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Assessment of an Intervention to Prevent Obesity and Diabetes in Latino Farm Workers

Pasos Saludables: A Pilot Intervention to Prevent Obesity and Diabetes Among Latino Farm Workers

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01855282
Acronym
Pasos
Enrollment
254
Registered
2013-05-16
Start date
2010-04-30
Completion date
2011-04-30
Last updated
2017-05-15

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

Conditions

Overweight and Obesity

Keywords

Diabetes Type II,, Overweight,, Obesity,, Behavioral Intervention,, Latino, farm worker, randomized controlled intervention

Brief summary

This is a study to assess the effectiveness of a culturally appropriate behavioral intervention to reduce obesity levels and ultimately the risk of developing diabetes type II in immigrant Latino farm workers. Workers enrolled in a 2:1 ratio by random allocation into an intervention or control arm of the study. The intervention participants received weekly classes for 10 weeks with education on diabetes, diet and physical activity and practical exercises. Both control and intervention were measured for weight, waist circumference, fasting blood glucose and interviewed before and after the study intervention. The main hypothesis was that intervention, but not control participants, would experience reduction in body measurements after the intervention.

Detailed description

A more detailed description is not desired as noted above.

Interventions

BEHAVIORALBehavioral Intervention

Intervention participants attended up to 10 educational sessions teaching them about diabetes, and modifiable lifestyle factors (behaviors) to reduce the risk of diabetes by controlling weight. Sessions were conducted by Promotoras using culturally sensitive and appropriate materials and themes. Group activities and support were also emphasized. The control participants like the intervention were measured and interviewed before and again after the intervention sessions, but received no educational instruction or materials.

Sponsors

University of California, Davis
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Aged 18 -60 * BMI between 20 -38 * Willing to attend 10 weekly education sessions * Able to speak and understand Spanish * Have medical insurance

Exclusion criteria

* Fasting blood glucose about 126mg/dL unless physician attests fit to participate * Pregnancy or trying to conceive, or breastfeeding * Diabetic * On therapeutic diets * On medications that affect weight * If spouse / cohabitant already in the study * Not a farm worker working for the Reiter Affiliated Companies

Design outcomes

Primary

MeasureTime frameDescription
Change in BMIBefore intervention and after (12-14 weeks after first assessment)Weight and Height assessed for both control and intervention participants before intervention program and then assessed 2-3 weeks after the intervention period completed.

Secondary

MeasureTime frameDescription
Change in Waist CircumferenceMeasured before and after intervention (12 - 13 weeks after first assessmentWaist circumference measured in both control and intervention participants using a standard protocol. Conducted before intervention started and again 2-3 weeks after the intervention sessions finished.

Other

MeasureTime frameDescription
Change in fasting blood glucoseMeasured before intervention and after (12-13 weeks after first assessment)Fasting blood glucose was a voluntary assessment and therefore not conducted in all participants. Blood glucose was assessed from a middle digit using a sterile lancet and Accu-Check Advantage Blood Glucose Meter. It was assessed before the start of the intervention and after completion in both controls and intervention participants.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 15, 2026