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"Stress in At Risk Mental State: Efficacy of Stress Management Cognitive Behavioral Therapy : a Randomized Controlled Trial"

Not Applicable
Conditions
Young Subjects With at Risk Mental States
Interventions
Other: Cognitive behavioral therapy
Other: Supportive therapy
Registration Number
NCT02368353
Lead Sponsor
Centre Hospitalier St Anne
Brief Summary

The first psychotic episodes are preceded by a pauci-symptomatic phase from 2 to 4 years during which the psychotic symptoms are present at a subliminal level in severity or in frequency. The clinical criteria "mental status with risk" (AR) identifies patients among whom 10 in 40 % will make a psychotic transition in the year.

Our hypothesis is that interventions to reduce reactivity to stress are effective in reducing the intensity of psychotic symptoms in subjects with prodromal psychotic symptoms. Our project is to evaluate a therapy for stress management in at risk patients, compared to a conventional monitoring, and implement a longitudinal follow-up concerning the reduction of psychotic symptoms in conjunction with other markers of stress. Nonstigmatizing, these interventions offer an alternative to antipsychotics all the more interesting since they should also reduce the risk of depression and suicide.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
120
Inclusion Criteria
  • Aged 15 to 25 years
  • Help-seekers in one of the specialized clinics for adolescents or young adults 9
  • Meets CAARMS criteria for 'at risk mental state' (ARMS)
Exclusion Criteria
  • situations of emergency.
  • prengnancy, breast-feeding
  • Forced hospitalization or individuals under legal guardianship.
  • schizophrenia (DSMIV-TR criteria)
  • Low IQ (<70) ,
  • Mother tongue and primary educational language other than French
  • Blindness, deafness, muteness, sensorimotor or language deficits
  • any severe medical condition,
  • Daily cannabis use in the last week
  • Current depression (>20 MADRS scale)
  • Substance dependence or abuse (except nicotine) for more than 5 years.
  • Treatments by benzodiazépine (> 10 mg amount diazépam) or stop of less than 5 days
  • Previous treatment by antipsychotics in a superior dose in more than 100 mg equivalent Chlorpromazine if at least a sequence lasted more than 12 weeks
  • Treatment by antipsychotics measures > 100 mg eq. CPZactuel (superior dose in more than 100 mg equivalent Chlorpromazine) so introduced for less than three weeks
  • Antidepressant treatmentsbegun for less three weeks
  • Treatment by corticoids (except local treatment)
  • Exclusion period of another study;
  • The usual contraindications for MRI
  • Absence of social insurance

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Cognitive behavioral therapy groupCognitive behavioral therapyweekly group stress-management CBT (SM-CBT) - 1/week 3 months
Reference groupSupportive therapyweekly supportive therapy - 1/week 3 months
Primary Outcome Measures
NameTimeMethod
The score at month 6 on the "positive" psychotic dimension of the CAARMS (first subscale including delusion, hallucination and disorganized thoughts).Month 6
Secondary Outcome Measures
NameTimeMethod
Performance score on autobiographic memoryMonth 12
Score on CAARMSMonth 12
· Rate of conversion (as defined by CAARMS)Month 12
Score on YMRSMonth 12
Stress marker : genetic variants that modulate stress responseMonth 12
Score on BPRSMonth 12
Score on MADRSMonth 12
Stress marker : saliva cortisol levelMonth 12
Stress marker : telomerase activityMonth 12
Performance score on sense of self tasksMonth 12
Score on SOFASMonth 12
Stress marker : epigenetic markersMonth 12
Stress marker : hippocampal volumeMonth 12

Trial Locations

Locations (1)

Centre Hospitalier Sainte Anne

🇫🇷

Paris, France

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