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The Short-Term Effect of a Technology Driven Weight Control (SMART) Program for Obese Adults

Phase I Study of Integrating RMR Technology and Email Counseling in a PCP Office.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00624598
Acronym
WCPC
Enrollment
110
Registered
2008-02-27
Start date
2008-01-31
Completion date
2008-08-31
Last updated
2008-09-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity, Hypertension

Brief summary

The purpose of this study is to evaluate the short-term effect of a technology based weight reduction program for obese (BMI \> 30 kg/m2) adults in a primary care office.

Interventions

BEHAVIORALSMART

Use of measured resting metabolic rate from indirect calorimetry for personalized diet program and use of a computer application for journalizing food and exercise.

Sponsors

Microlife
CollaboratorINDUSTRY
Colorado Center for Chronic Care Innovations, Inc.
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

1. Participant between the ages of 18-65 years. 2. Participant with a BMI (Body Mass Index \> 30.0 kg/m2) 3. Have access and use email a minimum of 2-days per week.

Exclusion criteria

1. Participant is not pregnant or lactating: Weight loss is not recommended for pregnant women and extra energy requirements are essential for fetal development (Butte, Wong, Treuth, Ellis, & O'Brian Smith, 2004; Durnin, 1991). 2. Participant is not currently participating in any structured/self-help weight loss program. The elimination of individuals actively participating in a current weight loss program will reduce the potential of a carry-over effect from these weight loss modalities (Fife-Shaw, 2006). 3. Participant has not attempted weight loss in the past 3 months. Same as number two.

Design outcomes

Primary

MeasureTime frame
Individuals receiving a technology-based weight reduction program will not have a significant increase in psychosocial constructs (i.e. weight self-efficacy, perceived behavioral control, attitude) compared to control group.10 weeks
Individuals receiving a technology-based weight reduction program will not improve eating behaviors (i.e. dietary cognitive restraint, emotional eating, uncontrolled eating) compared to control group.10 weeks
Individuals receiving a technology-based weight reduction program will not lose significantly more weight compared to control group.10 weeks
Individuals receiving a technology-based weight reduction program will not significantly improve systolic and diastolic blood pressure compared to control group(controlled for Bp medications).10 Weeks

Secondary

MeasureTime frame
Individuals receiving a technology-based weight reduction program will not significantly improve weight quality of life compared to control group.10 weeks
There is no relationship between psychosocial values (i.e. weight self-efficacy, weight perceived behavioral control, weight attitude) and eating behaviors (i.e. dietary cognitive restraint, uncontrolled eating, and emotional eating).10 Weeks

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026