Societal Burden Associated With Type 1 Diabetes in Canada
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorPeriPharm
About this trial
The purpose of this observational study is to estimate the burden of T1D on caregivers of patient with T1D in terms of work productivity, healthcare resource utilization and quality of life.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Parental caregiver of a child recently diagnosed (<= 2 years) with T1D before study inclusion;
Age ≥18 ;
Residence in the Canada;
Willingess to complete a 20-minute survey
Disqualifiers
None
Trial population
Parental caregivers of a child with T1D
Trial design
Design model
Cohort
Time perspective
Cross-sectional
Treatments tested in this trial
observational study
Other interventionThis is an observational study in which participants complete PRO questionnaires via a web platform. No medical intervention or medication is involved.
Treatment groups
100 Participants
are divided into 1 treatment groupGroup A: Caregiver of child with T1D1 intervention
Trial outcomes
Primary outcomes
1
To estimate work productivity impairment of caregivers of a T1D child.
Using the WOrk Productivity and Activity Impairment (WPAI) questionnaire
Time frame
At recruitmentSecondary outcomes
1
To estimate healthcare resource utilization in caregivers of T1D child
Using the modified Resource Utilization Questionnaire for Type 1 Diabetes (mRUQ-T1DM) questionnaire.
Time frame
At recruitment2
To estimate health-related quality of life in caregivers of a T1D child
Using the EuroQOL-5 dimension-5 levels (EQ-5D-5L) questionnaire.
Time frame
At recruitment3
To estimate the caregiver burden in caregivers of a T1D child
Using the Zarit Burden Interview-22 (ZBI-22) questionnaire.
Time frame
At recruitmentSponsors and contacts
Click on the lead sponsor to view all of their trials.
PeriPharm
Lead sponsor
Sanofi
Collaborator
Source ClinicalTrials.gov