RECRUITING

Adaptive Responses to Overfeeding and Weight

Conditions

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

To more effectively address the problem of weight regain following weight loss for obese individuals, this study will evaluate the underlying biology of the reduced obese state. In depth studies of appetite, energy expenditure, physical activity levels and fat metabolism will be completed in obese and reduced obese individuals; with the latter subdivided into those who have lost weight with diet alone or diet plus exercise. Individuals will be studied following a brief overfeeding period to better understand how differences in biological responses to overeating might be involved in promoting or protecting against weight gain.

Official Title

Adaptive Responses to Overfeeding and Weight Regain in Reduced Obese Individuals

Quick Facts

Study Start:2019-02-15
Study Completion:2024-01-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT03857048

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.

Ages Eligible for Study:30 Years to 50 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. Age 18 years or older
  2. Willing and able to provide informed consent
  3. Able to understand and follow study procedures
  4. Stable medical condition
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Study Contact

Sheila Steinke, MS
CONTACT
303.724.3304
sheila.steinke@cuanschutz.edu
Emilee Mickaliger, BS
CONTACT
emilee.mickaliger@cuanschutz.edu

Principal Investigator

Daniel Bessesen, MD
PRINCIPAL_INVESTIGATOR
University of Colorado Anschutz Health and Wellness Center

Study Locations (Sites)

University of Colorado Hospital
Aurora, Colorado, 80045
United States

Collaborators and Investigators

Sponsor: University of Colorado, Denver

  • Daniel Bessesen, MD, PRINCIPAL_INVESTIGATOR, University of Colorado Anschutz Health and Wellness Center

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 Registration Dates

Study Start Date2019-02-15
Study Completion Date2024-01-01

Study Record Updates

Study Start Date2019-02-15
Study Completion Date2024-01-01

Terms related to this study

Additional Relevant MeSH Terms

  • Obesity