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Sustainable Weight Loss Study: Nutrition Support Tools and Weight Loss Among Obese People

Sustainable Weight Loss Study: Nutrition Support Tools and Weight Loss Among Obese People

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04378322
Enrollment
300
Registered
2020-05-07
Start date
2020-05-04
Completion date
2022-07-31
Last updated
2020-05-07

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

Conditions

Obesity

Keywords

weight loss, digital, nutrition, healthy eating, food purchasing, meal planning, obese, online, MyPlate

Brief summary

The purpose of this research study is to determine the effectiveness of nutrition tools to support weight loss among obese individuals. All participation will be based online and there will be no in-person visits. Participants will be given nutrition support tools for 6 months. Participants will be asked to report their weight and diet at the start of the study, and every month for 6 months during the study period. Participants will additionally be asked to report weight and diet at 12 months, 18 months, and 24 months after the start of the study. Total study duration will be 2 years.

Detailed description

Obesity is a major public health burden. Weight loss among obese participants may improve future health outcomes and financial burden to the healthcare system and employers. The effect of personalized meal planning and online food purchasing and delivery on weight loss and management is unknown. Design: This trial is an online, three-arm randomized trial to compare a meal planning and telenutrition tool, a meal planning tool only, and MyPlate optimization. Participants will be assigned to randomly assigned in a 1:1:1 ratio to one of the three groups. Participants will follow the intervention for 6 months after randomization and will be followed for an additional 1.5 years after randomization. Participants will report dietary behavior and weight at baseline and each month of the intervention (6 months), 12 months, 18 months, and 24 months. Population Approximately 300 participants will be enrolled and randomized (100 per arm). Participants will be adults living in New York state who are obese (at least a BMI of 30 kg/m2). Outcomes Primary outcome: weight change after 6 months Other outcomes: waist circumference; blood pressure, dietary changes, cooking, meal planning, and eating out frequencies

Interventions

BEHAVIORALNutrition and food purchasing tool + telenutrition

Participants will be asked to use a meal planning and food purchasing feature regularly (at least once every two weeks) and schedule appointments with a registered dietitian.

BEHAVIORALNutrition and food purchasing tool

Participants will be asked to use a meal planning and food purchasing feature regularly (at least once every two weeks).

BEHAVIORALNutrition education tool

Participants will be asked to review nutrition education materials online.

Sponsors

Zipongo
Lead SponsorINDUSTRY

Study design

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

Eligibility

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

Inclusion criteria

BMI ≥ 30 kg/m2 Male or female 18 or older Non-institutionalized Able and willing to provide informed consent Willing to change diet for 3 months Has access to a scale to weigh themselves Lives in NY state

Exclusion criteria

Refuse or are unable to provide informed consent to participate in the study Undergoing active cancer treatment Has type 1 or 2 diabetes Stage 3+ CKD or kidney failure Are pregnant or breastfeeding, have given birth in the last three months, or are planning to be pregnant in the next 3 months Report of congestive heart failure Diagnosed with an eating disorder (e.g. anorexia nervosa or bulimia nervosa) Current or former Zipongo users

Design outcomes

Primary

MeasureTime frameDescription
Weight changeBaseline and end of months 1, 2, 3, 4, 5, 6, 12, 18, and 24Weight will be measured using a scale and self-reported.

Secondary

MeasureTime frameDescription
Waist circumferenceBaseline and end of months 1, 2, 3, 4, 5, 6, 12, 18, and 24Waist circumference will be measured using a tape measure and self-reported.
Blood pressureBaseline and end of months 1, 2, 3, 4, 5, 6, 12, 18, and 24Blood pressure will be a self-reported assessment at a clinic or pharmacy.
Change in diet qualityBaseline and end of months 1, 2, 3, 4, 5, 6, 12, 18, and 24Diet quality will be assessed using a food frequency questionnaire.

Outcome results

None listed

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