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Community-Based Nutrition-Lifestyle Therapy for Pregnant Latina Women With Diabetes

Community-Based Nutrition-Lifestyle Therapy for Pregnant Latina Women With Diabetes

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06218147
Enrollment
15
Registered
2024-01-23
Start date
2024-04-01
Completion date
2025-03-27
Last updated
2025-04-03

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

Conditions

Diabetes Mel Gestational - in Pregnancy, Diabetes Mellitus, Type 2

Brief summary

Socioeconomically disadvantaged (SED) pregnant Latina women are disproportionately burdened by type 2 diabetes (T2D). Although lifestyle interventions can help to improve diabetes control, there are barriers to SED, Spanish-speaking pregnant people participating. The purpose of this proposal is to develop and test a culturally tailored, dietary-lifestyle behavioral intervention that supports eating plant-based foods such as fruits, vegetables, nuts and grains instead of processed foods and meat, and is implemented through community health workers (CHWs) to prevent excessive weight gain during pregnancy and improve control of blood sugar levels in pregnant Latina women with T2D. This study takes advantage of our existing strong relationships with the local Latino community, CHWs, and Santa Barbara County Public Health, which includes eight multidisciplinary healthcare clinics with sliding fee programs, and Rooted Santa Barbara, a community plant-based lifestyle organization. Cultural sensitivity focuses on delivering health information based on norms, values, beliefs, environmental factors, and historical context that is unique to a racial/ethnic population. Therefore, for our program to be culturally sensitive, it will include delivery of the program by CHWs primarily in the Spanish language with English as needed and incorporation of culturally relevant eating and physical activity recommendations. The specific aims of the project are: 1) in year one, develop the dietary-lifestyle behavioral intervention that encourages a plant-forward diet for pregnant Latina women with T2D to prevent excessive weight gain during pregnancy and improve blood sugar control in collaboration with CHWs and participants by conducting focus groups to incorporate feedback on the program; 2) initiate in year one, and in year two, conduct a randomized controlled trial with 30 pregnant Latina women with T2D to evaluate the how well the nutrition-behavior lifestyle program works; and 3) evaluate the acceptance and delivery of the dietary-lifestyle behavioral intervention in CHWs and participants. If successful, this study will establish the how well a culturally sensitive program delivered by CHWs incorporating plant-forward diets for pregnant Latina women with T2D prevents excessive weight gain during pregnancy, and control of blood sugar levels.

Interventions

BEHAVIORALNutrition-behavior lifestyle program

The 15 participants randomized to the intervention group will complete the activities described in the arm/group description.

Sponsors

Sansum Diabetes Research Institute
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

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

Inclusion criteria

* Diabetes in pregnancy * ≥ 18 years old * Self-reported Hispanic and/or Latino/a heritage * BMI ≥ 26.0 kg/m2 and ≤ 42.0 kg/m2

Exclusion criteria

* Type 1 Diabetes * Active substance abuse with alcohol or drugs by self-report * Treatment with non-diabetes medications (e.g., corticosteroids, anti-psychotics) known to have metabolic/body weight effects that could affect outcome measures * Non-singleton fetus * Evidence of fetal malformation * HbA1c ≥ 10% * Unable to provide informed consent or unwilling to complete the study

Design outcomes

Primary

MeasureTime frameDescription
Percent of glucose time in range assessed by using continuous glucose monitor30 days at baseline and at 27 weeks gestation, and at 35 weeks gestation.All participants will wear a Continuous Glucose Monitor for 30 days at three time points

Secondary

MeasureTime frameDescription
Amount of Gestational Weight Gainassessed at baseline and post-intervention (approximately 27-35 weeks gestation)weight gain in kilograms by measurements on a scale during study visits
Change in Blood Pressureassessed at baseline and post intervention (approximately 27-35 weeks gestation)systolic and diastolic blood pressure
Amount of satisfaction with the Interventionevaluated immediately post-interventionself-reported satisfaction satisfaction with the intervention assessed by surveys created for the purposes of this study

Countries

United States

Outcome results

None listed

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