Individualized Diet Improvement Program for Weight Loss and Maintenance, Cohort 2 (iDIP)

July 22, 2021 updated by: Mindy Lee, University of Illinois at Urbana-Champaign

Individualized Diet Improvement Program for Weight Loss and Maintenance

This research is to develop a weight loss and weight maintenance program through dietary modifications for adults with obesity. Although scientific studies have shown the feasibility of rapid and safe dietary weight loss and subsequent weight maintenance, no efficacious dietary weight management program is widely available, and thus bariatric surgery remains the most reliable approach for weight loss/management. Safe and effective dietary weight loss and subsequent weight maintenance require flexible, individualized advice by an experienced dietitian/nutritionist.

Study Overview

Status

Completed

Study Type

Interventional

Enrollment (Actual)

30

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Illinois
      • Urbana, Illinois, United States, 61801
        • University of Illinois at Urbana-Champaign

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 70 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

body mass index in the overweight or obese range (BMI) >28 kg/m2 (if Asian, BMI >25kg/m2); not currently pregnant or lactating; have Wi-Fi at home, a working email, and an iPhone or Android smartphone; no self-reported severe metabolic, cardiovascular or musculoskeletal disease; not using insulin injection; able to attend the 22 (1 hour) diet improvement sessions; willing to lose 20 lb. or more for 6 months and maintain a healthy weight for one year; keep weighing their weight for two years; fluent in reading and writing English.

Exclusion Criteria:

age <18 or >70 years; body mass index of <28 kg/m2 (if Asian, BMI <25kg/m2); currently pregnant; currently lactating; self-reported with severe metabolic, cardiovascular, or musculoskeletal disease; use insulin injection; not able to attend the 22 (1 hour) diet improvement sessions for 1 year; failed to set up a Wi-Fi scale; failed to submit a FFQ.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Weight Management Intervention
During a 12-month period, participants will attend a total of 22 diet improvement sessions, each of which will last approximately 1 hour. Twelve sessions will be held in the first 5 months and will be focused on safe and efficient weight loss. The participants will learn to create a personalized weight loss diet from their kitchen based on their diet practice and food preference. The next 10 sessions will be held in the last 7 months and will be focused on weight maintenance and healthy eating. The participants will build skills to select foods and create meals that prevent them from overeating. Participants will be followed by daily self-weighing for 1 year after intervention.
Participants attend group and individual dietary education sessions. Participants create a diet plan that satisfies their needs. Participants aim to lose 1 pound weekly until a BMI of 25 is reached. Participants are evaluated through daily self-weighing, dietary records, and food frequency questionnaires.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Body weight
Time Frame: Change from baseline (0 month) to 6 month, 12 month, 18 month, and 24 month
Body weight in kilograms measured on a standard scale (Withings, US)
Change from baseline (0 month) to 6 month, 12 month, 18 month, and 24 month

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Protein intake
Time Frame: Change from baseline (0 month) to 12 month
Protein intake in grams and grams/100 kilo-calories using a food frequency questionnaire (FFQ)
Change from baseline (0 month) to 12 month
Fiber intake
Time Frame: Change from baseline (0 month) to 12 month
Fiber intake in grams and grams/100 kilo-calories using a food frequency questionnaire (FFQ)
Change from baseline (0 month) to 12 month
Waist circumference
Time Frame: Change from baseline (0 month) to 6 month, 12 month, 24 month
Waist circumference in centimeters measured using a standard measuring tape
Change from baseline (0 month) to 6 month, 12 month, 24 month
Hip circumference
Time Frame: Change from baseline (0 month) to 6 month, 12 month, 24 month
Hip circumference in centimeters measured using a standard measuring tape
Change from baseline (0 month) to 6 month, 12 month, 24 month
Body composition
Time Frame: Change from baseline (0 month) to 6 month, 12 month, 24 month
Body fat measured using InBody 270
Change from baseline (0 month) to 6 month, 12 month, 24 month
Body composition
Time Frame: Change from baseline (0 month) to 6 month, 12 month, 24 month
muscle mass measured using InBody 270
Change from baseline (0 month) to 6 month, 12 month, 24 month
Protein intake
Time Frame: Periodically from baseline (0 month) to 12 month
Protein intake in grams and grams/100 kilo-calories using a 24-hour dietary record
Periodically from baseline (0 month) to 12 month
Fiber intake
Time Frame: Periodically from baseline (0 month) to 12 month
Fiber intake in grams and grams/100 kilo-calories using a 24-hour dietary record
Periodically from baseline (0 month) to 12 month

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 26, 2019

Primary Completion (Actual)

April 10, 2021

Study Completion (Actual)

April 10, 2021

Study Registration Dates

First Submitted

October 26, 2020

First Submitted That Met QC Criteria

October 27, 2020

First Posted (Actual)

October 28, 2020

Study Record Updates

Last Update Posted (Actual)

July 23, 2021

Last Update Submitted That Met QC Criteria

July 22, 2021

Last Verified

July 1, 2021

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 18069_cohort2

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Obesity

Clinical Trials on Weight Management Intervention

3
Subscribe