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Evaluation of the Effects of LUNII on Pre-operative Anxiety and on the Post-operative Period in Children With Cleft Lip and Palate Admitted for Alveolar Bone Graft: Pilot Study

Evaluation of the Effects of LUNII on Pre-operative Anxiety and on the Post-operative Period in Children With Cleft Lip and Palate Admitted for Alveolar Bone Graft: Pilot Study

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03740841
Acronym
LUNII
Enrollment
15
Registered
2018-11-14
Start date
2019-01-08
Completion date
2019-01-08
Last updated
2025-09-25

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

Conditions

Cleft Lip and Palate

Keywords

Per-operative stress, per-operative anxiety, pediatric surgery

Brief summary

The literature on the effects of various devices on per-operative anxiety is scarce. There is currently no study on the effects of an interactive storyteller on per-operative anxiety in pediatric surgery. The interactive story teller LUNII (available over the counter in France) would reduce pre-operative anxiety, with post-operative effects on pain and hospitalization time.

Detailed description

The literature on the effects of various devices on per-operative anxiety is scarce. There is currently no study on the effects of an interactive storyteller on per-operative anxiety in pediatric surgery. The interactive story teller LUNII (available over the counter in France) would reduce pre-operative anxiety, with post-operative effects on pain and hospitalization time. Patients admitted for an alveolar bone graft with an iliac donor site as part of the treatment of their cleft lip and palate will be include for two reasons: 1. It is a homogeneous population - same condition, same treatment, same age at surgery, standardized procedure; 2. It is a population with long individual medical histories and, potentially, subjected to significant surgery-related stress. Patients will be randomized into two groups: with LUNII and without LUNII. In the LUNII group, the interactive story teller LUNII will be delivered the day before surgery during the pre-operative medical visit.

Interventions

BEHAVIORALInteractive story teller LUNII

Use of the interactive story teller LUNII by the child from the pre-operative visit to the discharge.

Sponsors

URC-CIC Paris Descartes Necker Cochin
CollaboratorOTHER
Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
4 Years to 6 Years
Healthy volunteers
No

Inclusion criteria

* Children aged 4 to 6 years. * Alveolar bone graft with iliac crest donor site in children with unilateral or bilateral cleft lip and palate * Primary alveolar bone graft or first side when bilateral cleft * Followed at Necker since birth and operated according to the protocol used in the department. * Consent signed by the holder (or holders) of parental authority

Exclusion criteria

* Medical care different from the usual protocol applied in the service (secondary surgery, age \> 7 years) * Known psychomotor delay, associated rare syndrome or disease, known psychiatric disorders, other surgical procedures between hard palate closure and alveolar bone graft * Possession and/or prior use of LUNII by the child

Design outcomes

Primary

MeasureTime frameDescription
Yale Preoperative Anxiety Scale (mYPAS )At the entrance into the operating roomQuestionnaire, completed in the operating room by an independent observer preferably without knowledge about the child, made of 22 items divided into 5 categories. The score ranges from 5 (minimum anxiety) to 20 (maximum anxiety)
Number of hours spent with the interactive story teller LUNII before surgeryDay of surgery (D0)Number of hours spent with the interactive story teller LUNII

Secondary

MeasureTime frameDescription
Analgesic administrationUp to 1 weekEvaluation of analgesic administration after surgery during hospital stay
Visual Analogue pain Scale (EVA)Up to 1 weekSelf-assessment of pain by a graduated ruler of 0 (no pain) at 100 millimeters (maximum pain imaginable), twice a day during hospitalization
Duration between the operation and the first surveyUp to 1 weekDuration between the operation and the first survey
Length of hospitalizationUp to 1 weekLength of hospitalization

Countries

France

Outcome results

None listed

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