A Pilot Study of Diabetes Risk Reduction Program With WIC Mothers(The Special Supplemental Nutrition Program for Women, Infants, and Children) Overweight WIC Mothers
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Purpose
1) to evaluate treatment fidelity of DRRP: study design, training of interventionists, delivery and receipt of the intervention, and application of the intervention in real-life settings; 2) to identify successful strategies for participant recruitment and maintaining active participation; 3) to collect and analyze preliminary indicators of DRRP's effect on dietary intake, physical activity, stress responses, and body weight; and 4) To evaluate sample representativeness of the target audience, implementation and acceptability of DRRP, and attrition rate.
| Condition | Intervention | Phase |
|---|---|---|
|
Prevention of Weight Gain |
Other: lifestyle intervention |
Phase 3 |
| Study Type: | Interventional |
| Study Design: | Primary Purpose: Prevention |
| Official Title: | A Pilot Study of Diabetes Risk Reduction Program With Overweight WIC Mothers |
- body weight
- dietary fat intake, fruit and vegetable intake, physical activity, stress, affects
| Arms | Assigned Interventions |
|---|---|
|
Experimental: lifestyle intervention
Control group: usual WIC care
|
Other: lifestyle intervention |
Eligibility| Ages Eligible for Study: | 18 Years to 34 Years |
| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:Non-pregnant women between 18 and 34 years old who understood and spoke English and had a measured BMI between 25.0 and 39.9 kg/m2 were eligible for this study. Additional inclusion criteria included having a youngest child between 6 weeks and 3.5 years of age enrolled in one of our three collaborating WIC locations, not planning to become pregnant or change WIC clinics during the study, providing accurate contact information, agreeing to notify researchers with changes in contact information or pregnancy status, willingness to accept randomized participation assignments, being willing to participate in the project for 1.5 years, and consenting to have blood glucose tested via finger stick.
Exclusion Criteria: women with fasting blood glucose greater than 126 mg/dl or random blood glucose greater than 200 mg/dl, self-reported type 1 or 2 diabetes or an eating disorder, or inability to walk more than one block without resting or shortness of breath were excluded. Eligible participants provided their individual telephone and address and a telephone number of one back-up contact (relative, friend, or neighbor).
Contacts and Locations| United States, Michigan | |
| Michigan Stat University College of Nursing | |
| East Lansing, Michigan, United States, 48824 | |
| Michigan State University College of Nursing | |
| East Lansing, Michigan, United States, 48824 | |
More Information
No publications provided by National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| ClinicalTrials.gov Identifier: | NCT00944060 History of Changes |
| Other Study ID Numbers: | DK74511 (completed), 1R34DK074511-01A1 |
| Study First Received: | July 20, 2009 |
| Last Updated: | January 14, 2010 |
| Health Authority: | United States: NIDDK United States: Federal Government |
Additional relevant MeSH terms:
|
Weight Gain Overweight Body Weight Changes Body Weight Signs and Symptoms |
ClinicalTrials.gov processed this record on May 21, 2013