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Clinical Trials/ISRCTN71674628
ISRCTN71674628
Completed
Not Applicable

The impact of a telemetric monitoring service in type 2 diabetes: a randomised controlled trial

niversity of Edinburgh (UK)0 sites320 target enrollmentMay 6, 2011

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Topic: Diabetes Research Network, Primary Care Research Network for England, Scottish Primary Care Research Network and Scottish Diabetes Research network
Sponsor
niversity of Edinburgh (UK)
Enrollment
320
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
May 6, 2011
End Date
TBD
Last Updated
9 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
niversity of Edinburgh (UK)

Eligibility Criteria

Inclusion Criteria

  • Patients registered with general practices in the selected areas who:
  • 1\. Are on their practice diabetes registers
  • 2\. Have type 2 diabetes which is managed mainly in general practice
  • 3\. Are aged bewteen 18 and 79 years
  • 4\. Have a last recorded haemoglobin A1c (HbA1c) measurement \> 7\.5% (\>59 mmol/mol)
  • 5\. Have a last recorded blood pressure \> 135/80mmHg and average daytime self monitored systolic blood pressure \>1 30/75 mmHg
  • 6\. Have given informed consent
  • 7\. Have a mobile telephone signal available from home.; Target Gender: Male \& Female; Upper Age Limit 79 years ; Lower Age Limit 18 years

Exclusion Criteria

  • Patients who:
  • 1\. Are aged 80 and above
  • 2\. Have an average systolic blood pressure \=120/70 or \> 210/135 mmHg taken by the research nurse at the consent visit
  • 3\. Have HbA1c \< 7\.5% (\< 59 mmol/mol)
  • 4\. Have hypertension or renal disease being managed in secondary care
  • 5\. Have had treatment for a cardiac event, or other life\-threatening illness within the past 6 months or have had surgery within the last 3 months
  • 6\. Are unable to consent
  • 7\. Are unable to use self\-monitoring equipment;
  • 8\. Have atrial fibrillation
  • 9\. Are pregnant

Outcomes

Primary Outcomes

Not specified

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