Efficacy of Lifestyle Interventions and Metformin for the Treatment of Antipsychotic-Induced Weight Gain
Information source: Central South University
Information obtained from ClinicalTrials.gov on August 03, 2007
Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Weight Gain
Intervention: metformin (Drug); lifestyle intervention (Behavioral)
Phase: Phase 4
Status: Completed
Sponsored by: Central South University Official(s) and/or principal investigator(s):
Jingping Zhao, MD, Study Director, Affiliation: Central South University
Summary
Lifestyle intervention and certain medications have been shown to be effective for antipsychotic-induced weight gain, but no controlled studies have compared psychological and pharmacological therapies. We conducted a randomized, placebo-controlled study to test the efficacy of lifestyle intervention and metformin alone and in combination for antipsychotic-induced weight gain.
Clinical Details
Official title:
Efficacy of Lifestyle Interventions and Metformin for the Treatment of Antipsychotic-Induced Weight Gain: a Randomized Double-Blind Placebo- Controlled Comparison
Study design: Interventional, Treatment, Randomized, Double-Blind, Placebo Control, Factorial Assignment, Efficacy Study
Primary outcome: body weight, body mass index, waist circumference, fasting glucose, fasting insulin, insulin resistance index
Detailed description:
The study was designed as a double-blind randomized controlled trial, with research assessors and patients intended to be blind to the intervention status. The staff members performing the assessment were not involved in implementing any aspect of the intervention. 128 patients were randomized to one of four 12-week individual treatments: metformin (750mg/day), placebo, lifestyle intervention plus metformin (750mg/day) or lifestyle intervention plus placebo. Medications were provided in double-blind fashion. The assessments include body weight, body mass index, waist circumference, fasting glucose, fasting insulin and insulin resistance index.
Eligibility
Minimum age: 18 Years.
Maximum age: 45 Years.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- All participants met the Diagnostic and Statistical Manual of Mental Disorder-Fourth Edition (DSM-Ⅳ) criteria for schizophrenia27.
- Participants were required to get weight gain more than 10% of their predrug body weight during less than 12 months of treatment with a targeted antipsychotic agent- clozapine, olanzapine, risperidone or sulpiride.
- The duration of illness for all participants was less than 12 months.
- Participants could be taking only one antipsychotic, whose dose had not changed by changed by more than 25% over the past 3 months.
- All patients were stable outpatient.
- The total score of Positive and Negative Syndrome Scale (PANSS) for all patients could be ≤60.
- All participants were ensured that they could be carefully taken care of by one of their parents or guardians during the trial.
Exclusion Criteria:
- Participants were excluded from the study if they had evidence of liver or renal diseases, pregnant or lactating women, cardiovascular diseases, hypertension or diabetes mellitus, specific systemic diseases, or conditions that limited their ability to perform the lifestyle modifications, such as arthritis, pulmonary diseases, neurological or dietary restrictions.
Locations and Contacts
Institute of Mental Health of The Second Xiangya Hospital, Central South University, Changsha, Hunan 410011, China
Additional Information
Starting date:
October 2004
Ending date: December 2006
Last updated: March 22, 2007
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