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Use of a Connected Companion in Children With Cystic Fibrosis (COMPANION-CF)

Primary Purpose

Cystic Fibrosis in Children, Chronic Disease

Status
Unknown status
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Connected device named "Leo" from Ludocare society
Sponsored by
Centre Hospitalier de Saint-Brieuc
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Cystic Fibrosis in Children focused on measuring Connected device, Long-term therapy, Pneumology, Adherence therapy, Pediatric research, Pediatric device support

Eligibility Criteria

3 Years - 11 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Child volunteer from 3 to 11 years old
  • Affected by cystic fibrosis
  • With a prescription containing at least two medications twice a day
  • Affiliation to the national health insurance
  • Child and holder of the exercise of parental authority understands and speaks French
  • The person exercising parental authority must have reached the age of majority.
  • Collection of the written consent of one of the holders of the exercise of parental authority

Exclusion Criteria:

  • Non-voluntary child, under 3 years of age or over 12 years of age
  • Family reluctant to technology
  • Family without smartphone and/or wifi connection
  • Failure to obtain the written consent of one of the holders of the exercise of parental authority
  • Child involved in research involving the human person

Sites / Locations

  • Chu Rennes
  • Centre Hospitalier de Saint-BrieucRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Connected device

Arm Description

Connected device for three months period to support children care

Outcomes

Primary Outcome Measures

Evaluate therapeutic adherence of children with cystic fibrosis aged 3 to 11 years with help of a connected medical companion
The main evaluation criterion will be the overall compliance of the cohort in percentage terms. These data from connected companion will be refined for each type of treatment: pancreatic extracts, inhaled treatments, CFTR modulator, antibiotics, vitamins, laxative treatment, antacids, bile acids, food supplements, physiotherapy. For each treatment, the data "take" or "not take" will be treated by device and provide for statistical analysis in percentage. Each percentage will be grouped in global percentage will be therapeutic adherence all over study.

Secondary Outcome Measures

Study of the reasons of low compliance or difficulties in taking the treatments
Questionnaire for parents with up to 15 treatments which provide the major difficulties (to be indicated in order, from the most difficult to the simplest, with checked answers; no specific scale available)
Assess the psycho-social impact of treatment and illness
Questionnaire for parents on child's behaviours in regard to taking treatment and illness (scale from 0 to 10, , highers scores mean better outcome)
Assess child's autonomy regarding his treatments
Reporting in connected device
Assess the intake treatments quality
Questionnaire for parents on difficulties frequency with checked answers (no specific scale available)
Evaluate any negative impacts associated with the use of the robot
Questionnaire for parents on difficulties linked to the use of the robot with scale from 0 to 10, highers scores mean better outcome, and open ended questions (no specific scale is available)
Evaluate any negative impacts associated with the use of the robot
Questionnaire for parents on difficulties linked to the use of the robot with scale from 0 to 10, highers scores mean better outcome, and open ended questions (no specific scale is available)
Assess the psycho-social impact of treatment and illness
Questionnaire for children on his relation to his illness and his treatments (Color gradient scale with expressive smiley : red (sad), orange (a little bit sad), yellow (neutral), light green (good), dark green (very good)
Assess the psycho-social impact of treatment and illness
Questionnaire for children on his relation to his illness and his treatments (Color gradient scale with expressive smiley : red (sad), orange (a little bit sad), yellow (neutral), light green (good), dark green(very good)
Assess the psycho-social impact of treatment and illness
Questionnaire for children on his relation to his illness and his treatments (Color gradient scale with expressive smiley : red (sad), orange (a little bit sad), yellow (neutral), light green (good), dark green(very good)
Study of the reasons of low compliance or difficulties in taking the treatments
Questionnaire for parents with up to 15 treatments which provide the major difficulties (to be indicated in order, from the most difficult to the simplest, with checked answers; no specific scale available)
Assess the psycho-social impact of treatment and illness
Questionnaire for parents on child's behaviours in regard to taking treatment and illness (scale from 0 to 10, , highers scores mean better outcome)
Assess the intake treatments quality
Questionnaire for parents on difficulties frequency with checked answers (no specific scale available)
Study of the reasons of low compliance or difficulties in taking the treatments
Questionnaire for parents with up to 15 treatments which provide the major difficulties (to be indicated in order, from the most difficult to the simplest, with checked answers; no specific scale available)
Assess the psycho-social impact of treatment and illness
Questionnaire for parents on child's behaviours in regard to taking treatment and illness (scale from 0 to 10, , highers scores mean better outcome)
Assess child's autonomy regarding his treatments
Reporting in connected device
Assess the intake treatments quality
Questionnaire for parents on difficulties frequency with checked answers (no specific scale available)

Full Information

First Posted
December 14, 2020
Last Updated
January 20, 2021
Sponsor
Centre Hospitalier de Saint-Brieuc
Collaborators
Rennes University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT04705636
Brief Title
Use of a Connected Companion in Children With Cystic Fibrosis
Acronym
COMPANION-CF
Official Title
Use of a Connected Companion in Children With Cystic Fibrosis - COMPANION-CF
Study Type
Interventional

2. Study Status

Record Verification Date
January 2021
Overall Recruitment Status
Unknown status
Study Start Date
January 20, 2021 (Actual)
Primary Completion Date
June 2021 (Anticipated)
Study Completion Date
June 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Hospitalier de Saint-Brieuc
Collaborators
Rennes University Hospital

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 study will be conducted over a 6 months period. For the first three months, the child will be accompagned with a connected companion. After this period, the companion will be removed for three months in oder to prove this companion could improve treatment adherence for children suffering from cytolisis fibrosis. This study will be conducted at the University Hospital Center of Rennes and Hospital Center of Saint-Brieuc.
Detailed Description
In developed countries, chronic diseases with long-term therapy adherence is about 50%, according to the WHO report, and the adherence rate for regular intake of preventive therapies decreases to 28%. For cystic fibrosis, rates are not much higher. Optimistic articles report an average compliance rate of 60%. Other articles report a rate of 50% which varies according to the age of the patient, the intake treatment complexity and burdensome drug treatment (physiotherapy achieves the lowest adherence with 38%), the disease understanding and the interest of treatment persuasion. Low adherence can also be the result of incorrect use of administration devices, for example for inhaled treatments. Technical errors are very frequent and affect around 30% of patients. Families with children suffering from cystic fibrosis need daily support. Health professionals need to relay their recommendations at home. This is why new and funny tools dedicated to children with chronic illnesses are needed. This trial will study the impact of connected companion named LEO® created by Ludocare company. Study will be conducted as : V0 : Companion given to the child V1 : Companion removed after 3 months of use V2 : Follow-up done between 1 and 3 months after the period without companion

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cystic Fibrosis in Children, Chronic Disease
Keywords
Connected device, Long-term therapy, Pneumology, Adherence therapy, Pediatric research, Pediatric device support

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Connected device
Arm Type
Experimental
Arm Description
Connected device for three months period to support children care
Intervention Type
Device
Intervention Name(s)
Connected device named "Leo" from Ludocare society
Intervention Description
Connected device named "Leo" from Ludocare society will be allocated to each child for three-months period. During this time, child will be helped to take all of his medication and specific care by this connected device.
Primary Outcome Measure Information:
Title
Evaluate therapeutic adherence of children with cystic fibrosis aged 3 to 11 years with help of a connected medical companion
Description
The main evaluation criterion will be the overall compliance of the cohort in percentage terms. These data from connected companion will be refined for each type of treatment: pancreatic extracts, inhaled treatments, CFTR modulator, antibiotics, vitamins, laxative treatment, antacids, bile acids, food supplements, physiotherapy. For each treatment, the data "take" or "not take" will be treated by device and provide for statistical analysis in percentage. Each percentage will be grouped in global percentage will be therapeutic adherence all over study.
Time Frame
Through study completion, up to 6 months
Secondary Outcome Measure Information:
Title
Study of the reasons of low compliance or difficulties in taking the treatments
Description
Questionnaire for parents with up to 15 treatments which provide the major difficulties (to be indicated in order, from the most difficult to the simplest, with checked answers; no specific scale available)
Time Frame
At the inclusion
Title
Assess the psycho-social impact of treatment and illness
Description
Questionnaire for parents on child's behaviours in regard to taking treatment and illness (scale from 0 to 10, , highers scores mean better outcome)
Time Frame
At the inclusion
Title
Assess child's autonomy regarding his treatments
Description
Reporting in connected device
Time Frame
3 months
Title
Assess the intake treatments quality
Description
Questionnaire for parents on difficulties frequency with checked answers (no specific scale available)
Time Frame
At the inclusion
Title
Evaluate any negative impacts associated with the use of the robot
Description
Questionnaire for parents on difficulties linked to the use of the robot with scale from 0 to 10, highers scores mean better outcome, and open ended questions (no specific scale is available)
Time Frame
3 months
Title
Evaluate any negative impacts associated with the use of the robot
Description
Questionnaire for parents on difficulties linked to the use of the robot with scale from 0 to 10, highers scores mean better outcome, and open ended questions (no specific scale is available)
Time Frame
4 to 6 months
Title
Assess the psycho-social impact of treatment and illness
Description
Questionnaire for children on his relation to his illness and his treatments (Color gradient scale with expressive smiley : red (sad), orange (a little bit sad), yellow (neutral), light green (good), dark green (very good)
Time Frame
at the inclusion
Title
Assess the psycho-social impact of treatment and illness
Description
Questionnaire for children on his relation to his illness and his treatments (Color gradient scale with expressive smiley : red (sad), orange (a little bit sad), yellow (neutral), light green (good), dark green(very good)
Time Frame
3 months
Title
Assess the psycho-social impact of treatment and illness
Description
Questionnaire for children on his relation to his illness and his treatments (Color gradient scale with expressive smiley : red (sad), orange (a little bit sad), yellow (neutral), light green (good), dark green(very good)
Time Frame
4 to 6 months
Title
Study of the reasons of low compliance or difficulties in taking the treatments
Description
Questionnaire for parents with up to 15 treatments which provide the major difficulties (to be indicated in order, from the most difficult to the simplest, with checked answers; no specific scale available)
Time Frame
3 months
Title
Assess the psycho-social impact of treatment and illness
Description
Questionnaire for parents on child's behaviours in regard to taking treatment and illness (scale from 0 to 10, , highers scores mean better outcome)
Time Frame
3 months
Title
Assess the intake treatments quality
Description
Questionnaire for parents on difficulties frequency with checked answers (no specific scale available)
Time Frame
3 months
Title
Study of the reasons of low compliance or difficulties in taking the treatments
Description
Questionnaire for parents with up to 15 treatments which provide the major difficulties (to be indicated in order, from the most difficult to the simplest, with checked answers; no specific scale available)
Time Frame
4 to 6 months
Title
Assess the psycho-social impact of treatment and illness
Description
Questionnaire for parents on child's behaviours in regard to taking treatment and illness (scale from 0 to 10, , highers scores mean better outcome)
Time Frame
4 to 6 months
Title
Assess child's autonomy regarding his treatments
Description
Reporting in connected device
Time Frame
4 to 6 months
Title
Assess the intake treatments quality
Description
Questionnaire for parents on difficulties frequency with checked answers (no specific scale available)
Time Frame
4 to 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
3 Years
Maximum Age & Unit of Time
11 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Child volunteer from 3 to 11 years old Affected by cystic fibrosis With a prescription containing at least two medications twice a day Affiliation to the national health insurance Child and holder of the exercise of parental authority understands and speaks French The person exercising parental authority must have reached the age of majority. Collection of the written consent of one of the holders of the exercise of parental authority Exclusion Criteria: Non-voluntary child, under 3 years of age or over 12 years of age Family reluctant to technology Family without smartphone and/or wifi connection Failure to obtain the written consent of one of the holders of the exercise of parental authority Child involved in research involving the human person
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Marie JAMIN
Phone
+33296017818
Email
marie.jamin@ch-stbrieuc.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Gwenaëlle LE GARFF
Phone
+33296017277
Email
gwenaelle.legarff@armorsante.bzh
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marie JAMIN
Organizational Affiliation
Centre Hospitalier de Saint-Brieuc
Official's Role
Principal Investigator
Facility Information:
Facility Name
Chu Rennes
City
Rennes
ZIP/Postal Code
35000
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Eric DENEUVILLE
Facility Name
Centre Hospitalier de Saint-Brieuc
City
Saint-Brieuc
ZIP/Postal Code
22000
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marie JAMIN

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
14667488
Citation
De Geest S, Sabate E. Adherence to long-term therapies: evidence for action. Eur J Cardiovasc Nurs. 2003 Dec;2(4):323. doi: 10.1016/S1474-5151(03)00091-4. No abstract available.
Results Reference
result
PubMed Identifier
19416142
Citation
Jentzsch NS, Camargos PAM, Colosimo EA, Bousquet J. Monitoring adherence to beclomethasone in asthmatic children and adolescents through four different methods. Allergy. 2009 Oct;64(10):1458-1462. doi: 10.1111/j.1398-9995.2009.02037.x. Epub 2009 Mar 28.
Results Reference
result
PubMed Identifier
16387243
Citation
Zindani GN, Streetman DD, Streetman DS, Nasr SZ. Adherence to treatment in children and adolescent patients with cystic fibrosis. J Adolesc Health. 2006 Jan;38(1):13-7. doi: 10.1016/j.jadohealth.2004.09.013.
Results Reference
result
PubMed Identifier
8658364
Citation
Conway SP, Pond MN, Hamnett T, Watson A. Compliance with treatment in adult patients with cystic fibrosis. Thorax. 1996 Jan;51(1):29-33. doi: 10.1136/thx.51.1.29.
Results Reference
result
PubMed Identifier
18304896
Citation
Arias Llorente RP, Bousono Garcia C, Diaz Martin JJ. Treatment compliance in children and adults with cystic fibrosis. J Cyst Fibros. 2008 Sep;7(5):359-67. doi: 10.1016/j.jcf.2008.01.003. Epub 2008 Mar 4.
Results Reference
result
PubMed Identifier
27060726
Citation
Sanchis J, Gich I, Pedersen S; Aerosol Drug Management Improvement Team (ADMIT). Systematic Review of Errors in Inhaler Use: Has Patient Technique Improved Over Time? Chest. 2016 Aug;150(2):394-406. doi: 10.1016/j.chest.2016.03.041. Epub 2016 Apr 7.
Results Reference
result
PubMed Identifier
25233386
Citation
O'Donohoe R, Fullen BM. Adherence of subjects with cystic fibrosis to their home program: a systematic review. Respir Care. 2014 Nov;59(11):1731-46. doi: 10.4187/respcare.02990. Epub 2014 Jul 15.
Results Reference
result
PubMed Identifier
28056541
Citation
Britto MT, Rohan JM, Dodds CM, Byczkowski TL. A Randomized Trial of User-Controlled Text Messaging to Improve Asthma Outcomes: A Pilot Study. Clin Pediatr (Phila). 2017 Dec;56(14):1336-1344. doi: 10.1177/0009922816684857. Epub 2017 Jan 5.
Results Reference
result
Links:
URL
https://www.20minutes.fr/sante/2660383-20191129-maladies-comment-applications-objets-connectes-peuvent-aider-enfants-prendre-traitement
Description
Maladies : Comment les applications et objets connectés peuvent aider les enfants à prendre leur traitement ?

Learn more about this trial

Use of a Connected Companion in Children With Cystic Fibrosis

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