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PASO A PASO: Tailored Diabetes Prevention Program for Spanish-Speaking Communities Feasibility Study

PASO A PASO Pilot Study: Tailored Diabetes Prevention Program for Spanish-Speaking Communities Feasibility Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07392008
Enrollment
45
Registered
2026-02-06
Start date
2025-07-01
Completion date
2026-03-31
Last updated
2026-02-06

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

Conditions

Pre Diabetic

Keywords

feasibility, Spanish-speaking populations, diabetes prevention adaptation

Brief summary

The interdisciplinary and interprofessional community-academic partnership (CAP) has been working with Spanish-speaking H/L Salt Lake City residents and organization leaders to adapt the National Diabetes Prevention Program to meet the needs of this population. This next collaboration phase attempts to finalize the adapted diabetes prevention program, "Paso a Paso," and evaluate its feasibility and implementation strategies. The purpose of this pilot study is to inform the necessary modifications to the Paso a Paso diabetes prevention intervention, ensuring that the full-scale future intervention is both feasible and effective for the target community.

Detailed description

Specific goals include: 1. Finalize the adapted "Paso a Paso" protocol and materials. 2. Train the first cohort of instructors for the program (10-15 potential instructors) 3. Test the feasibility of the intervention implementation with 30 community participants. 4. Gather feedback from participants, refine the intervention, and ensure that it resonates with community members, ultimately laying the foundation for a successful larger study.

Interventions

BEHAVIORALPaso a Paso

Cultural components will include fostering a sense of belonging, collaboration, support, interaction, and respect. Program structure: Paso a Paso is designed to include weekly 90-minute in-person sessions over the first 4 months of the program, which will transition to monthly sessions over the final 8 months of the intervention. All sessions will include hands-on skill development, group and social activities, and addressing assets for diabetes prevention available in the community. Finally, the intervention also includes an online community forum to support ongoing social support and information provision.

Sponsors

University of Utah
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

Feasibility and pilot study

Eligibility

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

Inclusion criteria

Native Spanish speakers, residents in the Wasatch Front Metropolitan area, adults aged \>18 years old with a BMI of ≥ 25, and diabetes risk \>1 based on the CDC Prediabetes Risk Test

Exclusion criteria

1. Bariatric surgery in the last 2 years or planned during the next year 2. Edematous state that interferes with body weight assessment (e.g., severe congestive heart failure, end-stage renal disease, or ascites) 3. Current or planned pregnancy in the next year 4. Current breastfeeding

Design outcomes

Primary

MeasureTime frameDescription
Weight percent changeBaseline, 4-month, 12-month (exploratory)Will be measured in kilograms using a calibrated Tanita WB-100A scale.

Secondary

MeasureTime frameDescription
% HbA1cBaseline, 4-month, 12-month (exploratory)HbA1c will be tested using Point-of-Care (POC) A1c testing, which will require a finger prick.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORMolly B Conroy, MD, MPH

University of Utah

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 7, 2026