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N/A Completed N=29 Randomized Treatment

Impact of a Diabetes Transitions Tool Kit on Post-Hospitalization Glycemic Control

Source: ClinicalTrials.gov NCT01495975 ↗
Enrolled (actual)
29
Serious AEs
0.0%
Results posted
Apr 2015
Primary outcomePrimary: Glycemic Control — 144; 172 mg/dL

Summary

The goal of this research is to evaluate the impact and feasibility of using web-based patient-provider communication and a remote glucose monitoring tool to improve post-hospitalization glycemic control and patient self-care. The investigators hypothesize that providing patients this web-based tool over a 4-week period after discharge to home will result in more effective glycemic control compared to usual care, and that patients with access to the "tool kit" will have a trend towards improved diabetes self-management and less diabetes-related distress.

Outcome Measures

OutcomeResultp-value
PRIMARY
Glycemic Control
144; 172 —
SECONDARY
Diabetes Distress
— —
SECONDARY
Diabetes Self-Management
— —
SECONDARY
Unplanned Readmission or ED Visit
— —

Eligibility Criteria

Inclusion Criteria

  • Age 18 years or older
  • English speaking and able to read English
  • Diagnosis of type 2 diabetes (new and pre-existing)
  • Hospital admission with endocrinology or inpatient diabetes management consult
  • On insulin during hospitalization with plan for continuation upon discharge.
  • Discharge planned for home.
  • Access to the internet and an active email account throughout the 6-week study period.

Exclusion Criteria

  • Inability to connect to, navigate, and utilize the web-based system, or designate someone who is capable of using the system.
  • No identifiable outpatient healthcare provider.
  • Pregnancy, ruled out by urine hCG test after consent is obtained in all women who continue to have menstrual cycles.
  • End-stage liver disease with prothrombin time >15 seconds and albumin <3 mg/dL.
  • Hypoglycemia unawareness: patient lacks sensation of common signs of blood glucose <60 mg/dL (tachycardia, diaphoresis, hunger, confusion, fatigue).
  • Projected survival <1 year.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01495975). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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