Loss - Louisiana Obese Subjects Study
试验速览
- 阶段
- 4 期
- 状态
- 终止
- 入组人数
- 390
- 试验地点
- 1
- 主要终点
- Percent Change From Baseline Weight
研究概览
简要总结
LOSS is a pragmatic clinical evaluation of intensive medical approaches to weight loss for individuals with extreme obesity (body mass index [BMI] 40-60 kg/m2). The intensive medical treatment is designed to produce 25% weight loss from baseline and to maintain at least 20% weight loss from baseline. The intensive medical treatment is compared to a usual care treatment model where individuals utilize self directed approaches to weight loss. The active treatment period is three years, followed by two years of observation.
详细描述
LOSS is a pragmatic clinical trial designed to evaluate intensive medical treatment for patients with severe obesity who would otherwise qualify as candidates for obesity surgery and who are covered by the Louisiana Office of Group Benefits (OGB) Health Insurance. LOSS will track the efficacy, safety and costs to compare two patient management approaches - intensive medical treatment, or a usual medical care treatment model. Recruitment will be done by mailers to insured patients to identify eligible candidates. We will randomly assign eligible volunteers to intensive medical treatment (n=240) or usual care (n=240). Patients will be evaluated annually and medical treatments are given in eight clinics around Louisiana. The eight sites are in Alexandria, Baton Rouge, Lafayette, Lake Charles, Monroe, Hammond, New Orleans and Shreveport.
Hypothesis:
We hypothesize that we can achieve weight loss after two and five years that exceeds 20% from baseline with intensive medical management of persons with class III obesity and that this weight loss is greater than that achieved with usual medical care including access to a weight management web site.
Our secondary hypotheses are: 1) that the weight loss at year 2 and 5 in the intensive medical group is associated with improvements in blood pressure, fasting glucose, lipids, health-related quality of life and psychosocial measures and is greater improvement than that achieved with usual medical care and access to a website; and 2) that total medical costs in the intensive medical management group will compare favorably to total medical costs in the usual care group (i.e., total reimbursement from insurance costs will be less, even when the expense of the treatment is considered).
Overall Aim:
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 20 Years 至 60 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Participant in the Exclusive Provider Organization (EPO), Managed Care Organization (MCO) and Preferred Provider Organization (PPO) programs of the Louisiana State Employees Group Benefits Health Insurance
- •Agree to travel for treatment to the assigned study site
- •Agree to randomized treatment assignment
- •Male and females age 20-60 years
- •Body Mass Index >40kg/m2 but < 60 kg/m2
- •Females must be non-pregnant and using an approved contraception method
- •Complete Blood Count (CBC): normal hematocrit, white count and platelet count, unless waived by Principal Investigator (PI)
- •Uric Acid <9.0 mg/dl
- •Normal Creatinine
- •Normal Thyroid Stimulating Hormone (TSH)
- •Negative urine pregnancy test for women of childbearing potential
- •Able to give written informed consent
- •Able to comply with study procedures
排除标准
- •Factors that may limit adherence to interventions or affect conduct of the trial:
- •Unable or unwilling to give informed consent or communicate with local study staff
- •Hospitalization for psychiatric illness or substance use/abuse within the past year
- •Self-report of alcohol or substance abuse within the past twelve months
- •Current major depressive episode or history of suicidal behaviors
- •Endorsement of significant recent suicidal ideation (as determined by PI)
- •Travel plans that do not permit participation
- •History of prior bariatric surgery, small bowel resection, or extensive bowel resection
- •Current use of chronic systemic corticosteroids, appetite suppressants, antipsychotic medication, herbal medications for weight loss or any medication not approved by the PI.
- •Another member of the household is a participant or staff member in the study
- •History of eating disorder such as anorexia nervosa, bulimia, or binge eating
- •Diagnosis of schizophrenia, other psychotic disorders, bipolar disorder, or personality disorder (as determined by the PI)
- •Currently pregnant or nursing or plans to become pregnant in the next five years
- •Except for non-melanoma skin cancer, cancer requiring treatment in the past five years, unless the prognosis is excellent
- •Self report of Human Immunodeficiency Virus (HIV) positive, hepatitis C or active tuberculosis
- •Cardiovascular disease event within the past year
- •Severe congestive heart failure (New York Heart Association [NYHA] Functional Class III, IV)
- •Second degree or greater heart block
- •Blood Pressure >160 systolic or >100 diastolic on two consecutive visits, unless treated and re-screened
- •Based upon responses to psychological screening or an interview, patients may be excluded by the study psychologist.
- •Other medical, psychiatric, or behavioral limitations that in the judgment of the investigator may interfere with study participation or the ability to follow the intervention protocol.
- •Pregnancy is to be avoided during the study. Women who have not had a hysterectomy or oophorectomy must have a negative urine pregnancy test result at screening. Women of childbearing potential will be allowed to participate if they have undergone tubal ligation, or use one of the following types of contraception: properly used condom or diaphragm, oral contraceptives, hormonal implant, or intrauterine device (IUD). Sexual abstinence may constitute an acceptable birth control method for this study with investigator approval. Women with male partners who have had a successful vasectomy (more than one year of unprotected sexual intercourse without pregnancy) are not required to use additional birth control methods as long as the relationship remains exclusive, and the woman agrees to use an approved contraception method with any other male partner. Questions regarding individual patient contraceptive practices should be directed to the Principal Investigator.
研究组 & 干预措施
1
Intensive Medical Intervention including Low Calorie Liquid Diet, Weight loss medications, Group Behavioral Therapy and a "Tool Box" approach
干预措施: group sessions (Behavioral)
1
Intensive Medical Intervention including Low Calorie Liquid Diet, Weight loss medications, Group Behavioral Therapy and a "Tool Box" approach
干预措施: sibutramine, orlistat, diethylpropion (Drug)
1
Intensive Medical Intervention including Low Calorie Liquid Diet, Weight loss medications, Group Behavioral Therapy and a "Tool Box" approach
干预措施: Low Calorie Diet, Health One (Behavioral)
1
Intensive Medical Intervention including Low Calorie Liquid Diet, Weight loss medications, Group Behavioral Therapy and a "Tool Box" approach
干预措施: Intensive Medical Combination Therapy for Obesity (Other)
2
Access to Weight Loss Informational Website sponsored by the Mayo Clinic
干预措施: Control Condition (Other)
结局指标
主要结局
Percent Change From Baseline Weight
时间窗: Baseline, 2 years
次要结局
- Change in Weight From Baseline in Kilograms (kg)(Baseline, 2 years)
- Change in Blood Pressure(Baseline, 2 years)
- Percent Change in Blood Tests- Low Density Lipoprotein (LDL), High Density Lipoprotein (HDL), Triglycerides and Uric Acid(Baseline, 2 years)
- Change in Fasting Plasma Glucose (FPG) in Milligrams Per Deciliter (mg/dL)(Baseline, 2 years)
- Change in Duke Activity Status Index (DASI) Questionnaire Score(Baseline, 2 years)
研究者
Donna H. Ryan, MD
Professor, Adjunct
Pennington Biomedical Research Center