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Type 2 Diabetes Self-management Intervention for Low-income Women

A Comprehensive Approach to Type 2 Diabetes Self-management for Low-income Women

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01284465
Enrollment
56
Registered
2011-01-27
Start date
2011-01-31
Completion date
2014-12-31
Last updated
2015-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Type 2 Diabetes

Keywords

Type 2 diabetes self-management, Minority women, Barriers to diabetes self-management

Brief summary

The purpose of this study is to assess the extent to which a culturally appropriate, self-management intervention that combines patient education with a patient outreach liaison strategy improves outcomes associated with type-2 diabetes among low-income diabetic women.

Detailed description

In recent years, the prevalence of diabetes has significantly increased among women and because of the expected fast growth rate of minority populations, the number of women in these groups who will be diagnosed with diabetes is also expected to increase significantly over the coming years. Among women from minority groups diabetes is the fourth leading cause of death while it is the seventh among non-Hispanic White females. Non-compliance to diabetes self-care is a major concern for type 2 diabetic women of racial/ethnic groups because of the existing socio-economic and environmental barriers. Often, these women live in poverty; have less than a high school education as well as language barriers and inadequate health literacy, which further place them at risk for complications, and the daily activities of diabetes self-care are implemented within the context of family responsibilities and patient's priorities. This study is a 12-month randomized controlled trial designed to compare a lifestyle intervention group (combination group) and a control group (education only group). Participants assigned to either group will receive three group education sessions (baseline, 3 and 6 months) with an emphasis on self-management.

Interventions

BEHAVIORALEducation and patient liaison combination

Group education sessions with Patient liaison using ecological momentary assessment principles

BEHAVIORALControl group

Group education sessions at baseline, 3 and 6 months

Sponsors

National Center for Research Resources (NCRR)
CollaboratorNIH
Meharry Medical College
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
21 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. Low-income women ages 21 and older; With type 2 diabetes ( fasting plasma glucose \> 126 mg/dl); 2. At risk of developing diabetes related complications (treatments goals from The American Diabetes Association Standards of medical care) as defined by: * HbA1c \>8.0 % * Any of the metabolic clusters such as Pre-prandial plasma glucose \> 130 mg/dl; Obesity (BMI \>25 kg/m2, or waist circumference \>88 cm (\>35 in); Hypertension (Systolic \>130 and Diastolic \> 80 mmHg); Hyperlipidemia (Triglycerides \>150 mg/dL; HDL\<50 mg/dL; LDL \>100 mg/dL)

Exclusion criteria

* Participants will be excluded if they are currently pregnant, have conditions (i.e., end stage diagnosis) or behaviors likely to affect conduct of the trial, and unwilling to accept treatment assignment by randomization.

Design outcomes

Primary

MeasureTime frameDescription
HbA1cbaseline, 6 and 12 monthsglycosylated hemoglobin

Secondary

MeasureTime frameDescription
Risk factors for co-morbidity and daily self-management behaviorsbaseline, 3, 6, 9 and 12 months1. -Risk factors for co-morbidity: 2. -Daily self-management behaviors

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026