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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01288300
Other study ID # 10-526-A
Secondary ID 1K23DK087903-01A
Status Completed
Phase N/A
First received January 27, 2011
Last updated September 23, 2013
Start date March 2011
Est. completion date April 2013

Study information

Verified date September 2013
Source University of Chicago
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

Main objective: To improve diabetes outcomes among Mexican-Americans with diabetes through church-based, culturally tailored, diabetes self-management interventions linked to the local healthcare system.

Specific Aim: To pilot test a church-based, culturally tailored diabetes self-management intervention to improve diabetes outcomes among low-income Mexican-American with diabetes

H1 A church-based diabetes self-care management curriculum partnered with the local healthcare system will improve glycosylated hemoglobin.

H2 A church-based diabetes self-care management curriculum partnered with the local healthcare system will improve systolic blood pressure and low-density lipids.

H3 A church-based diabetes self-care management curriculum partnered with the local healthcare system will improve diabetes related self-efficacy, self-empowerment and self-care management.


Description:

Diabetes is a very prevalent and morbid condition affecting Latinos, especially Mexican-Americans in the United States. South Lawndale, a predominately-Mexican neighborhood of Chicago, has a disproportionately high diabetes related mortality rate in comparison to the rest of Chicago and the U.S. Many church-based interventions have shown promise improving health outcomes among minority populations; but data on church-based interventions for Latino populations is scarce. Mobilizing community resources to develop church-based, diabetes self-management interventions may lead to sustainable, culturally tailored interventions, and improve outcomes in Latinos with diabetes. Considering the growth of the Hispanic population and their disproportionate burden of chronic diseases, developing programming aimed at decreasing the health disparities in this population is crucial. Our study proposes to fill this gap.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date April 2013
Est. primary completion date April 2013
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- over the age of 18

- able to speak either English or Spanish

- self-report of diagnosis of diabetes by a doctor

Exclusion Criteria:

- cannot give informed consent (e.g. due to intoxication or dementia)

- do not speak English or Spanish

- younger than 18 years old.

- pregnant women

- undergoing hemodialysis or treatment for cancer

- unable to attend 3- and 6-month follow up appointments

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
Picture good health/Imaginate una buena salud
Diabetes education, self-empowerment training, exercise, patient navigator
Diabetes lecture
Diabetes self-management lecture

Locations

Country Name City State
United States Centro de Salud y Esperanza Chicago Illinois
United States Our Lady of Tepeyac Church Chicago Illinois
United States St. Agnes of Bohemia Church Chicago Illinois

Sponsors (2)

Lead Sponsor Collaborator
University of Chicago National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Changes in glycosylated hemoglobin (Hba1c)from baseline at 3 and 6 months We will evaluate changes in HbA1c at baseline, at 3 months and then 6 months. We will analyze change in HbA1c from baseline and compare it to the 3 month and 6 month measures. baseline to 6 months No
Secondary Changes in systolic blood pressure at baseline, 3 and 6 months We will evaluate changes at baseline, at 3 months and then 6 months. We will analyze change from baseline and compare it to the 3 month and 6 month measures. baseline to 6 months No
Secondary Changes in low density lipoprotein from baseline to 3 and 6 month follow up We will evaluate changes from baseline, at 3 months and then 6 months. We will analyze change from baseline and compare it to the 3 month and 6 month measures baseline to 6 months No
Secondary Changes in diabetes self-care from baseline to 3 and 6 months We will evaluate changes from baseline, at 3 months and then 6 months. We will analyze change from baseline and compare it to the 3 month and 6 month measures baseline to 6 months No
Secondary Changes in diabetes self-empowerment from baseline to 3 and 6 months We will evaluate changes from baseline, at 3 months and then 6 months. We will analyze change from baseline and compare it to the 3 month and 6 month measures baseline to 6 months No
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