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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04605653
Other study ID # 18069_cohort1
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 23, 2018
Est. completion date July 28, 2019

Study information

Verified date November 2020
Source University of Illinois at Urbana-Champaign
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Completed
Enrollment 14
Est. completion date July 28, 2019
Est. primary completion date July 28, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 64 Years
Eligibility Inclusion Criteria: - body mass index (BMI) >28 kg/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 one and a half years; - fluent in reading and writing English. Exclusion Criteria: - age <18 or >64 years; - body mass index of <28 kg/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 Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Weight Management 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.

Locations

Country Name City State
United States University of Illinois at Urbana-Champaign Urbana Illinois

Sponsors (1)

Lead Sponsor Collaborator
University of Illinois at Urbana-Champaign

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Body weight Body weight in kilograms measured on a standard scale (Weight Gurus, Greater Goods LLC, MO) Change from baseline (0 month) to 6 month, 12 month, and 18 month
Secondary Waist circumference Waist circumference in centimeters measured using a standard measuring tape Change from baseline (0 month) to 12 month
Secondary Hip circumference Hip circumference in centimeters measured using a standard measuring tape Change from baseline (0 month) to 12 month
Secondary Protein intake Protein intake in grams and grams/100 kilo-calories using a food frequency questionnaire (FFQ) Change from baseline (0 month) to 12 month
Secondary Protein intake Protein intake in grams and grams/100 kilo-calories using a 24-hour food record Periodically from baseline (0 month) to 12 month
Secondary Fiber intake Fiber intake in grams and grams/100 kilo-calories using a food frequency questionnaire (FFQ) Change from baseline (0 month) to 12 month
Secondary Fiber intake Fiber intake in grams and grams/100 kilo-calories using a 24-hour food record Periodically from baseline (0 month) to 12 month
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