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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 (LUNII)

Primary Purpose

Cleft Lip and Palate

Status
Terminated
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Interactive story teller LUNII
Sponsored by
Assistance Publique - Hôpitaux de Paris
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Cleft Lip and Palate focused on measuring Per-operative stress, per-operative anxiety, pediatric surgery

Eligibility Criteria

4 Years - 6 Years (Child)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Hôpital Necker-Enfants Malades

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

No Intervention

Arm Label

LUNII

Without LUNII

Arm Description

The interactive story teller LUNII is delivered to the child the day before surgery, during the usual pre-operative medical visit.

Usual pre-operative visit.

Outcomes

Primary Outcome Measures

Yale Preoperative Anxiety Scale (mYPAS )
Questionnaire, 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)
Yale Preoperative Anxiety Scale (mYPAS )
Questionnaire, 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 surgery
Number of hours spent with the interactive story teller LUNII

Secondary Outcome Measures

Analgesic administration
Evaluation of analgesic administration after surgery during hospital stay
Visual Analogue pain Scale (EVA)
Self-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 survey
Duration between the operation and the first survey
Length of hospitalization
Length of hospitalization

Full Information

First Posted
November 2, 2018
Last Updated
March 21, 2022
Sponsor
Assistance Publique - Hôpitaux de Paris
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1. Study Identification

Unique Protocol Identification Number
NCT03740841
Brief Title
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
Acronym
LUNII
Official Title
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
Study Type
Interventional

2. Study Status

Record Verification Date
March 2022
Overall Recruitment Status
Terminated
Why Stopped
Unsuccessful study
Study Start Date
January 8, 2019 (Actual)
Primary Completion Date
January 8, 2019 (Actual)
Study Completion Date
January 8, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

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: It is a homogeneous population - same condition, same treatment, same age at surgery, standardized procedure; 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cleft Lip and Palate
Keywords
Per-operative stress, per-operative anxiety, pediatric surgery

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
15 (Actual)

8. Arms, Groups, and Interventions

Arm Title
LUNII
Arm Type
Other
Arm Description
The interactive story teller LUNII is delivered to the child the day before surgery, during the usual pre-operative medical visit.
Arm Title
Without LUNII
Arm Type
No Intervention
Arm Description
Usual pre-operative visit.
Intervention Type
Behavioral
Intervention Name(s)
Interactive story teller LUNII
Intervention Description
Use of the interactive story teller LUNII by the child from the pre-operative visit to the discharge.
Primary Outcome Measure Information:
Title
Yale Preoperative Anxiety Scale (mYPAS )
Description
Questionnaire, 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)
Time Frame
At the entrance into the operating room
Title
Yale Preoperative Anxiety Scale (mYPAS )
Description
Questionnaire, 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)
Time Frame
At the time of anesthetic induction
Title
Number of hours spent with the interactive story teller LUNII before surgery
Description
Number of hours spent with the interactive story teller LUNII
Time Frame
Day of surgery (D0)
Secondary Outcome Measure Information:
Title
Analgesic administration
Description
Evaluation of analgesic administration after surgery during hospital stay
Time Frame
Up to 1 week
Title
Visual Analogue pain Scale (EVA)
Description
Self-assessment of pain by a graduated ruler of 0 (no pain) at 100 millimeters (maximum pain imaginable), twice a day during hospitalization
Time Frame
Up to 1 week
Title
Duration between the operation and the first survey
Description
Duration between the operation and the first survey
Time Frame
Up to 1 week
Title
Length of hospitalization
Description
Length of hospitalization
Time Frame
Up to 1 week

10. Eligibility

Sex
All
Minimum Age & Unit of Time
4 Years
Maximum Age & Unit of Time
6 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Roman Hossein Khonsari, MD, PhD
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hôpital Necker-Enfants Malades
City
Paris
ZIP/Postal Code
75015
Country
France

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

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

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