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De Por Vida: A Diabetes Risk Reduction Intervention for Hispanic Women

NCT03113916 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 195

Last updated 2020-09-23

Study results available
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Summary

This pragmatic randomized clinical trial will assess the efficacy, cost, and sustainability of a culturally tailored weight-loss program targeting obese Hispanic women with pre-diabetes or T2D. The intervention will be integrated into patient care at a Federally Qualified Health Center serving over 30,000 low-income patients, and will be delivered by trained clinic staff, with minimal support from research staff. After the effectiveness clinical trial, two cohorts of clinic patients will receive the intervention in a sustainability test.

Conditions

Interventions

BEHAVIORAL

Behavioural Lifestyle Intervention

A culturally tailored behavioral intervention.

Sponsors & Collaborators

  • Arizona State University

    collaborator OTHER

  • Kaiser Permanente

    lead OTHER

Principal Investigators

  • Nangel Lindberg, PhD · Kaiser Permanente

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2014-06-23
Primary Completion
2018-03-05
Completion
2018-03-05

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03113916 on ClinicalTrials.gov