This study will determine the effectiveness of a group-based behavioral program for weight reduction in overweight and obese schizophrenia patients.

Condition	Intervention
Schizophrenia Obesity	Behavior: Behavioral training  Behavior: Social skills training  Behavior: Behavioral training booster sessions

Further Study Details: 

Primary Outcomes: Weight reduction
Secondary Outcomes: Weight maintenance
Expected Total Enrollment:  300

Researchers have found a link between schizophrenia, high blood pressure, and insulin resistance; this link puts people with schizophrenia at an increased risk for diabetes and obesity. Weight reduction and maintenance is essential for decreasing these risks. Although data indicate that nonpharmacological interventions for weight loss are viable options, studies to determine their effectiveness have not been conducted. This study will determine the effectiveness of behavioral training for reducing weight in schizophrenia patients. This study will also determine the effects of weight reduction on cardiovascular risk factors in this population.

This study comprises two phases. In Phase 1, participants will be randomly assigned to receive either behavioral training or social skills training for 14 weeks. The behavioral training will teach participants ways to control their diet and increase their physical activity. The social skills training will teach participants how to indirectly control their weight by making social contacts and seeking social support. After 14 weeks, participants in the social skills training group and any participants who have not lost a specified amount of weight will complete the study; participants in the behavioral training group who have a 4% or more weight loss will be enrolled in Phase 2, a 24-month program designed to help participants maintain their weight loss. All participants in Phase 2 will continue to receive weekly behavioral training, but they will be randomly assigned to receive either behavioral training alone or behavioral training combined with biweekly booster treatments where participants discuss their response to different diet and exercise regimens and researchers discuss strategies for increasing one''''s success with the regimens. Interviews, self-report scales, and blood tests will be used to assess participants at study entry, after Phase 1, and at the end of the study. Assessments will include quality of life, self esteem, exercise frequency, blood pressure, serum lipids, and blood glucose.

Ages Eligible for Study:  14 Years   -   60 Years,  Genders Eligible for Study:  Both

Criteria

Inclusion Criteria:

• Diagnosis of schizophrenia or schizoaffective disorder
• Body mass index (BMI) greater than 27
• Stable on antipsychotic drug regimen for at least 1 month prior to study entry
• Parent or guardian willing to provide informed consent, if applicable
• Positive and negative syndrome scale score less than 90
• Willing to use acceptable methods of contraception during the study

Exclusion Criteria:

• Medical contraindication for participating in a weight reduction/exercise program
• Mental retardation
• Current enrollment in another weight management program
• Current use of weight reduction medication
• Unstable cardiovascular or thyroid disease
• Active or end-stage renal disease
• Psychiatric hospitalization within 1 month prior to study entry
• Current use of more than one anti-psychotic medication
• Pregnancy or breastfeeding

Please refer to this study by ClinicalTrials.gov identifier  NCT00158366

Pennsylvania
      Western Psychiatric Institute and Clinic of University of Pennsylvania Medical Center, Pittsburgh,  Pennsylvania,  15213,  United States; Recruiting

Study chairs or principal investigators

Jaspreet Brar, MBBS, MPH,  Principal Investigator,  Western Psychiatric Institute and Clinic of University of Pennsylvania Medical Center   
Rohan Ganguli, MD,  Principal Investigator,  Western Psychiatric Institute and Clinic of University of Pennsylvania Medical Center   

Study ID Numbers:  MH66068-01A2
Last Updated:  September 10, 2005
Record first received:  September 7, 2005
ClinicalTrials.gov Identifier:  NCT00158366
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-09-13