Ignite Creation Date:
2024-05-06 @ 7:48 PM
Last Modification Date:
2024-10-26 @ 3:13 PM
Study NCT ID:
NCT06134934
Status:
RECRUITING
Last Update Posted:
2024-01-31
First Post:
2023-11-01
Brief Title:
TeleCare North Diabetes
Sponsor:
Aalborg University Hospital
Organization:
Aalborg University Hospital
Study Overview
Official Title:
TeleCare North Diabetes A Feasibility Study
Status:
RECRUITING
Status Verified Date:
2024-01
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This feasibility study will evaluate the feasibility of two telemonitoring designs for non-insulin treated T2D patients with an eye to identify the most suitable telemonitoring intervention for a future large-scale randomized trial
Detailed Description:
Background Maintaining optimal glycaemic control in type 2 diabetes T2D is difficult Telemedicine has potential to support poorly controlled people with T2D in the achievement of glycaemic control if the telemedicine solution includes a telemonitoring component However only few telemonitoring solutions for non-insulin treated T2D exist Therefore the aim of this feasibility study is to evaluate the feasibility of two telemonitoring intervention designs for non-insulin treated T2D patients with an eye to identify the most suitable telemonitoring intervention for a future large-scale randomized trial
Method The trial will be conducted as a three-month randomized feasibility study in four municipalities in North Denmark with 15 participants from each municipality Two different telemonitoring intervention designs will be tested One intervention will include self-monitoring of blood glucose SMBG together with monitoring of sleep and mental health The second intervention will include an identical setup but with the addition of blood pressure and activity monitoring Two municipalities will be allocated to one intervention design whereas the other two municipalities will be allocated to the second intervention design Qualitative interviews with participants and clinicians will be conducted to gain insight into their experiences with and acceptance of the intervention designs and trial procedures eg blood sampling and questionnaires In addition differences in direct intervention costs between the two alternative interventions will be evaluated
Method The trial will be conducted as a three-month randomized feasibility study in four municipalities in North Denmark with 15 participants from each municipality Two different telemonitoring intervention designs will be tested One intervention will include self-monitoring of blood glucose SMBG together with monitoring of sleep and mental health The second intervention will include an identical setup but with the addition of blood pressure and activity monitoring Two municipalities will be allocated to one intervention design whereas the other two municipalities will be allocated to the second intervention design Qualitative interviews with participants and clinicians will be conducted to gain insight into their experiences with and acceptance of the intervention designs and trial procedures eg blood sampling and questionnaires In addition differences in direct intervention costs between the two alternative interventions will be evaluated
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None