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CompletedNCT01075295Updated Jul 25, 2017

Prevention of Weight Gain in Early Psychoses

An interventional study of Behavioural Intervention for the Prevention of Weight Gain and TAU in Schizophreniform Disorder, Bipolar I Disorder and Bipolar II Disorder, sponsored by Centre for Addiction and Mental Health. Completed at 1 site in Canada. Open to participants aged 14 Years to 45 Years. Per ClinicalTrials.gov, last updated 2017-07-25.

Sponsored by Centre for Addiction and Mental Health · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
70
Allocation
Randomized
Ages
14 Years to 45 Years
Sex
All
01

Study summary

The purpose of this study is to determine whether individuals with psychotic spectrum disorders ( Schizophrenia, Schizoaffective disorder,Schizophreniform Disorder, Bipolar Disorder (Type I),Bipolar Disorder (Type II),Major Depressive Disorder With Psychotic Features,Substance-Induced Psychoses,Psychosis Not-Otherwise-Specified (NOS)randomly assigned to a stepped behavioral intervention for the prevention of weight gain will experience less weight gain than individuals who receive usual care. There are several studies that have examined the effect of pharmacological and non-pharmacological behavioural approaches for weight loss in patients with psychosis, however studies examining strategies for prevention of obesity are lacking. This study is an important and novel approach to studying the problem of obesity in those with psychosis.

Read the detailed description

The rates of obesity and related co-morbidities are several-fold higher in patients with psychosis than in the general population. In addition the life expectancy 20% shorter. Several lifestyle and illness-related factors have been implicated for these high rates, including weight gain associated with treatment with novel antipsychotics. The most important cause of death in psychosis patients is coronary heart disease (CHD), of which obesity is a major risk factor. As well, diabetes and its associated complications occur at high rates in persons with psychosis, and diabetes is both related to obesity and is an independent risk factor for CVD and mortality. It therefore seems reasonable to assume that prevention of obesity may lead to a reduced risk for CVD and diabetes. If the proposed intervention proves successful in preventing weight gain and reducing risk for CVD and diabetes, the quality and length of life for persons with psychosis will be vastly improved and medical costs reduced.

Specifically, we hypothesize that : 1a) a smaller proportion of those in the intervention will gain weight (2% or more) as compared to those receiving usual care, 1b) the mean weight gain of those randomized to the intervention will be less than the mean weight gain in those randomized to usual care 2) Increases in Body Mass Index (BMI) and waist circumference (WC) will be smaller in the intervention group as compared to the controls. 3) there will be smaller increases in cholesterol, triglycerides, blood glucose and insulin levels in the intervention group than in the control group. Exploratory analyses of changes in makers for systemic inflammation, and their relationship to weight, and lipid changes, will be conducted to develop novel hypotheses regarding mediators of CVD risk in psychosis.

The study will recruit sixty persons or outpatients with DSM-lV Psychosis with a BMI of \< 30 kg/m², who have been treated for less than 2 years (Early SZ) and meet the other enrollment criteria. They will be randomly assigned in the allocation ratio 1:1 to either get a stepped behavioural intervention for prevention of weight gain (n=30) or treatment as usual (routine care, n=30). This will be a pragmatic clinical trial of 16-week duration.

02

Conditions studied

  • Schizophreniform Disorder
  • Bipolar I Disorder
  • Bipolar II Disorder
  • Major Depressive Disorder
  • Substance-Induced Psychoses
  • Psychosis Not Otherwise Specified
  • Schizophrenia
  • Schizoaffective Disorder

Keywords

  • Schizophreniform Disorder
  • Schizophrenia, Schizoaffective disorder
  • Bipolar I Disorder
  • Bipolar II Disorder
  • Major Depressive Disorder with Psychotic Features,
  • Substance-Induced Psychoses
  • Psychosis Not Otherwise Specified
  • antipsychotic
  • weight gain
  • body mass index
  • BMI
  • waist circumference
  • WC
  • coronary heart disease
  • CHD
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In context

Weight Gain

405 studies on the registry are indexed under Weight Gain; 52 are open to participants now.

This study's enrollment of 70 is below the median of 83 across 324 interventional studies indexed under Weight Gain.

Browse Weight Gain studies →

Lead sponsor

Centre for Addiction and Mental Health is the lead sponsor of 327 studies on the registry; 51 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
14 Years to 45 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Age between 14 and 45 years (inclusive)
  • Male or Female gender
  • DSM-IV-TR diagnosis of Schizophrenia, Schizoaffective disorder,Schizophreniform Disorder, Bipolar Disorder (Type I),Bipolar Disorder (Type II), Major Depressive Disorder With Psychotic Features, Substance-Induced Psychoses, Psychosis Not-Otherwise-Specified (NOS)
  • Outpatient status at the time of randomization
  • Duration of antipsychotic treatment of less than 5 years
  • Ability to provide informed consent
  • Female patients of childbearing potential must be using a medically accepted means of contraception
  • Treatment with olanzapine, clozapine, quetiapine,risperidone or paliperidone for less than 8 weeks duration at enrollment
  • BMI between 18.5 and 30

Exclusion criteria

Exclusion Criteria:

  • Inability to give informed consent
  • Currently enrolled in a weight management program
  • Currently being treated with a medication to reduce weight
  • Patients with unstable or active cardiovascular illnesses (myocardial infarction, congestive heart failure, etc), active or end-stage renal disease, and unstable thyroid disease, etc

Inclusion/exclusion criteria has been intentionally limited in order to maximize the generalizability of the study.

05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
70 participants (actual)

Study arms

  • Experimental
    Lifestyle Intervention

    Behavioral: Behavioural Intervention for the Prevention of Weight Gain

  • Active comparator
    TAU

    Other: TAU

Interventions

  • BehavioralBehavioural Intervention for the Prevention of Weight Gain

    The intervention consists of four steps: * STEP 1 (Watchful Waiting): Measurement of body weight and Waist Circumference at the start (1 visit). Subjects that have a weight gain greater then or equal to 2% of their baseline weight will progress to Step 2 * STEP 2 (Self monitoring): Self-monitoring of daily weight, daily food intake \& physical activity (1 visit) Subjects that have a weight gain greater then or equal to 2% (from STEP 2) will progress to Step 3 * STEP 3 (Nutrition \& Exercise Counseling): Counseling for nutrition and physical activity (4 visits; 2 in-clinic, 2 telephone) Subjects that have a weight gain greater then or equal to 2% (from STEP 3) will progress to Step 4 * STEP 4 (Intensive): Intensive behavioral training geared towards reducing caloric intake (4 in-clinic visits)

  • OtherTAU

    Treatment as provided by individuals' existing healthcare providers

06

What researchers measure

Primary outcomes

  1. Weight

    The proportion with an increase in weight (2% or greater), from baseline to end point.

    Time frame: Measured at week 0, 4, 8 and 16

Secondary outcomes

  1. Laboratory parameters

    * Fasting glucose * Insulin * Lipids

    Time frame: Measured at week 0 and 16

07

Study locations

1 site
  • Centre for Addiction and Mental Health
    Toronto, Ontario M5T 1R8, Canada
08

References and documents

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 25, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT01075295
Lead sponsor
Centre for Addiction and Mental Health
Collaborators
Canadian Institutes of Health Research (CIHR)
Responsible party
Rohan Ganguli (M.D., Centre for Addiction and Mental Health) — Principal investigator
First posted
Feb 25, 2010
Start date
Feb 2010
Primary completion
Dec 2012
Completion
Dec 2012
Last update
Jul 25, 2017

Study contacts

Rohan Ganguli, MD
principal investigator · Centre for Addiction and Mental Health

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jul 2017. You cannot join it, but the record below documents what was studied.

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