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Tablet-based Interactive Distraction Preoperative Anxiety in Children: A Randomized Controlled Trial

Tablet-based Interactive Distraction for the Management of Preoperative Anxiety in Children: A Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03531359
Acronym
TABLET
Enrollment
112
Registered
2018-05-21
Start date
2018-07-04
Completion date
2020-07-30
Last updated
2018-09-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Children Under General Anaesthesia

Brief summary

Children develop anxiety during the induction of anaesthesia and video-games might reduce or alleviate it. The investigators intend to conduct a clinical trial to study the effect of tablet-based interctive games on alleviating preoperative anxiety.

Detailed description

It is estimated that 50% of children may suffer preoperative anxiety. They have a higher risk of generating postanesthetic delirium and behavioral changes in the postoperative period up to 67% of cases. For the management of preoperative anxiety there are pharmacological and non-pharmacological treatments. Within the first group there's the use of benzodiazepines of short half life like midazolam, however, the use of this medication is not exempt of risks such as paradox reactions, respiratory depression, among others. This is why the non pharmacological mesures have taken force and every day there is more evidence regarding its effectiveness. There are no reports in Chile or latin america regarding the use of this tools, this is why the investigators designed this study to prove the effectiveness of audiovisual distraction measures in reducing preparatory anxiety compared to premeditation with midazolam.

Interventions

DEVICETIBD

Table-based Interactive Distraction using video-games will be used to prove efficacy in preventing preoperative anxiety.

DRUGMidazolam

Administration of midazolam oral or rectal 30 minutes to one hour prior to transfer to the theater.

Sponsors

Hospital Carlos Van Buren
CollaboratorOTHER
Universidad de Valparaiso
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

Anxiety will be determined by using a video recording of the child, which will be assessed by psychiatric

Intervention model description

Tablet Group: They'll receive a tablet with content adapted to every group. It will be divided into 4 groups (2-4 years, 4-6 years, 6-8 years and 9-10 years). The first one will receive cartoons, the second will also have games; for the other two groups will be assigned appropriate video games depending on the age. Midazolam group: They'll receive 0,5mg/kg oral or it's equivalent in rectal administration 30 minutes to one hour prior to transfer to the theater. This patients will not be able to have contact with audiovisual devices.

Eligibility

Sex/Gender
ALL
Age
2 Years to 10 Years
Healthy volunteers
No

Inclusion criteria

Children aged 2-10 years, under major surgery ambulatory program at Hospital Carlos Van Buren, with no contraindication for the use of midazolam.

Exclusion criteria

Patients with cognitive impairment or sensory deficit Patients with previous history of major surgery will also be excluded Patients with myastenia Hard airway History of paroxystic reaction to benzodiazepines Attentional deficit hyperactivity disorder Sleep aphnea Full stomach Adenotonsillar hypertrophy Respiratory acute infections

Design outcomes

Primary

MeasureTime frameDescription
Short version of the modified Yale Preoperative Anxiety Scale(mYPAS-SF)6 hoursDifference between the measurement of the mYPAS-SF applied in the preoperative time and prior to induction. The scale has 18 items in 4 categories. Maximum score is 100 points. The higher the score, the greater the anxiety.

Secondary

MeasureTime frameDescription
Cooperation with the induction30 minutsScale with 10 items, 1 point for each one. 0 points shows an induction with perfect cooperation. This scale will be applied at the moment of the induction by the anesthesiologist
Changes in postoperative behavior10 daysThe Post Behavioral Behavior Change Questionnaire (PHBQ) will be applied at the postoperative surgical control (7-10 days after the intervention). This survey will be applied by people trained by the hospital's pediatric psychiatry team The higher the score, the more behavioral changes in the postoperative period
Emergence delirium1 hourIn the post-anesthesia recovery unit, the Emergency Delirium Scale for Pediatric Anesthesia (PAED) will be applied every 15 minutes during the first 30 minutes of their stay in the unit. Score goes from 0 to 20. Scores greater than 10 is considered as delirium.
Parents Satisfaction10 minutsA gradual scale will be applied to the parents of the patient upon discharge from hospital.

Countries

Chile

Contacts

Primary ContactNathalie López, MD
nathalielopez.jq@gmail.com2364000
Backup ContactAnamaria Correa, MD
anamaria.correa@uv.cl2364000

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026