Clinical Trial to Assess Influence of MyCyFAPP Use on GI Related QOL in Children With Cystic Fibrosis

Cystic Fibrosis in Children Clinical Trial

— MyCyFAPP  

Official title:

Innovative Approach for Self-management and Social Welfare of Cystic Fibrosis Patients in Europe: Development, Validation and Implementation of a Telematics Tool. WP6.2: Impact Assessment Through a European Multicentre Clinical Trial: Validation of MyCyFAPP as a Portable System for Self-management in Children With CF

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT03292718
• Other study ID #: s60787
• Status: Not yet recruiting
• Phase: N/A
• First received: September 20, 2017
• Last updated: September 20, 2017
• Start date: October 2017
• Est. completion date: December 2018

Study information

• Verified date: September 2017
• Source: Universitaire Ziekenhuizen Leuven
• Contact: Mieke Boon, MD PhD
• Phone: +3216343820
• Email: mieke.boon[@]uzleuven.be
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Interventional trial to study the influence of the use of MyCyFAPP (mobile application) on the gastro-intestinal related quality of life.

This mobile APP has been developed during previous workpackages of the Horizon2020 Project and contains several modules:

• mathematical prediction model to calculate the needed dose for pancreatic enzyme replacement therapy

• educational games and other educational material

• communication with doctor/dietician through professional webtool

• diary to register symptoms and data on nutrition.

The app will be introduced and used during 6 months. Primary outcome parameter will be change in modified PedsQL GI after 3 months. PedsQL GI is an existing questionnaire that evaluates gastro-intestinal related quality of life in children. We validated it for use in cystic fibrosis in a previous observational study.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 200
• Est. completion date: December 2018
• Est. primary completion date: December 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 2 Years to 18 Years

Eligibility

Inclusion Criteria:

1. Diagnosis of CF as evidenced by one or more clinical feature consistent with the CF phenotype or positive CF newborn screen AND one or more of the following criteria:

1. A documented sweat chloride = 60 mEq/L by quantitative pilocarpine iontophoresis (QPIT)

2. A documented genotype with two disease-causing mutations in the CFTR gene

2. Having pancreatic insufficiency (stool elastase < 200 mcg/g stool) and using PERT

3. Age = 24 months and < 18 years at screening visit

4. Informed consent by parent or legal guardian; assent for children from age 12 years on

6. Inclusion visit coincides with scheduled routine clinic visit 7. Ability and willingness to comply with APP use and evaluations at time of routine clinic visits as judged by the site investigator 8. Availability of wifi connection at home so that connection to the internet is feasible at home at least weekly.

Exclusion Criteria:

1. Acute infection associated with decreased appetite or fever at time of run-in visit

2. Acute abdominal pain necessitating an intervention at time of run-in visit

3. Physical findings that would compromise the safety of the participant or the quality of the study data as determined by site investigator

4. Investigational drug use within 30 days prior to run-in visit

5. Started with CFTR modulator treatment less than 3 months before start of run-in visit

6. Inability to use the APP due to patient specific factors such as language or learning difficulties

Related Conditions & MeSH terms

• Cystic Fibrosis
• Cystic Fibrosis in Children
• Fibrosis

Intervention

Device:
• MyCyFAPP
use of the MycyFAPP with all its features during 6 months

Locations

Country	Name	City	State
n/a

Sponsors (3)

Lead Sponsor	Collaborator
Universitaire Ziekenhuizen Leuven	European Commission, Hospital Universitario La Fe

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	change in Modified PedsQL GI	Modified PedsQL GI will be assessed at month 0 and month 3 by applying questionnaires to children and their parents	3 months
Secondary	change in CFQ-R	CFQ-R will be assessed by questionnaires	3 months and 6 months
Secondary	change in VAS	VAS will be assessed by questionnaires	3 months and 6 months
Secondary	change in Modified PedsQL GI	Modified PedsQL GI will be assessed at month 0 and month 6 by applying questionnaires to children and their parents	6 months
Secondary	change in lung function	spirometry will be performed	3 and 6 months

External Links

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