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The $Ensible Weight Program: An Intervention Tailored for Low Income Women

The $Ensible Weight Program: An Intervention Tailored for Low Income Women

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02251587
Enrollment
28
Registered
2014-09-29
Start date
2014-09-30
Completion date
2015-12-31
Last updated
2016-02-03

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

Conditions

Weight Loss

Brief summary

The purpose of this study is to learn if a weight loss program especially designed to address food insecurity is more effective compared to a standard weight loss program.

Detailed description

Low income women are at greater risk of both obesity and food insecurity (not having consistent access to nutritious and adequate amounts of food). Most weight loss programs targeted at low income women do not focus on gaining skills and knowledge to reduce food insecurity. Eligible participants will be randomized into one of two groups. The two groups will follow different weight management programs. One group will follow a standard weight management program. The other group with follow the investigations program, the $ensible Weigh Program. Participation in the study will last about 9 months.

Interventions

OTHERStandard Weight Management Program

Standard Diet program based on diet and exercise.

OTHERSensible Weigh Program

Weight loss program designed for low income women.

Sponsors

Jeannine Goetz, PhD
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
21 Months to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Documented low income * Body Mass Index (BMI) \>25.0 kg/m2 * Must speak and understand English * Able to attend intervention sessions and have access to telephone

Exclusion criteria

* Report serious medical risk such as insulin-dependent diabetes, cancer, recent cardiac event * Currently or planning to become pregnant during the intervention * Have no control over food purchases or choices * Report participation in a weight reduction program involving diet or PA within past 6 months * Report symptomology of an eating disorder * Report adherence to specialized diet regimes, i.e., multiple food allergies, vegetarian, Atkins, macrobiotic, etc.

Design outcomes

Primary

MeasureTime frameDescription
Feasibility of implementing weight management program9 MonthsFeasibility assessed by participant retention, participant attendance at study related visits, and participant satisfaction.

Secondary

MeasureTime frameDescription
Change in weightChange from Baseline to Month 3Change in weight during the weight loss phase
Change in diet qualityChange from Baseline to Month 3Change during the weight loss phase. Change will be measured based on questions answered about participant's diet quality. Changes measured based on lower percentage of calories from fat and increased consumption of fruits, vegetables and whole grains.
Change in food security statusChange from Baseline to Month 3Change during the weight loss phase. Change will be measured based upon responses to the US Household Food Security Questionnaire

Countries

United States

Outcome results

None listed

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