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

Obesity Clinical Trial

Official title:

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

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT04378322
• Other study ID #: 102
• Status: Not yet recruiting
• Phase: N/A
• Start date: May 4, 2020
• Est. completion date: July 2022

Study information

• Verified date: May 2020
• Source: Zipongo
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

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

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 300
• Est. completion date: July 2022
• Est. primary completion date: December 2020
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

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

Related Conditions & MeSH terms

• Obesity
• Weight Loss

Intervention

Behavioral:
• Nutrition 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.
• Nutrition and food purchasing tool
Participants will be asked to use a meal planning and food purchasing feature regularly (at least once every two weeks).
• Nutrition education tool
Participants will be asked to review nutrition education materials online.

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Zipongo

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Weight change	Weight will be measured using a scale and self-reported.	Baseline and end of months 1, 2, 3, 4, 5, 6, 12, 18, and 24
Secondary	Waist circumference	Waist circumference will be measured using a tape measure and self-reported.	Baseline and end of months 1, 2, 3, 4, 5, 6, 12, 18, and 24
Secondary	Blood pressure	Blood pressure will be a self-reported assessment at a clinic or pharmacy.	Baseline and end of months 1, 2, 3, 4, 5, 6, 12, 18, and 24
Secondary	Change in diet quality	Diet quality will be assessed using a food frequency questionnaire.	Baseline and end of months 1, 2, 3, 4, 5, 6, 12, 18, and 24