Bipolar Disorder, Schizoaffective Disorder, Schizophrenia, Schizophreniform Disorder, Severe Major Depression With Psychotic Features
Conditions
Keywords
antipsychotic, severe mental illness, weight loss
Brief summary
This study is designed to look at the effects of naltrexone on weight loss in individuals treated with antipsychotic medications. Naltrexone is an FDA approved medication for the management of alcohol dependence and drug dependence, but has not been fully evaluated for its effect on weight loss in individuals with severe mental illness (i.e. schizophrenia, schizoaffective disorder, bipolar disorder etc.) The purpose of this study is to find out how effective two different doses of oral naltrexone is on reducing body weight when compared to placebo (an inactive substance or sugar pill).
Detailed description
Persons with severe mental illness (SMI) die, on average, 25 years earlier than the general population1. Most of this early mortality can be attributed to cardiovascular disease (CVD) and diabetes mellitus (DM), which are directly related to obesity. Obesity is a leading cause of preventable death in the United States, second only to smoking. The physical health of patients has become a major focus of schizophrenia care, as recent decades have seen immense gains in symptom control and community integration. There is an urgent need for the development of interventions that address the obesity crisis in schizophrenia. Patients treated with antipsychotic medications have been shown to have a preference for diets high in fat and sugar. Patients with schizophrenia typically seek behaviors that increase dopamine mediated reward in the brain such as smoking and substance use, both of which occur more often in this group than the general population. The system might require intact dopamine and opioid function. Naltrexone is an oral agent that competitively antagonizes all known opioid receptors in the brain. Human studies with naltrexone were completed in individuals with different illnesses, including schizophrenia, and have been shown to be a safe and easy agent to use. It is shown to decrease craving in alcoholics and is approved by the FDA for the treatment of alcohol dependence. Naltrexone is reported to decrease craving for other substances of abuse, like nicotine. Furthermore, it has been shown to prevent secondary weight gain due to cessation of cigarette smoking at low (25mg and 50 mg), but not higher doses. Naltrexone has been tested in human feeding studies, and has been shown to reduce both the quantity of food eaten and the choice of palatable foods. Subjects will be randomized to either 25, 50 or 0mg of Naltrexone and will take the study medication daily for 52 weeks. Subjects will be seen weekly for the first 4 weeks of the study, thereafter they will be seen on a bi-weekly (every other week) basis to be assessed (i.e. weight, side effect check, paper questionnaires) throughout the remaining 48 weeks of treatment. The purpose of this study is to determine the efficacy of two doses of naltrexone (25mg & 50mg) versus placebo for weight and health risk reduction in 144 obese individuals with severe mental illness treated with an antipsychotic medication.
Interventions
25 or 50mg (randomized) oral capsule taken once daily for 52 weeks to establish optimal dose for weight loss over the course of the study.
Sponsors
Study design
Eligibility
Inclusion criteria
* Age 18 to 75 * Meet Diagnostic & Statistical Manual - 4 (DSM-IV) criteria for schizophrenia, schizoaffective disorder, bipolar disorder, major depression, or another psychotic disorder based on Structured Clinical Interview for the DSM-IV (SCID) interview * Body Mass Index (BMI) of 28 and over * On a stable dose of antipsychotic medication; i.e. at least one month with no dose change, and three months from an antipsychotic switch * Deemed to be symptomatically stable by the clinical staff in the last two months * Over 7% total body weight increase on antipsychotics for subjects within first year of illness
Exclusion criteria
* Meet criteria for current opiate abuse or dependence (confirmed by positive urine drug screen for opiates or, if suspected by study doctor via patient history and or suspicion of occult opiate use, a naloxone challenge will be performed.) * Current history of dementia, mental retardation * Not capable of giving informed consent for participation in the study * Women who are pregnant or breast-feeding * Physical conditions affecting body weight (e.g. Cushing's disease, polycystic ovary syndrome) Diabetes Mellitus (defined as prescribed an anti-diabetic medication for diabetes or a hemoglobin A1c level \> 7 confirmed by primary care physician at screening) * Severe liver dysfunction, (serum aminotransferases greater than three times normal), acute infectious hepatitis, liver failure.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change in Weight From Baseline | Baseline and 52 weeks | Weight (kilograms; kg) will be measured at each assessment and change in weight will be determined at study endpoint. |
| Percent of Subjects Who Lost More Than 5% of Body Weight From Baseline | 52 weeks | Body Mass Index will be calculated at each assessment and change over time will be assessed at endpoint. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Changes in Insulin From Baseline | Baseline and 52 weeks | Insulin will be collected over the course of participation and changes will be evaluated at study endpoint. |
| Changes in Total Cholesterol From Baseline | Baseline and 52 weeks | Total Cholesterol will be collected over the course of participation and changes will be evaluated at study endpoint. |
| Changes in Fasting Glucose From Baseline | Baseline and 52 weeks | Fasting glucose will be collected over the course of participation and changes will be evaluated at study endpoint. |
| Changes in LDL From Baseline | Baseline and 52 weeks | Low-density lipoprotein (HDL) will be collected over the course of participation and changes will be evaluated at study endpoint. |
| Changes in HDL From Baseline | Baseline and 52 weeks | High-density lipoprotein (HDL) will be collected over the course of participation and changes will be evaluated at study endpoint. |
| Changes in Glycosylated Hemoglobin (HbA1c) From Baseline | Baseline and 52 weeks | Glycosylated hemoglobin (HbA1c) will be collected over the course of participation and changes will be evaluated at study endpoint. |
Countries
United States
Participant flow
Participants by arm
| Arm | Count |
|---|---|
| Placebo Oral placebo capsule taken once daily for 52 weeks
Placebo | 51 |
| Naltrexone 25mg Oral Naltrexone 25mg capsule taken once daily for 52 weeks
Naltrexone: 25 or 50mg (randomized) oral capsule taken once daily for 52 weeks to establish optimal dose for weight loss over the course of the study. | 47 |
| Naltrexone 50mg Oral Naltrexone 50mg capsule taken once daily for 52 weeks
Naltrexone: 25 or 50mg (randomized) oral capsule taken once daily for 52 weeks to establish optimal dose for weight loss over the course of the study. | 46 |
| Total | 144 |
Withdrawals & dropouts
| Period | Reason | FG000 | FG001 | FG002 |
|---|---|---|---|---|
| Overall Study | Adverse Event | 1 | 5 | 4 |
| Overall Study | Death | 0 | 1 | 0 |
| Overall Study | Lost to Follow-up | 11 | 18 | 13 |
| Overall Study | Non-compliance | 1 | 0 | 1 |
| Overall Study | Physician Decision | 0 | 1 | 2 |
| Overall Study | Pregnancy | 2 | 0 | 0 |
| Overall Study | Protocol Violation | 1 | 0 | 0 |
| Overall Study | Unrelated Hospitalization | 2 | 0 | 1 |
| Overall Study | Withdrawal by Subject | 1 | 2 | 0 |
Baseline characteristics
| Characteristic | Placebo | Naltrexone 25mg | Naltrexone 50mg | Total |
|---|---|---|---|---|
| Age, Continuous | 42.8 years STANDARD_DEVIATION 12.8 | 45.0 years STANDARD_DEVIATION 11.5 | 43.0 years STANDARD_DEVIATION 14.2 | 43.6 years STANDARD_DEVIATION 12.8 |
| Body Mass Index (BMI) | 39.1 weight in kg/ height m^2 STANDARD_DEVIATION 7.3 | 37.1 weight in kg/ height m^2 STANDARD_DEVIATION 5.7 | 38.9 weight in kg/ height m^2 STANDARD_DEVIATION 11.4 | 38.4 weight in kg/ height m^2 STANDARD_DEVIATION 8.4 |
| Race/Ethnicity, Customized African American | 24 Participants | 28 Participants | 16 Participants | 68 Participants |
| Race/Ethnicity, Customized Other | 9 Participants | 3 Participants | 3 Participants | 15 Participants |
| Race/Ethnicity, Customized White/Caucasian | 18 Participants | 16 Participants | 27 Participants | 61 Participants |
| Region of Enrollment United States | 51 participants | 47 participants | 46 participants | 144 participants |
| Sex: Female, Male Female | 30 Participants | 22 Participants | 25 Participants | 77 Participants |
| Sex: Female, Male Male | 21 Participants | 25 Participants | 21 Participants | 67 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk | EG002 affected / at risk |
|---|---|---|---|
| deaths Total, all-cause mortality | 0 / 51 | 1 / 47 | 0 / 46 |
| other Total, other adverse events | 35 / 51 | 33 / 47 | 35 / 46 |
| serious Total, serious adverse events | 0 / 51 | 1 / 47 | 0 / 46 |
Outcome results
Change in Weight From Baseline
Weight (kilograms; kg) will be measured at each assessment and change in weight will be determined at study endpoint.
Time frame: Baseline and 52 weeks
Population: Analysis population consists of participants who were randomized, received at least 1 dose of the trial compound (naltrexone or placebo), and had at least 1 assessment after baseline.
| Arm | Measure | Value (LEAST_SQUARES_MEAN) | Dispersion |
|---|---|---|---|
| Placebo | Change in Weight From Baseline | -0.16 kg | Standard Error 1.78 |
| Naltrexone 25mg | Change in Weight From Baseline | 0.69 kg | Standard Error 2.22 |
| Naltrexone 50mg | Change in Weight From Baseline | -0.95 kg | Standard Error 2.06 |
Percent of Subjects Who Lost More Than 5% of Body Weight From Baseline
Body Mass Index will be calculated at each assessment and change over time will be assessed at endpoint.
Time frame: 52 weeks
Population: Analysis population consists of participants who were randomized, received at least 1 dose of the trial compound (naltrexone or placebo), and had at least 1 assessment after baseline.
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Placebo | Percent of Subjects Who Lost More Than 5% of Body Weight From Baseline | 10 Participants |
| Naltrexone 25mg | Percent of Subjects Who Lost More Than 5% of Body Weight From Baseline | 4 Participants |
| Naltrexone 50mg | Percent of Subjects Who Lost More Than 5% of Body Weight From Baseline | 9 Participants |
Changes in Fasting Glucose From Baseline
Fasting glucose will be collected over the course of participation and changes will be evaluated at study endpoint.
Time frame: Baseline and 52 weeks
Population: Analysis population consists of participants who were randomized, received at least 1 dose of the trial compound (naltrexone or placebo), and had at least 1 assessment after baseline.
| Arm | Measure | Value (LEAST_SQUARES_MEAN) | Dispersion |
|---|---|---|---|
| Placebo | Changes in Fasting Glucose From Baseline | 8.2 mg/dL | Standard Error 2.6 |
| Naltrexone 25mg | Changes in Fasting Glucose From Baseline | 4.6 mg/dL | Standard Error 3.2 |
| Naltrexone 50mg | Changes in Fasting Glucose From Baseline | -0.4 mg/dL | Standard Error 2.9 |
Changes in Glycosylated Hemoglobin (HbA1c) From Baseline
Glycosylated hemoglobin (HbA1c) will be collected over the course of participation and changes will be evaluated at study endpoint.
Time frame: Baseline and 52 weeks
Population: Analysis population consists of participants who were randomized, received at least 1 dose of the trial compound (naltrexone or placebo), and had at least 1 assessment after baseline.
| Arm | Measure | Value (LEAST_SQUARES_MEAN) | Dispersion |
|---|---|---|---|
| Placebo | Changes in Glycosylated Hemoglobin (HbA1c) From Baseline | -0.007 mg/dL | Standard Error 0.11 |
| Naltrexone 25mg | Changes in Glycosylated Hemoglobin (HbA1c) From Baseline | -0.061 mg/dL | Standard Error 0.15 |
| Naltrexone 50mg | Changes in Glycosylated Hemoglobin (HbA1c) From Baseline | 0.060 mg/dL | Standard Error 0.39 |
Changes in HDL From Baseline
High-density lipoprotein (HDL) will be collected over the course of participation and changes will be evaluated at study endpoint.
Time frame: Baseline and 52 weeks
Population: Analysis population consists of participants who were randomized, received at least 1 dose of the trial compound (naltrexone or placebo), and had at least 1 assessment after baseline.
| Arm | Measure | Value (LEAST_SQUARES_MEAN) | Dispersion |
|---|---|---|---|
| Placebo | Changes in HDL From Baseline | 0.04 mg/dL | Standard Error 1.73 |
| Naltrexone 25mg | Changes in HDL From Baseline | 0.79 mg/dL | Standard Error 2.19 |
| Naltrexone 50mg | Changes in HDL From Baseline | 0.36 mg/dL | Standard Error 1.93 |
Changes in Insulin From Baseline
Insulin will be collected over the course of participation and changes will be evaluated at study endpoint.
Time frame: Baseline and 52 weeks
Population: Analysis population consists of participants who were randomized, received at least 1 dose of the trial compound (naltrexone or placebo), and had at least 1 assessment after baseline.
| Arm | Measure | Value (LEAST_SQUARES_MEAN) | Dispersion |
|---|---|---|---|
| Placebo | Changes in Insulin From Baseline | 6.45 mg/dL | Standard Error 4.89 |
| Naltrexone 25mg | Changes in Insulin From Baseline | 0.45 mg/dL | Standard Error 6.23 |
| Naltrexone 50mg | Changes in Insulin From Baseline | 2.16 mg/dL | Standard Error 5.55 |
Changes in LDL From Baseline
Low-density lipoprotein (HDL) will be collected over the course of participation and changes will be evaluated at study endpoint.
Time frame: Baseline and 52 weeks
Population: Analysis population consists of participants who were randomized, received at least 1 dose of the trial compound (naltrexone or placebo), and had at least 1 assessment after baseline.
| Arm | Measure | Value (LEAST_SQUARES_MEAN) | Dispersion |
|---|---|---|---|
| Placebo | Changes in LDL From Baseline | -10.87 mg/dL | Standard Error 4.47 |
| Naltrexone 25mg | Changes in LDL From Baseline | 1.14 mg/dL | Standard Error 5.46 |
| Naltrexone 50mg | Changes in LDL From Baseline | -4.40 mg/dL | Standard Error 4.91 |
Changes in Total Cholesterol From Baseline
Total Cholesterol will be collected over the course of participation and changes will be evaluated at study endpoint.
Time frame: Baseline and 52 weeks
Population: Analysis population consists of participants who were randomized, received at least 1 dose of the trial compound (naltrexone or placebo), and had at least 1 assessment after baseline.
| Arm | Measure | Value (LEAST_SQUARES_MEAN) | Dispersion |
|---|---|---|---|
| Placebo | Changes in Total Cholesterol From Baseline | -1.16 mg/dL | Standard Error 5.12 |
| Naltrexone 25mg | Changes in Total Cholesterol From Baseline | 1.52 mg/dL | Standard Error 6.41 |
| Naltrexone 50mg | Changes in Total Cholesterol From Baseline | -3.02 mg/dL | Standard Error 5.72 |