Lifestyle Modification and Liraglutide

Completed · Phase 4 · Has a placebo group

Conditions studied: Obesity

In brief

This is a 52 week, single center, open-labeled, randomized controlled trial. A total of 150 subjects with obesity, who are free of types 1 and 2 diabetes, as well as contraindications to weight loss, will be randomly assigned to one of three treatment groups: 1) lifestyle counseling, as currently recommended by the Centers for Medicare and Medicaid Services (CMS) (i.e., CMS-Alone); 2) CMS lifestyle counseling plus liraglutide (i.e., CMS-Liraglutide); or 3) CMS-Liraglutide plus a portion-controlled diet (i.e., Multi-Component Intervention). Subjects in all three groups will have 14 brief (15 minute) lifestyle counseling visits the first 24 weeks, followed by monthly visits in weeks 25-52. This is the schedule and duration of counseling visits recommended by CMS. Counseling sessions will be delivered by a physician, nurse practitioner or registered dietitian (RD) working in consultation with the former providers. Subjects in all three groups also will have brief physician visits at weeks 1, 4, 8, 16, 24, 36, and 52 (total of 7 visits). These visits are needed for subjects in both liraglutide groups to monitor their response to the medication. These visits are included for subjects in CMS-Alone to match the intensity of medical care provided the two other groups. The primary outcome is % reduction in initial body weight, as measured from randomization to week 52. Secondary outcomes include the proportion of participants who at week 52 lose \>5%, \>10%, and \>15% of initial weight, as well as % reduction in weight at week 24 and the proportion of participants who meet the three categorical weight losses at this time. The secondary efficacy measures include changes (from randomization to week 52) in cardiovascular disease (CVD) risk factors, glycemic control, mood, quality of life, eating behavior, appetite, sleep, and satisfaction with weight loss. Safety endpoints will include physical examination, adverse events (AEs), standard laboratory tests, and mental health assessed by the Columbia Suicidality Severity Rating Scale (C-SSRS) and Patient Health Questionnaire (PHQ-9). Statistical Analysis. Using a sample size equation for longitudinal clustered samples, a randomization sample of 50 subjects in CMS-Alone, 50 in CMS-Liraglutide, and 50 in the Multi-Component Intervention provides \>80% power to detect the two primary contrasts to be statistically significant. This estimate allows for 20% attrition during the 52-week trial, resulting in approximately 40 treatment completers per group. The ITT longitudinal statistical design will further improve power by allowing the inclusion of available data for non-completers and the adjustment of possible variance reducing baseline covariates.

Key facts

Study ID: NCT02911818
Run by: University of Pennsylvania
People needed: 150
Starts: 2016-09-01
Expected to finish: 2018-12-01
Last updated by the study team: 2019-05-07

Who can join

Age: 21 and older, up to 70. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Participants must have a BMI ≥ 30 and ≤ 55 kg/m²
Age ≥ 21 years and ≤ 70 years
Eligible female patients will be:
non-pregnant, evidenced by a negative urine dipstick pregnancy test
non-lactating
surgically sterile or postmenopausal, or they will agree to continue to use an accepted method of birth control during the study
Ability to provide informed consent before any trial-related activities
Participants must:
have a primary care provider (PCP) who is responsible for providing routine care
have a reliable telephone service with which to communicate with study staff
understand and be willing to comply with all study-related procedures and agree to participate in the study by giving written informed consent
plan to remain in the Philadelphia area for the next 18 months

You may not qualify if…

Pregnant or nursing, or plans to become pregnant in the next 18 months, or not using adequate contraceptive measures
Personal or family history of medullary thyroid cancer or multiple endocrine neoplasia syndrome type 2
Uncontrolled hypertension (systolic blood pressure ≥ 160 mm Hg or diastolic blood pressure ≥ 100 mm Hg)
Type 1 diabetes
Type 2 diabetes
A fasting glucose ≥ 126 mg/dl (on second assessment after first elevated value)
Recent history of cardiovascular disease (e.g., myocardial infarction or stroke within the past 6 months), congestive heart failure, or heart block greater than first degree
Clinically significant hepatic or renal disease
Thyroid disease, not controlled
History of malignancy (except for non-melanoma skin cancer) in past 5 years
Current major depressive episode, active suicidal ideation, or history of suicide attempts
Psychiatric hospitalization within the past 6 months
Self-reported alcohol or substance abuse within the past 12 months, including at-risk drinking (current consumption of ≥ 14 alcoholic drinks per week)
Use in past 3 months of medications known to induce significant weight loss (i.e., prescription weight loss medications) or weight gain (e.g., chronic use of oral steroids, second generation antipsychotics)
Loss of ≥ 10 lb of body weight within the past 3 months
History of (or plans for) bariatric surgery
Inability to walk 5 blocks comfortably or engage in some other form of aerobic activity (e.g., swimming)
Known or suspected allergy to trial medication(s), excipients, or related products
Hypersensitivity to liraglutide or any product components
The receipt of any investigational drug within 6 months prior to this trial
Previous participation in this trial (e.g., randomized and failed to participate)
History of pancreatitis
Subjects will be included/excluded according to the latest updated US PI.
12-Week Extension Trial:
Inclusion Criteria

Where it is running

University of Pennsylvania Center for Weight and Eating Disorders — Philadelphia, Pennsylvania, United States

Full record on ClinicalTrials.gov

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