MECLEES: Performance of EEG in Children With Medical Clowns

Sponsor
Bnai Zion Medical Center (Other)
Overall Status
Recruiting
CT.gov ID
NCT05257096
Collaborator
(none)
100
1
2
36
2.8

Study Details

Study Description

Brief Summary

EEG is an important test in the diagnosis epilepsy. The test does not hart, however many electrodes are attached to the child's scalp and situation is stressful. In order to achieve cooperation some use sedative drugs such as Chloralhydrate in young children. The investigetors believe that the integration of medical clowns in the EEG test can distract the children from the stressful environment and encourage them to cooperate. This can prevent the need of using sedation, can improve the quality of the test and improve the child's and parent's experience. One hundred children ages 1-10 years of age performing EEG test at the Bnai Zion medical center will be randomly divided into two groups. One group will the perform the test in the regular practice, and in the other half, medical clowns will be part of the test. The process will be rated by the child, his parents, the EEG technician and the physician reading the EEG. The two groups will be compared in all assessed measures through a statistical analysis.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Medical clown
N/A

Detailed Description

Can Medical Clowns prevent the usage of sedation during the performance of EEG in Young Children MECLEES - MEdical CLowns EEg Study

The study will be performed at the Pediatric Neurology Unit in Bnai Zion Medical Center, Haifa, Israel.

Purpose The aim our study is to investigate the performance of EEG in young children in cooperation with medical clowns. Can the presence of a medical clown prevent the need of using sedation? Does it improve the child's and parent's experience? Does it improve the quality of the test?

Study procedure The children will be divided to either group randomly according to the day of the test.

  1. 50 Children performing the EEG at the days that the medical clown is available will be included in the study group.

  2. 50 Children performing the EEG at the days that the medical clown is unavailable will be included in the control group.

Study group: The medical clown will meet the children in the waiting room for 15-30 minutes and will accompany them through the whole investigation, up to one hour.

Control group: children that will perform EEG without a medical clown, will perform it either with sedation or without one according to the common practice.

Outcome measures

The following parameters will be assessed (Appendix 1-4):
  1. Child anxiety using mYPAS (10-11) for assessing child anxiety questionnaire.

  2. Parent's satisfaction.

  3. Technician's evaluation.

  4. EEG quality will be evaluated by both technicians and the physicians independently. The physician will be blinded to the presence of a medical clown during the test.

Ethical consideration:

Prior to study ignition IRB approval will be obtained. Any change in the study protocol must be re-approved by the IRB.

All patients enrolled to the study must provide their written consent prior to entering the study. The informed consent will be signed by the parents and retained by the investigator as a part of the study records.

No records of names or identification will be published.

Statistical analysis The study will be randomized and controlled. The physician assessing the EEG will be blinded, however the child, his parents and the EEG technician's will not be blinded. Study and control groups will be compared via independent t-tests, significance will be considered if p<0.05.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
100 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
The children will be divided to either group randomly according to the day of the test. 50 Children performing the EEG at the days that the medical clown is available will be included in the study group. 50 Children performing the EEG at the days that the medical clown is unavailable will be included in the control group.The children will be divided to either group randomly according to the day of the test. 50 Children performing the EEG at the days that the medical clown is available will be included in the study group. 50 Children performing the EEG at the days that the medical clown is unavailable will be included in the control group.
Masking:
Single (Investigator)
Masking Description:
The EEG reading will be blinded to the intervention arm
Primary Purpose:
Prevention
Official Title:
Can Medical Clowns Prevent the Usage of Sedation During the Performance of EEG in Young Children
Actual Study Start Date :
May 1, 2019
Anticipated Primary Completion Date :
Apr 30, 2022
Anticipated Study Completion Date :
Apr 30, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Medical clown EEG

50 Children performing the EEG at the days that the medical clown is available will be included in the study group.

Behavioral: Medical clown
The medical clown will meet the children in the waiting room for 15-30 minutes and will accompany them through the whole investigation, up to one hour.
Other Names:
  • non
  • No Intervention: Regular EEG

    50 Children performing the EEG at the days that the medical clown is unavailable will be included in the control group. The EEG will be performed in the traditional way without medical clowns.

    Outcome Measures

    Primary Outcome Measures

    1. Anxiety [2 years]

      Child anxiety using the modified Yale Preoperative Anxiety Scale ( mYPAS 5-22 points, higher scores reflects anxity) for assessing child anxiety questionnaire.

    2. EEG quality [2 years]

      Electroencephalogram (EEG) quality will be evaluated by both technicians and the physicians independently in 1-5 likert sclae (1-best 5- worst). The physician will be blinded to the presence of a medical clown during the test.

    Secondary Outcome Measures

    1. Parent's satisfaction during EEG procedure [2 Years]

      Parent's satisfaction from the procedure on 1-5 likert sclae (1-best 5- worst).

    2. Technician's satisfaction during EEG procedure [2 Years]

      Technician's satisfaction from the procedure on 1-5 likert sclae (1-best 5- worst).

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    1 Month to 10 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No

    Inclusion Criteria

    • Children age 1-10 years

    • Undergoing EEG test at the Bnai Zion Medical Center.

    Exclusion Criteria

    • Children younger than 1 year or older than 10 years

    • Children using sedation for the test.

    • A child or a family that refuses to participate initially or during the test.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Bnai Zion Medical Center Haifa Israel 3104802

    Sponsors and Collaborators

    • Bnai Zion Medical Center

    Investigators

    • Principal Investigator: Jacob genizi, md, Bnai Zion Medical Center

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Jacob.genizi, Director Pediatric Departement, Bnai Zion Medical Center
    ClinicalTrials.gov Identifier:
    NCT05257096
    Other Study ID Numbers:
    • bnz 049-19
    First Posted:
    Feb 25, 2022
    Last Update Posted:
    Feb 25, 2022
    Last Verified:
    Feb 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Jacob.genizi, Director Pediatric Departement, Bnai Zion Medical Center
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Feb 25, 2022