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DIgital Assisted MONitoring for DiabeteS - I (DIAMONDS)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT01804803
Recruitment Status : Completed
First Posted : March 5, 2013
Last Update Posted : June 4, 2020
Sponsor:
Collaborators:
Eli Lilly and Company
LifeScan
Information provided by (Responsible Party):
Francesco Giorgino, M.D., Ph.D., University of Bari

Brief Summary:
The study aims to validate the clinical efficacy of a telemedicine- and web-based system platform for Self-monitoring of blood glucose (SMBG) data transmission and analysis in terms of improved metabolic control, assessed by measuring changes in HbA1c, in insulin-treated diabetic patients. The system platform involves (i.) systematic (real-time and anywhere) transmission of SMBG data to a decision supported software (DSS)-assisted server, (ii.) web-based analysis of data, and (iii.) feedback on patients and medical staff to implement metabolic control. The expected outcome is that using this telemedicine-based system with transmission of SMBG data, web-based analysis of data and medical feedback to patients and medical team will improve glucose control in insulin-treated individuals with type 1 or type 2 diabetes mellitus.

Condition or disease Intervention/treatment Phase
Diabetes Mellitus Procedure: Use of software-implemented glucometer for real-time collection and transmission of measured glucose values to remote server. Procedure: Use of regular glucometer Not Applicable

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 123 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A Telemedicine-based Intervention Study Involving Real-time and Anywhere Transmission of Blood Glucose Data to a Decision Supported Software-assisted Server With Web-based Analysis of Data and Medical Feedback on Metabolic Control.
Actual Study Start Date : September 9, 2013
Actual Primary Completion Date : November 30, 2017
Actual Study Completion Date : November 30, 2017

Resource links provided by the National Library of Medicine

Drug Information available for: Dextrose

Arm Intervention/treatment
Experimental: T-SMBG
This group will perform SMBG using a smartphone-connected glucometer implemented with a software for real-time collection and transmission of measured glucose values to the remote server. SMBG results will be immediately transmitted to the remote server, which will perform data collection and analysis, and provide feed-back to the patient and the medical staff according to pre-defined specific algorithms (Decision Supported Software, DSS). A specific algorithm incorporated into the DSS will allow the patients to self-calculate the dose of basal insulin to be administered according to the measured fasting blood glucose levels for consecutive periods of three days. Glucose data and analyses will be made accessible to the patients and medical staff anytime and anywhere via the web. Patients will be also assisted by the diabetes medical team located at or connected with a call center 24-hours/day, 7 days/week.
Procedure: Use of software-implemented glucometer for real-time collection and transmission of measured glucose values to remote server.
Device is a smartphone-connected glucometer. The smartphone will be implemented with a software for real-time collection and transmission of measured glucose values to the remote server. Thus, the glucometer will be made "hot" for real-time and anywhere data transmission. In addition, at the time of blood glucose measuring, the patient will enter information on whether the measurement is being performed in the pre-prandial, post-prandial or absorptive periods, and will indicate which meals the measurement refers to (i.e., breakfast, lunch, dinner, snack). SMBG results will be immediately transmitted to the remote server, which will perform data collection and analysis, and provide feed-back to the patient and the medical staff according to pre-defined specific algorithms (Decision Supported Software, DSS).

Active Comparator: SMBG
This group will perform SMBG using a regular glucometer and will report glucose data on paper charts (or download data from the glucometer onto the PC) at the planned study visits. Patients will not receive feed-back on their glucose levels nor instructions on how to potentially modify their drug therapy except when undergoing medical visits at the planned intervals. Patients, finally, will not be assisted by the diabetes team/call center.
Procedure: Use of regular glucometer



Primary Outcome Measures :
  1. Changes in HbA1c from baseline value [ Time Frame: 3-month, 6-month ]

Secondary Outcome Measures :
  1. Changes in HbA1c from baseline value in relation to HbA1c value at baseline [ Time Frame: 6-month ]
  2. Percentages of patients with HbA1c >8.5% at 3 and 6 months [ Time Frame: 3-month, 6-month ]
  3. Percentages of patients with HbA1c <7.0% at 3 and 6 months [ Time Frame: 3-month, 6-month ]
  4. Percentages of patients with HbA1c <6.5% at 3 and 6 months [ Time Frame: 3-month, 6-month ]
  5. Differences in fasting blood glucose levels [ Time Frame: 3-month, 6-month ]
  6. Differences in blood glucose levels in the pre-prandial and post-prandial phases; meal-related glucose excursions (post/pre-meal "delta") [ Time Frame: 3-month, 6-month ]
  7. Frequency of hypoglycaemic episodes and relationship with changes in therapy [ Time Frame: 3-month, 6-month ]
  8. Changes in therapy (drug type and doses; in relation to SMBG values) [ Time Frame: 3-month, 6-month ]
  9. Appropriateness of glucose testing (% conformity based on recommended frequency of testing, also in relation to meals) [ Time Frame: 3-month, 6-month ]
  10. Indices of glucose variability (Kovatchev's LBGI, HBGI, ADRR) [ Time Frame: 3-month, 6-month ]
  11. Quality of life [ Time Frame: 6-month ]
  12. Proportion of subjects with eGFR less than 60 and high LBGI, HBGI, or ADRR indices [ Time Frame: 3-month, 6-month ]
  13. Subgroup analyses of changes in HbA1c from baseline according to patients' age (<45 yrs, >45yrs), type of diabetes (type 1, type 2), and diabetes duration (<5 yrs, >5 yrs) [ Time Frame: 6-month ]


Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 70 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • males and females
  • age 18-70 yrs;
  • insulin-treated diabetes (both type 1 and type 2 diabetes treated with at least 3 injections/day);
  • diabetes diagnosis from at least 1 year;
  • inadequate glycemic control (HbA1c ranging from 7.0% to 10.0%; local measurements within the last 6 weeks);
  • ability and willingness to carry out SMBG;
  • informed consent.

Exclusion Criteria:

  • diagnosis of diabetes within less than 1 year;
  • impending complications of diabetes: proliferative retinopathy or maculopathy (with significant loss of visual function), severe renal failure (eGFR <30), severe neuropathy (autonomic dysfunction, peripheral neuropathy, gastroparesis);
  • clinically significant, active (over the past 12 months) disease of the cardiovascular, gastrointestinal, neurological, genito-urinary, haematological systems or severe uncontrolled hypertension (SBP >180 mmHg; DBP >100 mmHg);
  • diagnosis of active neoplasia within the last 5 years (history of chemotherapy or radiation treated malignancy within 5 years prior to study procedure, except for lymphoma);
  • pregnancy or intention to become pregnant during the study;
  • poor compliance to study procedures.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01804803


Locations
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Italy
University of Bari Aldo Moro
Bari, BA, Italy, 70124
IRCSS Casa Sollievo Sofferenza
San Giovanni Rotondo, FG, Italy
University of Foggia
Foggia, Italy
Sponsors and Collaborators
University of Bari
Eli Lilly and Company
LifeScan
Investigators
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Principal Investigator: Francesco Giorgino, M.D., Ph.D. University of Bari Aldo Moro
Publications:
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
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Responsible Party: Francesco Giorgino, M.D., Ph.D., Professor of Endocrinology, University of Bari
ClinicalTrials.gov Identifier: NCT01804803    
Other Study ID Numbers: DIAMONDS-I
First Posted: March 5, 2013    Key Record Dates
Last Update Posted: June 4, 2020
Last Verified: June 2020
Keywords provided by Francesco Giorgino, M.D., Ph.D., University of Bari:
glycated hemoglobin
hyperglycemia
hypoglycemia
insulin
self-monitoring of blood glucose
telemedicine