Feasibility of Integrating Indirect Calorimetry (IC) Technology in Primary Care
Feasibility Study of Integrating IC Technology With the WatchWT Comprehensive Weight Reduction Program.
1 other identifier
interventional
75
1 country
1
Brief Summary
The purpose of this study is to evaluate the feasibility of using indirect calorimetry (IC) within a comprehensive weight reduction program. Will individuals that receive a personalized nutrition program, at baseline, from IC technology respond better to treatment compared to individuals receiving IC technology at three months.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable obesity
Started Jan 2008
Shorter than P25 for not_applicable obesity
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2008
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2008
CompletedStudy Completion
Last participant's last visit for all outcomes
September 1, 2008
CompletedFirst Submitted
Initial submission to the registry
September 9, 2008
CompletedFirst Posted
Study publicly available on registry
September 10, 2008
CompletedSeptember 21, 2009
September 1, 2009
8 months
September 9, 2008
September 18, 2009
Conditions
Outcome Measures
Primary Outcomes (1)
Bodyweight
Six Months
Secondary Outcomes (4)
Psychobehavioral: Self-Efficacy
Six Months
Quality Life
Six Months
Blood Pressure
Six Months
Eating Behavior
Six Months
Study Arms (2)
E1
EXPERIMENTALA1
ACTIVE COMPARATORInterventions
Individuals will receive IC measurement at baseline and three months. Nutrition and physical activity plan will be developed and adjusted from measured RMR and lifestyle.
Individuals will receive standard dietary plan. Women will receive 1200 Kcal/day and men will receive 1600 Kcal/day. Individuals will receive RMR measurement at three months. RMR information will be used to help improve eating behavior.
Eligibility Criteria
You may qualify if:
- BMI greater than 30 kg/m2
- years of age
You may not qualify if:
- No participation in other weight loss efforts outside study.
- Pregnant or lactating
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Colorado Center for Chronic Care Innovations
Westminster, Colorado, 80031, United States
Related Publications (1)
McDoniel SO, Wolskee P, Shen J. Treating obesity with a novel hand-held device, computer software program, and Internet technology in primary care: the SMART motivational trial. Patient Educ Couns. 2010 May;79(2):185-91. doi: 10.1016/j.pec.2009.07.034. Epub 2009 Aug 20.
PMID: 19699049DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
September 9, 2008
First Posted
September 10, 2008
Study Start
January 1, 2008
Primary Completion
September 1, 2008
Study Completion
September 1, 2008
Last Updated
September 21, 2009
Record last verified: 2009-09