Community-Based Diabetes Care for Korean American Immigrants

Status Completed

Clinical Trial Summary

The primary aims are to test the effectiveness of the self-help DM intervention (SHIP-DM), a comprehensive, culturally tailored DM management intervention, in improving glucose outcomes; To determine the effectiveness of the SHIP-DM in KAI with type 2 DM in improving self-care skills and psycho-behavioral outcomes related to DM control, to develop tangible infrastructures for the dissemination of valid and effective education materials to a wider population of KAI with type 2 DM in the US (e.g., audio-visual education materials, web-based intervention materials, mobile telephone-based intervention materials) and to explore the feasibility and acceptability of each dissemination module, utilizing the delayed intervention group participants. The secondary aims are to obtain preliminary cost-effectiveness data related to the proposed intervention, including cost estimates for this type of DM intervention, and to establish a systematic, long-term dissemination plan, including documenting effective methodologies, to facilitate faster translation of research findings and products to direct consumers in non-research settings.

Clinical Trial Description

Inclusion Criteria

1. Self-identified as a first generation Korean American

2. Type 2 diabetes

3. Age 30-75 years

4. Resides in Washington-Baltimore area

5. Self-identified with DM and HbA1c >= 7.0 % within 6 months of screening

6. Expresses willingness to participate in all aspects of the study over its full course

Exclusion criteria

1. Unable to give informed consent

2. Physical or mental health conditions that could limit active participation in the study (e.g., blindness in both eyes, severe immobility, psychiatric diseases)

3. Hematological condition that would affect A1C assay, e.g., hemolytic anemia, sickle cell anemia

4. Past experience in diabetes group education ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01264796
Study type	Interventional
Source	University of Texas at Austin
Contact
Status	Completed
Phase	N/A
Start date	November 2009
Completion date	August 2015

View Details

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