor

Eskisehir Osmangazi University is the lead sponsor of 149 studies on the registry; 27 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Eligibility criteria

Inclusion Criteria:Parents must be at least 18 years old,

  • Parents must be at least 18 years old
  • have no intellectual disabilities or perception problems
  • have no communication difficulties.

Exclusion Criteria

  • Insufficient proficiency in Turkish and unwillingness to participate in the study
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Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Investigator)
Enrollment
140 participants (actual)

Study arms

  • Experimental
    İntervention

    Video education

    Other: Video education

  • Other
    No intervention

    Control group

    Other: No intervention

Interventions

  • OtherVideo education

    A video demonstrating the steps of the urodynamic procedure was shown, and afterward, participants' questions were answered by an experienced nurse who performed the procedure.

    Also known as: İntervention group

  • OtherNo intervention

    Children scheduled to undergo urodynamic testing for any reason received the procedure without any prior video-based education being provided to their parents

    Also known as: Control group

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What researchers measure

Primary outcomes

  1. Parents' anxiety levels before the education

    Anxiety levels before the procedure will be assessed using the State-Trait Anxiety Inventory, which consists of 20 questions. Each question is scored from 1 to 4. A total score below 30 indicates low anxiety, a score between 31 and 45 indicates moderate anxiety, and a score of 46 or above indicates high anxiety. The urodynamic procedure will be performed according to routine clinical practice. High scores indicate high anxiety, while low scores indicate low anxiety.

    Time frame: Immediately before procedurel]

  2. Parents' anxiety levels after the education

    Parents in the control group will receive only verbal information, while parents in the study group will be given verbal education as well as shown a video. After the education, the anxiety levels of the parents will be assessed using the State-Trait Anxiety Inventory - State (STAI-S).

    Time frame: Immediately after education

Secondary outcomes

  1. Parental satisfaction levels regarding the video training

    The satisfaction levels of parents in the intervention group after the video training were evaluated using a verbal descriptive scale. This scale is rated as follows: I) Not satisfied at all II) Not satisfied III) Neither satisfied nor dissatisfied IV) Satisfied V) Very satisfied High scores indicate high satisfaction, while low scores indicate low satisfaction.

    Time frame: Immediately after the education

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Study locations

1 site
  • Bursa Yüksek İhtisas Training and Research Hospital
    Bursa, Turkey (Türkiye)
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References and documents

Individual participant data

Plan to share: Yes

Supporting information: Study protocol

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 31, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07097636
Lead sponsor
Eskisehir Osmangazi University
Responsible party
Rüya Naz (Principal Investigator, Eskisehir Osmangazi University) — Principal investigator
First posted
Jul 31, 2025
Start date
Jul 5, 2023
Primary completion
Jan 5, 2024
Completion
Jan 5, 2024
Last update
Jul 31, 2025

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jul 2025. You cannot join it, but the record below documents what was studied.

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