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Relationship of Realize Mysuccess Usage to Outcomes of Bariatric Surgery

Relationship of Realize Mysuccess Usage to Outcomes of Bariatric Surgery

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01197937
Enrollment
25000
Registered
2010-09-09
Start date
2010-08-31
Completion date
2012-07-31
Last updated
2013-12-11

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

Conditions

Bariatric Surgery, Obesity, Weight Loss

Brief summary

The goal of this observational study is to assess the efficacy of Realize My Success (RMS),a website that allows patients and providers to maintain contact via the website. We will compare RMS users on a number of different variables with the goal of identifying which variables are associated with optimal outcomes (larger weight losses) at one year (and potentially beyond). The study has two primary objectives. The first is to assess changes in body weight at postoperative year 1 in frequent v. infrequent RMS users. We predict that frequent users will achieve significantly greater reductions in weight at 6 and 12 months (and beyond) than infrequent users. The second objective is to assess changes in body weight at postoperative year 1 in persons who use different features of the RMS site. We hypothesize that persons who, on a regular basis, record their food intake, track their physical activity and make specific behavioral goals will experience significantly greater reductions in weight beginning 6 months after surgery as compared to those who do not use these features of the RMS site.

Interventions

None listed

Sponsors

Ethicon Endo-Surgery
CollaboratorINDUSTRY
University of Pennsylvania
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* 18-65 years old * BMI between 40-70 kg/m2 (or 35-70 kg/m2 in the presence of co-morbidities) * Have registered in the Realize Mysuccess Systema and have logged into the system at least once postoperatively.

Exclusion criteria

* We will be receiving/analyzing a data set based on the inclusion criteria, therefore there is no set

Design outcomes

Primary

MeasureTime frame
Assess changes in body weight in frequent v. infrequent RMS users12 months

Outcome results

None listed

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