DIgital Assisted MONitoring for DiabeteS - I (DIAMONDS)
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ClinicalTrials.gov Identifier: NCT01804803 |
Recruitment Status :
Completed
First Posted : March 5, 2013
Last Update Posted : June 4, 2020
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Condition or disease | Intervention/treatment | Phase |
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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 |

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 |

Arm | Intervention/treatment |
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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.
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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.
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Procedure: Use of regular glucometer |
- Changes in HbA1c from baseline value [ Time Frame: 3-month, 6-month ]
- Changes in HbA1c from baseline value in relation to HbA1c value at baseline [ Time Frame: 6-month ]
- Percentages of patients with HbA1c >8.5% at 3 and 6 months [ Time Frame: 3-month, 6-month ]
- Percentages of patients with HbA1c <7.0% at 3 and 6 months [ Time Frame: 3-month, 6-month ]
- Percentages of patients with HbA1c <6.5% at 3 and 6 months [ Time Frame: 3-month, 6-month ]
- Differences in fasting blood glucose levels [ Time Frame: 3-month, 6-month ]
- 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 ]
- Frequency of hypoglycaemic episodes and relationship with changes in therapy [ Time Frame: 3-month, 6-month ]
- Changes in therapy (drug type and doses; in relation to SMBG values) [ Time Frame: 3-month, 6-month ]
- Appropriateness of glucose testing (% conformity based on recommended frequency of testing, also in relation to meals) [ Time Frame: 3-month, 6-month ]
- Indices of glucose variability (Kovatchev's LBGI, HBGI, ADRR) [ Time Frame: 3-month, 6-month ]
- Quality of life [ Time Frame: 6-month ]
- Proportion of subjects with eGFR less than 60 and high LBGI, HBGI, or ADRR indices [ Time Frame: 3-month, 6-month ]
- 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 ]

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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 |
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.

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
Italy | |
University of Bari Aldo Moro | |
Bari, BA, Italy, 70124 | |
IRCSS Casa Sollievo Sofferenza | |
San Giovanni Rotondo, FG, Italy | |
University of Foggia | |
Foggia, Italy |
Principal Investigator: | Francesco Giorgino, M.D., Ph.D. | University of Bari Aldo Moro |
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
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 |
glycated hemoglobin hyperglycemia hypoglycemia |
insulin self-monitoring of blood glucose telemedicine |