Evaluation of an Early Screener to Identify Long-term Problems With Regard to Metabolic Control and Treatment Adherence Among Children and Adolescents With Type 1 Diabetes

Sponsor
University Children's Hospital, Zurich (Other)
Overall Status
Completed
CT.gov ID
NCT03642483
Collaborator
(none)
61
1
43.4
1.4

Study Details

Study Description

Brief Summary

Background: Type 1 diabetes is one of the most common chronic illnesses among children and adolescents. Although, intensive medical care is provided for these patients, some of them have poor metabolic control. For example, only 21% of adolescents with type 1 diabetes in the USA achieve the recommended average blood sugar concentration (HbA1c<7.5%). This is a major problem, since chronic hyperglycemia is the primary cause of morbidity and mortality in type 1 diabetes and causes several serious complications, for example kidney failure, blindness, and stroke. Therefore, the International Society for Pediatric and Adolescent Diabetes (ISPAD) declared psychosocial factors, to be the most important risk factors of poor type 1 diabetes Management. Therefore, an instrument is needed to identify children and adolescents with poor metabolic control in their course of disease as soon as possible. With an early identification of such risk patients, better support can be provided. However, there is no such instrument yet for pediatric patients with type 1 diabetes. To fill this gap, a questionnaire (FEPB) based on the PAT 2.0© (Psychosocial Assessment Tool; an instrument used in oncology) was developed for this project.

Aim: The aim of this project is to evaluate and validate a new instrument (FEPB) for an early identification of children and adolescents with poor metabolic control in their course of disease in a longitudinal design.

Method: The sample consists of children and adolescents (age: 5-18 years), who were newly diagnosed with type 1 diabetes (2-4 weeks ago), and who are in care at the University Children's Hospital of Zurich. Structured interviews are conducted with the patients and the parents are asked to fill out some questionnaires at two times: first, 2-4 weeks after the diagnosis (T1) and second 6 month later (T2). With the new instrument (FEPB) a risk score can be calculated for each patient at T1. Statistical analysis will be performed to determine whether that risk score can predict which patients have poor metabolic control (HbA1c > 7.5%) at T2.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    61 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Evaluation of an Early Screener to Identify Long-term Problems With Regard to Metabolic Control and Treatment Adherence Among Children and Adolescents With Type 1 Diabetes
    Actual Study Start Date :
    Jun 5, 2018
    Actual Primary Completion Date :
    Jan 17, 2022
    Actual Study Completion Date :
    Jan 17, 2022

    Outcome Measures

    Primary Outcome Measures

    1. HbA1c [10 minutes]

      Glycated hemoglobin

    Secondary Outcome Measures

    1. health-related quality of life (Chronic generic measure) [5 minutes]

      Assessed by questionnaire: DISABKIDS Chronic generic measure - short version (DCGM-12; the European DISABKIDS Group, 2012). Total score range: 12-60. The higher the score, the higher the health-related quality of life.

    2. health-related quality of life (diabetes module) [5 minutes]

      Assessed by questionnaire: DISABKIDS diabetes module (The European DISABKIDS Group, 2012). Total score range: 10-50. The higher the score, the higher the health-related quality of life.

    3. psychological health (Depression) [10 minutes]

      Assessed by questionnaire: German Version of the Children's Depression Inventory (Depressionsinventar für Kinder und Jugendliche [DIKJ]; Stiensmeier-Pelster, Braune-Krickau, Schürmann & Duda, 2014). Total score range: 0-58. The higher the score, the more depressed the participants are.

    4. psychological health (Trait-Anxiety) [5 minutes]

      Assessed by questionnaire: German Version of the Trait-Anxiety Inventory for Children (Trait Angstinventar für Kinder [STAIK-T]; Unnewehr, Joormann, Schneider & Margraf, 1992). Total score range: 20-60. The higher the score, the higher the trait anxiety.

    5. psychological health (Child Behavior) [10 minutes]

      Assessed by questionnaire: German Version of the Child Behavior Checklist (CBCL 6-18R; Döpfner, Plück & Kinnen, 2014) Total score range: 0-224. The higher the score, the more behavioral problems.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    5 Years to 18 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • diagnosed with type 1 Diabetes 2-4 weeks ago

    • in care at the University Children's Hospital of Zurich

    • German speaking

    Exclusion Criteria:
    • other severe illness that affects the diabetes Management

    • severe developmental disorder

    • pregnancy

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University Children's Hospital Zurich Zürich Switzerland

    Sponsors and Collaborators

    • University Children's Hospital, Zurich

    Investigators

    • Principal Investigator: Markus A Landolt, Prof. dr., University Children's Hospital, Zurich
    • Principal Investigator: Daniel Konrad, Prof. dr., University Children's Hospital, Zurich

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    University Children's Hospital, Zurich
    ClinicalTrials.gov Identifier:
    NCT03642483
    Other Study ID Numbers:
    • 2018-00374-G1
    First Posted:
    Aug 22, 2018
    Last Update Posted:
    Apr 21, 2022
    Last Verified:
    Apr 1, 2022
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by University Children's Hospital, Zurich
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 21, 2022