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Self-monitoring of Blood Glucose in Insulin-treated Patients With Type 2 Diabetes

Self-monitoring of Blood Glucose in Insulin-treated Patients With Type 2 Diabetes: a 9-month Randomised Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01460459
Enrollment
150
Registered
2011-10-26
Start date
2011-05-31
Completion date
2012-07-31
Last updated
2011-10-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetes Mellitus, Type 2

Keywords

diabetes, self-monitoring of blood glucose, frequency

Brief summary

Primary Objective: The objective of the study is to investigate the effect of a specific frequency of Self-monitoring of blood glucose (SMBG) on glycemic control and quality of life in patients with type 2 diabetes and who are in stable good glycemic control and using 1 insulin injection daily. The research question is: Does a less intensive frequency of SMBG in insulin-treated patients with type 2 diabetes, who are in stable good glycemic control, using 1 insulin injection daily, lead to a clinically relevant increase of HbA1c (an increase of 0.5%) and what is the effect on quality of life? Secondary objectives: The secondary objectives is to investigate the effect of a specific frequency of SMBG on the number of hypo and hyper glycaemia, number of extra diabetes-related contacts with the health care provider, and the diabetes medication.

Detailed description

SUMMARY Rationale: Self-monitoring of blood glucose (SMBG) is an important tool in diabetes care to achieve and maintain good glycemic control. But how often 'should' the patient measure the capillary glucose concentration? There is no general agreement between professionals, and there is no evidence for a specific frequency and timing. Objective: The objective of the study is to investigate the effect of a specific frequency of SMBG on glycemic control and quality of life in patients with type 2 diabetes and who are in stable good glycemic control and using 1 insulin injection daily. Study design: An open Randomised Controlled Trial. Study population: Patients with insulin-treated diabetes type 2, \> 18 years of age, using 1 insulin injection daily, performing SMBG \> 1 year, HbA1c ≤ 58 mmol/mol (\< 7.5%) in the preceding 12 months, sufficient knowledge of the Dutch language, no hypo-unawareness, no serious co-morbidity Intervention: Patients are instructed to measure their blood glucose concentrations 4 times per day (pre-prandial and before bedtime) one day weekly in group A, one day per two weeks in group B and one day monthly in group C. Patients are asked to keep a diary with the readings and the probably extra measurements, including the reasons. Main study parameters/endpoints: The main study parameters are glycemic control and quality of life. A difference of \> 0.5% (\> 5.5 mmol/mol) in HbA1c is considered to be relevant. Quality of life is measured with 3 validated questionnaires. Nature and extent of the burden and risks associated with participation, benefit and group relatedness: Patients in this study are used to perform SMBG. During the study, they are asked to monitor their glucose concentrations in a controlled, specific frequency (different kind of usual care are compared). And they are asked to fill in 3 questionnaires in the beginning and at the end of the study. Extra HbA1c measurements can be necessary. No side effects are expected, but safety is incorporated through HbA1c measurements every 3 months and every 3 months the diary will be discussed in the scheduled visits. Furthermore, extra measurements are allowed when necessary.

Interventions

BEHAVIORALa specific frequency of SMBG

Patients are instructed to measure their blood glucose concentrations 4 times per day (pre-prandial and before bedtime: high frequency: one day weekly middle frequency:one day per two weeks low frequency:one day monthly

Sponsors

Sanofi
CollaboratorINDUSTRY
Medical Research Foundation, The Netherlands
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients with insulin-treated diabetes type 2 * \> 18 years of age * using 1 insulin injection daily, * performing SMBG \> 1 year * HbA1c ≤ 58 mmol/mol (\< 7.5%) in the preceding 12 months * sufficient knowledge of the Dutch language.-

Exclusion criteria

* no hypo-unawareness * no serious co-morbidity (as judged by their own GP) * patients who measure their blood glucose concentration (4 measurements a day) more than once a week on average

Design outcomes

Primary

MeasureTime frameDescription
HbA1c9 monthsThe main study parameter is glycemic control. Glycemic control is measured by HbA1c. A difference of 0.5% (\> 5.5 mmol/mol) in HbA1c between groups is considered to be relevant.

Secondary

MeasureTime frameDescription
quality of life9 monthsThe secondary study parameter is quality of life. The quality of life is measured by 3 validated questionnaires: the 12-item Short Form Health Survey, the 20-item Problems Areas in Diabetes Scale (PAID) and the 13-item Summary of Diabetes Self care Activities. Furthermore, the glucose concentrations measured by SMBG should be between 4-7 mmol/l, preprandial and between 8-10 mmol/l before bed time. The endpoint is the number of glucose concentrations who are out of range at every 4th week.The number of hypo and hyperglycaemia are reported in the diary.

Countries

Netherlands

Contacts

Primary ContactJohanna Hortensius, RN
h.hortensius@isala.nl0031-38-4247763
Backup ContactNanne Kleefstra, MD PhD
n.kleefstra@isala.nl0031-38-4244013

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 24, 2026