Evaluation of the Omnipod DASH in Children and Adolescents With Type 1 Diabetes Mellitus

Sponsor
Jessa Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT05377385
Collaborator
(none)
40
1
5.6
7.1

Study Details

Study Description

Brief Summary

In this study the usability of the Omnipod DASH insulin administration system is evaluated prospectively by two questionnaires. The effect on the metabolic control is evaluated retrospectively by analysis of data from the medical records of the patients.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Questionnaire

Detailed Description

In the study the usability of the Omnipod DASH (= insulin patch pump) is evaluated prospectively by two questionnaires. The first questionnaire concerns practical items on the application of the pump (e.g. Is it easy to fill to pod?), the wearing of the pump (e.g. Is it comfortable to wear the pump?) and the comparison with insulin administration with insulin pens or other insulin pumps (e.g. is it less painful to administrate insulin by the Omnipod DASH pump). The second questionnaire asks for possible problems that the patients experienced during the wearing of the pump (e.g. did you experience an allergic skin reaction). The questions are formulated to be answered by a 5-point likert scale.

The metabolic control is studied retrospectively from data extracted from the medical records, i.e. the results of the determination of HbA1c and the results from continuous glucose monitoring (CGM) at the start, and after 2, 4 and 6 months of the wearing of the Omnipod DASH insulin pump.

Study Design

Study Type:
Observational [Patient Registry]
Anticipated Enrollment :
40 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Evaluation of the Usability and Effect on the Metabolic Control of the Omnipod DASH Insulin Administration System in Children and Adolescents With Type 1 Diabetes Mellitus
Actual Study Start Date :
Apr 13, 2022
Anticipated Primary Completion Date :
Sep 1, 2022
Anticipated Study Completion Date :
Oct 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Study group

Children and adolescents with type 1 diabetes mellitus who started in 2021 in the Jessa Hospital with the Omnipod DASH insulin administration device.

Behavioral: Questionnaire
Questionnaire about usability of the Omnipod DASH insulin administration system

Outcome Measures

Primary Outcome Measures

  1. Usability of and problems encountered with the Omnipod Dash insulin administration system [Through study completion, an average of 6 months]

    Usability of and problems encountered with the Omnipod Dash insulin administration system is evaluated by 2 home made questionnaire evaluated by a 5 point Likert scale. The first questionnaire includes 3 questions about the application of the pod (e.g. it is easy to place the pod), 7 questions about the wearing of the pod (e.g. the pod doesn't hinder me during sleeping) and 11 questions comparing insulin administration with insulin pens (e.g. insulin administration with the pod is more discrete). The second questionnaire includes 9 questions about possible problems with the Omnipod DASH insulin administration system (e.g. I developped an allergic skin reaction).

Secondary Outcome Measures

  1. Metabolic control of type 1 diabetes mellitus [Before and during the first 6 months of wearing the Omnipod Dash insulin administration system]

    Metabolic control of the type 1 diabetes mellitus measured by HbA1c levels and results from continuous glucose measurement data (e.g. time in range, time below range, time above range).

Eligibility Criteria

Criteria

Ages Eligible for Study:
6 Years to 18 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Children and adolescents with type 1 diabetes mellitus

  • Patients who started in 2021 with the Omnipod DASH insulin administration system in the Jessa Hospital

Exclusion Criteria:
  • Children and adolescents without type 1 diabetes mellitus

  • Children and adolescents with type 1 diabetes treated with insulin pens or other insulin pumps

Contacts and Locations

Locations

Site City State Country Postal Code
1 Jessa Hospital Hasselt Limburg Belgium B3500

Sponsors and Collaborators

  • Jessa Hospital

Investigators

  • Principal Investigator: Guy Massa, Jessa Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Jessa Hospital
ClinicalTrials.gov Identifier:
NCT05377385
Other Study ID Numbers:
  • 2022/018
First Posted:
May 17, 2022
Last Update Posted:
May 17, 2022
Last Verified:
May 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Jessa Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 17, 2022