Linking Temporal Patterns of Modifiable Behaviors to Weight Loss Outcomes
- Conditions
- ObesityWeight Change, Body
- Registration Number
- NCT03840733
- Lead Sponsor
- University of Colorado, Denver
- Brief Summary
This study is designed as an observational trial. The objective of this study is to follow-up with participants 3 years after completion of an 18-month comprehensive behavioral weight loss intervention. Outcomes of interest include change in body weight, body composition, physical activity, energy intake, and sleep. In addition, investigators will explore the associations between current physical activity, sleep, and energy intake patterns and body weight regulation.
- Detailed Description
A total of 170 participants were initially enrolled in the comprehensive behavioral weight loss intervention.In this study, investigators will conduct a follow-up visit 3 years after the completion of the intervention. Only participants who completed the behavioral weight loss intervention will be enrolled in this study. Participants will undergo testing of body weight, body composition, physical activity patterns, energy intake patterns, sleep patterns, resting metabolic rate, and total daily energy expenditure.
Recruitment & Eligibility
- Status
- ENROLLING_BY_INVITATION
- Sex
- All
- Target Recruitment
- 60
- Previous enrollment in standard behavioral weight loss intervention (NCT01985568 or NCT03411356)
- Age 20-60 (This age range has been selected based upon the participants enrolled in the Parent Trial)
- Capable and willing to give informed consent
- Possess a smartphone to install and utilize the meal timing application
- Capable and willing to wear the Actigraph, ActivPAL and Actiwatch-2 for 24 hours/day for 28 consecutive days
- Willing to complete the Total Daily Energy Expenditure (TDEE) assessment which includes multiple urine collections and drinking stable water isotopes
- Being considered unsafe to participate as determined by the study physician (Dr. Catennaci)
- New diagnosis of a medical condition (not observed in the Parent Trial) which may affect weight or energy metabolism (e.g. depression, CVD, diabetes, uncontrolled hypertension, untreated thyroid, renal, hepatic diseases)
- Women who became pregnant after completing the Parent Trial
- Current use or use within the last 6 months of prescription or over-the-counter medications known to affect appetite, weight, and sleep
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Weight Change Baseline to 54 months Change in body weight (kg)
Weight Maintenance 18 months to 54 months Change in body weight (kg)
Fat Mass Change Baseline to 54 months Change in Fat Mass (kg)
Fat Free Mass Change Baseline to 54 months Change in Fat Free Mass (kg)
Fat Free Mass Maintenance 18 months to 54 months Change in Fat Free Mass (kg)
Fat Mass Maintenance 18 months to 54 months Change in Fat Mass (kg)
- Secondary Outcome Measures
Name Time Method Change in Energy Intake 0, 6, 12, 18, 54 month Energy Intake patterns as measured by 3 day food record (kcal/day
Resting Metabolic Rate 54 month Resting metabolic rate as measured using indirect calorimetry (kcal/day)
Physical Activity Patterns 54 month Physical activity patterns as measured by ActivPAL, Actigraph (min/day)
Change in Sleep 0, 6, 12, 18, 24, 54 month Sleep patterns as measured by SenseWear armband (h/day)
Change in Physical Activity Patterns 0, 6, 12, 18, 24, 54 month Physical activity patterns as measured by SenseWear armband (min/day)
Sleep Patterns 54 month Sleep patterns as measured by Actiwatch-2, ActivPAL, Actigraph (h/day)
Energy Intake Patterns 54 month Energy Intake patterns as measured by 24 hour food recall and meallogger smartphone application (kcal/day)
Total Daily Energy Expenditure 54 month Total Daily Energy Expenditure as measured by doubly labeled water (kcal/day)
Physical Activity Energy Expenditure 54 month Physical Activity Energy Expenditure as measured by doubly labeled water (kcal/day)
Trial Locations
- Locations (1)
University of Colorado Anschutz Medical Campus
🇺🇸Aurora, Colorado, United States