Evaluation of a Weight Management Program
This study has been completed.
Sponsor:
Nestlé
Information provided by (Responsible Party):
Nestlé
ClinicalTrials.gov Identifier:
NCT00888251
First received: April 24, 2009
Last updated: September 21, 2011
Last verified: September 2011
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Purpose
This retrospective chart review and data abstraction will evaluate and quantify the effectiveness of a comprehensive weight management program. The hypothesis is that the program will positively affect weight, weight-related comorbidities and medication use.
| Condition | Intervention |
|---|---|
|
Obesity |
Other: Comprehensive weight management program |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Retrospective |
| Official Title: | A Multicenter, Retrospective Study to Evaluate the Effectiveness of the OPTIFAST Weight Management Program |
Resource links provided by NLM:
Further study details as provided by Nestlé:
| Enrollment: | 153 |
| Study Start Date: | March 2009 |
| Study Completion Date: | July 2009 |
| Primary Completion Date: | July 2009 (Final data collection date for primary outcome measure) |
| Groups/Cohorts | Assigned Interventions |
|---|---|
| Comprehensive weight management program |
Other: Comprehensive weight management program
Full meal replacement, behaviorial modification, medical monitoring, exercise.
Other Name: OPTIFAST Program
|
Eligibility| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
Study Population
OPTIFAST Program participants
Criteria
Inclusion Criteria:
- Records of the first 40 study center participants who enrolled in the OPTIFAST Program from January 1, 2006 through June 30, 2006
- Records of subjects who completed the active weight loss phase of the program
- Records where data is available through the transitional phase of the program
Exclusion Criteria:
- Concurrent use of appetite suppressants or other weight loss medications
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00888251
Locations
| United States, Indiana | |
| Lutheran Weight Management Center | |
| Fort Wayne, Indiana, United States, 46804 | |
| United States, Iowa | |
| Mercy Center for Weight Reduction | |
| Des Moines, Iowa, United States, 50309 | |
| United States, Michigan | |
| Sparrow Weight Management Center | |
| East Lansing, Michigan, United States, 48823 | |
| United States, Ohio | |
| Jewish Hospital Weight Management Center | |
| Cincinnati, Ohio, United States, 45236 | |
Sponsors and Collaborators
Nestlé
More Information
No publications provided
| Responsible Party: | Nestlé |
| ClinicalTrials.gov Identifier: | NCT00888251 History of Changes |
| Other Study ID Numbers: | 08.27.CLI |
| Study First Received: | April 24, 2009 |
| Last Updated: | September 21, 2011 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by Nestlé:
|
Obesity Meal replacement Obesity treatment Weight management |
Additional relevant MeSH terms:
|
Obesity Overnutrition Nutrition Disorders |
Overweight Body Weight Signs and Symptoms |
ClinicalTrials.gov processed this record on May 19, 2013