N/A
Completed N=29
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
| Outcome | Result | p-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.
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.