Department of Endocrinology
Aalborg, 9000, Denmark
NCT Number: NCT04981808
The trial is an open-label randomized controlled trial. Patients with T2D on insulin therapy will be randomized to a telemonitoring group (intervention) and a usual care group (control). The telemonitoring group will use various devices at home. Hospital staff will monitor their data for a period of three months.
Looking for future studies?
Notify Me18 year and older
All sexes
Interventional
Not applicable
Aalborg, 9000, Denmark
The DiaMonT trial is an open-label randomized controlled trial with a trial period of three months conducted. The trial will be conducted in two sites in Denmark: Steno Diabetes Center North Jutland and Steno Diabetes Center Zealand. Patients with T2D on insulin therapy will be randomized (1:1) to a telemonitoring group (intervention) or a usual care group (control). The telemonitoring group will use an insulin pen, an activity tracker, a CGM, and a smartphone application throughout the trial period. Hospital staff (lab technicians and nurses) will monitor the telemonitoring groups' data and contact the subjects by telephone repeatedly throughout the trial period. The usual care group will use a blinded CGM the first and last 20 days of the trial and will use a blinded insulin pen for the entire period. The usual care groups' data will not be monitored during the trial.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Telemonitoring of CGM and insulin pen data
Time frame: At baseline to three months after randomization
Change in CGM time in range (3,9-10,0 mmol/L)
Time frame: At baseline to three months after randomization
Change in HbA1c
Time frame: At baseline to three months after randomization
Change in total daily dose of insulin (units)
Time frame: At baseline to three months after randomization
Change in time below range (CGM)
Time frame: At baseline to three months after randomization
Change in time above range (CGM)
Time frame: During the intervention
Number of days that the subjects wear the CGM
Time frame: During the intervention
Percentage of time that the CGM is active
Time frame: At baseline to three months after randomization
Mean glucose levels (mmol/l) measured by CGM
Time frame: At baseline to three months after randomization
Glycemic variability - percentage of cofficient of variation
Time frame: At baseline to three months after randomization
Time in hyperglycemia (>13,9 mmol/L)
Time frame: At baseline to three months after randomization
Time in hypoglycemia (<3,0 mmol/L)
Time frame: At baseline to three months after randomization
Number of episodes of hyperglycemia (>13,9 mmol/L)
Time frame: At baseline to three months after randomization
Number of episodes in hypoglycemia
Time frame: Through study completion, an average of 3 months
The frequency of use of the telemonitoring equipment
Time frame: Immediately after the intervention
Telemonitoring satisfaction and usability measured by the Telemonitoring Usability Questionnaire (TUQ). Minimum value =1, maximum value =7. A higher score = a better outcome
Time frame: From baseline to three months after randomization
Diabetes-related quality of life measured by the DIDP Questionnaire. Ranges from "very negative" to "very positive"
Time frame: From baseline to three months after randomization
Health-related quality of life measured by the Short Form 12 (SF-12). Options are not numeric
Aalborg University Hospital
Other
The Diabetes teleMonitoring of Patients in Insulin Therapy (DiaMonT) Trial: Study Protocol for a Randomized Controlled Trial
Acronym: DiaMonT
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT03437525
Diabetes Mellitus, Endocrine System Diseases
Shanghai, Shanghai Municipality, China
View Trial DetailsNCT05795439
Diabetes Mellitus, Endocrine System Diseases
Washington D.C., District of Columbia, United States
View Trial DetailsNCT06185296
Diabetes Mellitus, Endocrine System Diseases
Aalborg, North Jutland, Denmark
View Trial DetailsNCT03070106
Diabetes, Diabetes Mellitus
Cleveland, Ohio, United States
View Trial Details