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Early and Short Psycho-educational Lifestyle Intervention (HYVIE)

Primary Purpose

Schizophrenia

Status
Terminated
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Motivational group
educational group
Sponsored by
Hôpital le Vinatier
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Schizophrenia focused on measuring Schizophrenia, Obesity, Metabolic Syndrome

Eligibility Criteria

18 Years - 45 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Hospitalized patients in one of four adult psychiatric units of eastern pole of the Hospital Vinatier
  • man or woman
  • aged between 18 (major) and 45 years (age limit on inducing a cardiovascular risk)
  • receiving anti-psychotic medication or antiepileptic mood stabilizer introduced during this hospitalization: patients must be treatment-naive or already under psychotropic drug(s) since less than 10 years

Exclusion Criteria:

  • minor
  • aged over 45 years at inclusion
  • pregnancy or breastfeeding
  • patient suffering from a neurodegenerative disease
  • patient suffering from an eating disorder
  • patient with a BMI> 30
  • patient treated for more than 10 years by anti-psychotic medication or antiepileptic mood stabilizer

Sites / Locations

  • Centre Hospitalier Le Vinatier

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Motivational group

educational group

Arm Description

psycho-education program inspired by motivational interviewing and behavioral psychotherapy

exclusively informative psycho-education program

Outcomes

Primary Outcome Measures

Change in body weight (kg)

Secondary Outcome Measures

Changes in waist circumference (cm)
waist circumference measurement during individual interviews standardized assessment (medical or nursing)
Appearance of a SBP (systolic blood pressure) greater than the pathological threshold (> 140 mmHg) or DBP (diastolic blood pressure) above the pathological level (> 90 mmHg)
Appearance of HDL cholesterol below the pathological threshold (<0.40 g/l) and / or LDL cholesterol greater than the pathological threshold (> 2.20 g/l) and / or higher triglyceride pathological level (> 1.5 g/l)
Appearance of a fasting blood glucose higher than pathological threshold defined by ANAES in 1999 (> 1.26 g/l on two samples)
Increased motivation to participate in a non-hospital treatment group on food and cooking
subjective criterion (declarative) rated on a visual scale in individual interviews standardized assessment (medical or nursing)
Increased motivation to participate in a non-hospital treatment group on physical activity or sport
subjective criterion (declarative) rated on a visual scale in individual interviews standardized assessment (medical or nursing)
Improved knowledge of balance and food hygiene
increase of at least 3 points out of 19 in the note obtained during the evaluation done in individual interviews standardized assessment (medical or nursing)

Full Information

First Posted
January 13, 2016
Last Updated
February 7, 2018
Sponsor
Hôpital le Vinatier
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1. Study Identification

Unique Protocol Identification Number
NCT02657941
Brief Title
Early and Short Psycho-educational Lifestyle Intervention
Acronym
HYVIE
Official Title
Early and Short Psycho-educational Lifestyle Intervention to Prevent Weight Gain Induced by Psychotropic Drugs in Adults With Severe Mental Illness: a Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
February 2018
Overall Recruitment Status
Terminated
Why Stopped
inclusion problem
Study Start Date
December 9, 2015 (Actual)
Primary Completion Date
November 14, 2017 (Actual)
Study Completion Date
November 14, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hôpital le Vinatier

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
People with severe mental illness have an increased risk of somatic comorbidities such as metabolic syndrome, obesity, hypertension, dyslipidemia and diabetes mellitus, which induce an increased risk of early mortality, mainly because of cardiovascular diseases. These high cardio-metabolic risks result of several factors such as lack of access to medical care, a poor and unbalanced nutrition, physical inactivity and smoking but they are also exacerbated by antipsychotic medications and anti-epileptic mood stabilizers prescribed to treat their psychiatric disorder. These prevention and awareness interventions in lifestyle are most often implemented in ambulatory stabilized patients. Also weight gain occurs in the early months of treatment. The therapeutic education program evaluated in this study seeks to potentiate the effectiveness of these preventive measures through early awareness in hospitalized patients. Finally, this study aims to compare the efficacy of two early and short programs on health behavior: first a program inspired by motivational interviewing and behavioral psychotherapy and secondly an exclusively educational program (information, formative assessment).
Detailed Description
This both psychoeducational programs have a common objective through different methods to promote early awareness of the lifestyle (physical activity and dietary balance) of hospitalized adult patients who receive a psychotropic medication that may cause increased morbidity cardiovascular mortality through excessive weight gain and development of metabolic syndrome. Both programs have the same number of sessions of the same duration (three weekly sessions of one hour); the same themes are addressed (risk of weight gain and cardiovascular risks induced by treatments, benefits of physical activity and of a balanced diet); only the psycho-educational methods differ. These programs are for patients with serious mental illness (mainly psychotic disorders and mood disorders), hospitalized in one of the four adult psychiatric units of the Eastern Sector of the Vinatier Hospital in Bron, France. Patients are treatment-naive or already under psychotropic drug(s) but a new antipsychotic or mood-stabilizer must have been started during this hospitalization. Patients are included on indication of their referring physician in hospital, as soon as their clinical status is compatible. They are randomized to one of two therapeutic educational groups. The two parallel modules of psycho-education are co-managed by two nurses specialized in psycho-education. The study is based on a module per month for 18 months. Patients included will receive three individual interviews with a nurse or psychiatrist: the first interview before module, the second after module and the third three months after module.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenia
Keywords
Schizophrenia, Obesity, Metabolic Syndrome

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
10 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Motivational group
Arm Type
Experimental
Arm Description
psycho-education program inspired by motivational interviewing and behavioral psychotherapy
Arm Title
educational group
Arm Type
Active Comparator
Arm Description
exclusively informative psycho-education program
Intervention Type
Behavioral
Intervention Name(s)
Motivational group
Intervention Description
Three weekly sessions of one hour, co-managed by two nurses specialized in psycho-education Session 1: General information on the risk of weight gain and the means of prevention, motivational balance on the practice of physical activity, developing a personal goal, information about the sports center Session 2: brainstorming and card game on Food Hygiene Session 3: Find situations at risk of snacking and consider alternative lines
Intervention Type
Behavioral
Intervention Name(s)
educational group
Intervention Description
Three weekly sessions of one hour, co-managed by two nurses specialized in psycho-education Session 1: General information on the risk of weight gain and means of prevention, video on physical activity, discussions with therapists, information about the sports center Session 2: Video on Food Hygiene, discussions with therapists Session 3: Return on basic concepts covered in the first 2 sessions
Primary Outcome Measure Information:
Title
Change in body weight (kg)
Time Frame
Change from baseline after 3 months
Secondary Outcome Measure Information:
Title
Changes in waist circumference (cm)
Description
waist circumference measurement during individual interviews standardized assessment (medical or nursing)
Time Frame
Change from baseline after 3 months
Title
Appearance of a SBP (systolic blood pressure) greater than the pathological threshold (> 140 mmHg) or DBP (diastolic blood pressure) above the pathological level (> 90 mmHg)
Time Frame
Change from baseline after 3 months
Title
Appearance of HDL cholesterol below the pathological threshold (<0.40 g/l) and / or LDL cholesterol greater than the pathological threshold (> 2.20 g/l) and / or higher triglyceride pathological level (> 1.5 g/l)
Time Frame
Change from baseline after 3 months
Title
Appearance of a fasting blood glucose higher than pathological threshold defined by ANAES in 1999 (> 1.26 g/l on two samples)
Time Frame
Change from baseline after 3 months
Title
Increased motivation to participate in a non-hospital treatment group on food and cooking
Description
subjective criterion (declarative) rated on a visual scale in individual interviews standardized assessment (medical or nursing)
Time Frame
Change from baseline after 3 months
Title
Increased motivation to participate in a non-hospital treatment group on physical activity or sport
Description
subjective criterion (declarative) rated on a visual scale in individual interviews standardized assessment (medical or nursing)
Time Frame
Change from baseline after 3 months
Title
Improved knowledge of balance and food hygiene
Description
increase of at least 3 points out of 19 in the note obtained during the evaluation done in individual interviews standardized assessment (medical or nursing)
Time Frame
Change from baseline after 3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Hospitalized patients in one of four adult psychiatric units of eastern pole of the Hospital Vinatier man or woman aged between 18 (major) and 45 years (age limit on inducing a cardiovascular risk) receiving anti-psychotic medication or antiepileptic mood stabilizer introduced during this hospitalization: patients must be treatment-naive or already under psychotropic drug(s) since less than 10 years Exclusion Criteria: minor aged over 45 years at inclusion pregnancy or breastfeeding patient suffering from a neurodegenerative disease patient suffering from an eating disorder patient with a BMI> 30 patient treated for more than 10 years by anti-psychotic medication or antiepileptic mood stabilizer
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
MAGES NICOLAS, PH
Organizational Affiliation
Responsable de service G08 - Villeurbanne et de l'Unité Polaire de Psychoéducation, Pôle Est, Centre Hospitalier Le Vinatier
Official's Role
Principal Investigator
Facility Information:
Facility Name
Centre Hospitalier Le Vinatier
City
Bron Cedex
ZIP/Postal Code
69678
Country
France

12. IPD Sharing Statement

Plan to Share IPD
No

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Early and Short Psycho-educational Lifestyle Intervention

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