Actively Recruiting

Phase Not Applicable
Age: 18Years - 40Years
All Genders
Healthy Volunteers
NCT06230744

A Novel Intervention for Weight Loss in Young Adults

Led by University of Chicago · Updated on 2025-11-17

140

Participants Needed

1

Research Sites

207 weeks

Total Duration

On this page

Sponsors

U

University of Chicago

Lead Sponsor

N

Northwestern University

Collaborating Sponsor

AI-Summary

What this Trial Is About

Obesity and cardiometabolic risks are significant public health issues, with about two-thirds of U.S. adults overweight or obese. Weight loss can prevent these health problems, but current lifestyle interventions have limited success. New, effective strategies are needed to address this rising issue at the population level. The goal of this clinical trial is to investigate how a behavioral intervention combined with technology impacts weight loss in young adults. The main questions it aims to answer are: • How does the combination of behavioral intervention and technology influence weight loss in young adults?

CONDITIONS

Official Title

A Novel Intervention for Weight Loss in Young Adults

Who Can Participate

Age: 18Years - 40Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Overweight or obese (BMI 25.5-34.9 kg/m2) men and women
  • Ages 18 to 40 years
  • Weight stable (no change >25 lbs in the past 3 months)
  • Owns a smartphone and willing to install the study app
Not Eligible

You will not qualify if you...

  • Presence of obstructive sleep apnea or other sleep disorders
  • Irregular menses, menopausal symptoms, post-menopausal, currently pregnant, trying to get pregnant or nursing
  • Regular travel across time zones
  • Currently following a weight loss regimen or special diet or exercise program
  • Increased fractional lean body mass (e.g., athletes)
  • Unable to walk, using an assistive device for mobility, or contraindications to exercise
  • Diabetes
  • Claustrophobia
  • Excessive alcohol (>2 drinks/day), caffeine (>300mg/day) intake, regular nicotine use, or substance abuse
  • Abnormal screening blood test results
  • Taking prescription or over-the-counter drugs/supplements affecting sleep or weight
  • Major psychiatric or eating disorders
  • Acute or chronic medical conditions increasing intervention risks, including heart disease (unstable angina, recent hospitalization for heart failure, significant arrhythmias), pulmonary disease needing oxygen or bronchodilators, recent cancer treatment unless prognosis is good, active infections, thyroid/endocrine disorders, hepatitis or chronic gastrointestinal disease, renal disease, significant anemia
  • Recent or significant abdominal surgery
  • Acute coronary syndrome or stroke within past 6 months

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Chicago

Chicago, Illinois, United States, 60637

Actively Recruiting

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Research Team

O

Olivia Hughes

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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