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Assessment of Outcomes Following Bariatric Surgery for Mississippi State Employees

Assessment of Outcomes Following Bariatric Surgery for Mississippi State Employees

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01162668
Enrollment
165
Registered
2010-07-14
Start date
2010-04-30
Completion date
2014-06-30
Last updated
2018-05-15

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

Conditions

Obesity

Keywords

bariatric surgery, obesity, outcomes

Brief summary

Objective: to assess the health and economic outcomes (weight lost, change in control of chronic diseases such as diabetes, quality of life, work productivity, health care cost, etc) associated with bariatric (weight-loss) surgery for 200 severely obese patients who undergo bariatric surgery as part of the Mississippi State Employees' Life and Health Insurance Plan's Obesity Treatment Program (OTP). 2\. Patient Characteristics: Inclusion criteria: Eligible bariatric surgical candidates who are enrolled in the OTP (100 patients per year for 2 years). The Plan's criteria includes, but is not limited to 1) enrollment in the plan for at least 12 consecutive months prior to September 1, 2009; 2) completion of the HealthQuotient health risk assessment through the Plan's wellness and health promotion program; 3) a Body Mass Index (BMI) of \>40 kg/m2, or a BMI \>35 kg/m2 with two or more co-morbidities such as diabetes, hypertension, sleep apnea or asthma; 4) two or more physician-supervised weight loss attempts within the last 24 months; 5) age 18 years or older; and 6) consent to provide personal and medical information to the Plan. Prior to surgery, each site administers a psychiatric evaluation to ensure the patient is psychologically stable for surgery. Exclusion criteria: any patient who does not meet criteria above or who declines to participate. Surgeries will take place only at Certified Bariatric Surgery Centers of Excellence (COE), of which, there are currently 3 in the state. The 3 COEs exist with 4 outpatient medical offices (1 COE is composed of 2 independent surgeon practices) Patients will be recruited at each site once they are approved by the OTP. 3\. Design: prospective, observational, multi-center, longitudinal study of outcomes and resource utilization associated with OTP. Estimates of obesity and comorbidities' impact will be obtained from the outpatient medical office for the COEs. Medical charts, databases and medical/pharmacy claims will be the source of information. Surveys on quality of life, productivity, and patient satisfaction will be administered directly to patients. Database claim information will be obtained in future and is not a part of current IRB application. 4: Procedures: After obtaining informed consent, patients will be administered surveys at baseline, as well as at follow-up visits. Additional data will be obtained via patient charts, databases, and medical/pharmacy claims.

Interventions

None listed

Sponsors

Allergan
CollaboratorINDUSTRY
University of Mississippi Medical Center
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Eligible bariatric surgical candidates who are enrolled in the Mississippi SSELHI Plan (100 candidates enrolled per year). The Plan's criteria includes, but is not limited to 1. enrollment in the plan for at least 12 consecutive months prior to September 1, 2009 2. completion of the HealthQuotient health risk assessment through the Plan's wellness and health promotion program 3. a Body Mass Index (BMI) of \>40 kg/m2, or a BMI \>35 kg/m2 with two or more co-morbidities such as diabetes, hypertension, sleep apnea or asthma 4. two or more physician-supervised weight loss attempts within the last 24 months 5. consent to provide personal and medical information to the Plan

Exclusion criteria

* Any patient who does not meet criteria above or who declines to participate.

Design outcomes

Primary

MeasureTime frameDescription
Body mass index (BMI)0, 6, 12, and 24 monthsChange in body mass index (BMI) from baseline
Weight loss0, 6, 12, and 24 monthschange in weight from baseline

Secondary

MeasureTime frameDescription
Systolic blood pressure0, 6, 12, and 24 monthschange in systolic blood pressure from baseline
Diastolic blood pressure0, 6, 12, and 24 monthschange in diastolic blood pressure from baseline
quality of life0, 6, 12, and 24 monthsImpact of weight on quality of life (IWQOL-lite) questionnaire; tool assesses 5 domains of quality of life: physical function, self-esteem, sexual life, public distress, and work impact
Work productivity0, 6, 12, and 24 monthsWork productivity and activity impairment questionnaire: General Health v2.0 (WPAI:GH) assesses work productivity
Medication use0, 6, 12, and 24 monthsChange in mean number of medications prescribed
ecomonic outcomes0, 6, 12, and 24 monthscosts to the insurance plan were assessed

Other

MeasureTime frameDescription
Surgery-related adverse events24 monthsAny surgery-related adverse events were noted

Countries

United States

Outcome results

None listed

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