Free healthy meals may rewire metabolism in Food-Insecure women
NCT ID NCT06800794
First seen Jun 24, 2026 · Last updated Aug 20, 2026 · Updated 4 times
Summary
This study looks at how not having reliable access to enough food might make it harder to lose weight. Researchers are giving 12 women who face food insecurity and have obesity and prediabetes a steady supply of healthy, low-calorie meals for a period. They will measure changes in weight, blood sugar, and how the body burns energy to see if a predictable diet can improve health and reduce cravings for unhealthy foods.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Behavioral skill training and meal provisioning (healthy, low-energy-dense meals delivered to home)
- What this could lead to
- If successful, this could point toward better weight management strategies for people facing food insecurity.
- What could go wrong
- This is a very small early study with only 12 participants, so results may not apply to everyone. It is designed to gather knowledge, not to test a treatment.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 12 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2025
- Expected to finish
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Sep 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 45 years
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Woman between the ages of 18-45. * Premenopausal. * Obese (BMI ≥ 30). * Diagnosed with prediabetes (HbA1c: 5.7%-6.4%). * Experiencing food insecurity (score of 2-6 on the six-item food insecurity questionnaire). * Income below 300% of the household federal poverty threshold. * Lives alone. Exclusion Criteria: * Actively planning to become pregnant (e.g., individuals trying to conceive or undergoing fertility treatment, based on self-report). * Delivered a baby within the past 6 months (self-report). * Non-ambulatory (e.g., individuals unable to walk independently or requiring a wheelchair for mobility). * Intellectual impairment that would impact treatment adherence. * Unmanaged mood disorders, substance use disorders, personality disorders, or a history of eating disorders, including: * Generalized anxiety disorder. * Depression. * Alcohol dependence. * Schizophrenia. * Anorexia nervosa, bulimia, or binge eating disorder within the past 6 months. * Recent weight loss exceeding 5% of body weight within the past 6 months (self-report). * Food allergies to study-related foods, including dairy, soy, nuts, or gluten. * History of bariatric surgery or GLP-1 agonist use (self-report). * Inability to read or write in English (self-report). * Planned relocation out of the study area during the study timeframe (self-report). * Uncontrolled diabetes (HbA1c \> 9%) or hypertension (blood pressure \> 160/100 mmHg), based on self-report or screening visit measurements.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Farber Hall G56
Buffalo, New York, 14221, United States
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