Strengths-Based Family Psychoeducation for Youth Psychosis

January 2, 2016 updated by: Nao Shiraishi, Nagoya City University

Effectiveness of the Strengths-Based Family Psychoeducation for Youth Psychosis: Randomized Controlled Trial

The onset of Psychosis forces family members to bear a heavy burden of care. The mental well-being of the family is so complicated that it is important to relieve their psychological stresses. Although family psychoeducation has been established as an evidence-based practice especially for schizophrenia, few studies have primarily intended to reduce the distress of the family due to the burden of care. MacFarlane's multifamily psychoeducation is one of the representative models of a group setting, which is based on the behavioral therapeutic approach. In such psychological interventions, it has been emphasized to focus on the strengths that a person originally has for coping with difficulties. The intervention of mainly drawing the strengths from the family might empower them and lighten their psychological burden.

The first 2-5 years from the onset of psychosis is regarded as the critical period to improve the prognosis, so the intervention including more recent-onset psychotic patients might be of use. With regard to a setting of the psychoeducational intervention, a homogeneous group one can make the program better fitted for their problems. The present study aims to examine if the strength-based family psychoeducaiton for youth psychosis in a group setting in addition to the treatment as usual would be more effective for alleviating the psychological distresses of the family than the treatment as usual alone. Moreover, its impact on the family of recent-onset psychosis is explored as the subgroup.

Study Overview

Status

Completed

Detailed Description

Psychosis, principally involving schizophrenia, is a severe mental illness that commonly develops at a young age and often has a chronic course. The onset of Psychosis forces family members to bear a heavy burden of care. It has been documented over and over again that the mental well-being of the family is complicated. More than a dozen per cent of the family have the morbidity corresponding to be depressive and anxiety disorders. It is important to relieve their psychological stresses.

The concept of the burden of care is so broad and complex that its simple definition is a challenging issue. It is usually defined as objective impacts on the household and subjective consequences, which contain physical, economic, emotional and psychological components. The psychological component involves the stigma against psychiatric disorders. The studies of intervention to the family having a psychotic member have been mostly conducted for the primary interest of reducing the rate of relapse and rehospitalization of the psychotic. Their rationale of the intervention is based on the roles of the family that develop the illness and cause a relapse (e.g., etiological relationship or expressed emotion). Although family psychoeducation has been established as an evidence-based practice especially for schizophrenic patients, few studies have primarily intended to reduce the burden of their family.

Among various types of family psychoeducation, the group setting is considered as a better method in terms of the creation of social support networks, limited medical resources and cost-effectiveness. MacFarlane's multifamily psychoeducation is one of the representative models of a group setting, which is composed of joining sessions, an educational workshop and structured problem-solving group sessions. MacFarlane's model is based on the behavioral therapeutic approach that mainly aims at stopping a vicious cycle. The cycle of schizophrenia is peculiarly caused by expressed emotion, which is negative one expressed by the family that lead to a high relapse rate (e.g., hostility or criticism).

In such psychological interventions, it has been emphasized to focus not only on the vicious cycle but also on strengths. The strengths are defined as the power that a person has originally for coping with difficulties. The intervention of mainly drawing out the strengths of the family might empower them to face difficulties voluntarily and lighten their psychological burden. However, to date, the effectiveness of family psychoeducation based on the strengths approach has not been confirmed.

The onset of psychosis is generally at a young age. The first 2-5 years from the onset of psychosis is regarded as the critical period to improve the prognosis, so the intervention including more recent-onset psychotic patients might be of use. Additionally, the family of a young patient has been reported to have strong concerns about returning to school, going to work and getting married. With regard to a setting of the psychoeducational intervention, a homogeneous group one can make the program better fitted for their problems and heighten group cohesiveness.

The present study aims to examine if the strength-based family psychoeducaiton for youth psychosis in a group setting in addition to the treatment as usual would be more effective for alleviating the psychological distresses of the family than the treatment as usual alone. Moreover, its impact on the family of recent-onset psychosis is explored as the subgroup.

Study Type

Interventional

Enrollment (Actual)

74

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Aichi Prefecture
      • Nagoya City, Aichi Prefecture, Japan, 462-0011
        • Kusunokikai Kusunoki Mental Hospital
      • Nagoya City, Aichi Prefecture, Japan, 468-0073
        • Shiseikai Yagoto Hospital
      • Nagoya City, Aichi Prefecture, Japan, 470-3411
        • Kyouseikai Minamichita Hospital
      • Toyota City, Aichi Prefecture, Japan, 470-0344
        • Kenseikai Toyota-nishi Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

20 years to 74 years (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • The patient

    1. whose age is between 15 and 39 years old
    2. who currently takes outpatient treatment
    3. who fulfills the diagnostic criteria of the DSM-IV-TR for schizophrenia, brief psychotic disorder, schizophreniform disorder, schizoaffective disorder or delusional disorder
    4. who is a native speaker of Japanese
  • The family

    1. whose age is between 20 and 74 years old
    2. who is classified as one of the four relationships with the patient; parent, spouse, sibling and someone who has been living together more than 3 months
    3. who is a native speaker of Japanese

Exclusion Criteria:

  • The patient

    1. who fulfills the diagnostic criteria of the DSM-IV-TR for mood disorders with psychotic features, substance-induced psychotic disorder or psychotic disorder due to the general medical condition
    2. who has been diagnosed with mental retardation or cluster B personality disorders by the doctor in charge
  • The family

    1. who has a communication problem for any reason (e.g. psychotic disorders, dementia or cluster B personality disorders)
    2. who is judged not suitable for participating in this study for any reason by the doctor in charge of the patient

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: SUPPORTIVE_CARE
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Strengths-based family psychoeducation
Family psychoeducation in addition to treatment as usual
Family psychoeducation in a group setting is performed every two weeks for eight weeks.
NO_INTERVENTION: Waiting list
Treatment as usual

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from baseline in the total score of trait anxiety of the Japanese version of the STAI at 14 weeks
Time Frame: Baseline, 10 weeks, 14 weeks
The STAI is a self-report questionnaire to measure the intensity of anxiety. It consists of two categories that are state and trait anxiety. Trait anxiety measures relatively stable responses to anxiety-provoking experiences.
Baseline, 10 weeks, 14 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from baseline in the proportion of the Japanese version of the K6 whose total score is less than nine at 14 weeks.
Time Frame: Baseline, 10 weeks, 14 weeks
The K6 is a self-report questionnaire to measure mental well-being. The range of the score is 0 to 24 and a higher score indicates having poor mental health. The cutoff point is nine. Nine and more scores suggest that 50 percent of the subjects might be depressive or anxiety disorder.
Baseline, 10 weeks, 14 weeks

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from baseline in the total score of the Japanese vesion of the Link's stigma scale
Time Frame: Baseline, 10 weeks, 14 weeks
The Link's stigma scale is a self-report questionnaire to measure the intensity of stigma attached to mental disorders. This scale is intended for general citizens, patients and their family.
Baseline, 10 weeks, 14 weeks
Change from baseline in the total score of state anxiety of the Japanese version of the STAI
Time Frame: Baseline, 10 weeks, 14 weeks
State Anxiety measures temporary situational responses to anxiety-provoking experiences.
Baseline, 10 weeks, 14 weeks
Change from baseline in the total score of the short version of the Japanese version of the Zarit Burden Interview (J-ZBI-8).
Time Frame: Baseline, 10 weeks, 14 weeks
The J-ZBI-8 is a self-report questionnaire to measure the intensity of family care burden. The 8-items short version was developed from the Zarit Burden Interview that contains twenty-two items.
Baseline, 10 weeks, 14 weeks
Change from baseline in the total score of the Japanese version of the family Attitude Scale (FAS).
Time Frame: Baseline, 10 weeks, 14 weeks
The FAS is a self-report questionnaire to measure the intensity of expressed emotion (EE). Hostility, high criticism and low warmth on the Camberwell Family Interview that is the gold standard to masure EE are associated with a higher scores of the FAS.
Baseline, 10 weeks, 14 weeks
Change from baseline in the total score of the Japanese version of the K6
Time Frame: Baseline, 10 weeks, 14 weeks
The K6 is a self-report questionnaire to measure mental well-being. The range of the score is 0 to 24 and a higher score indicates having poor mental health.
Baseline, 10 weeks, 14 weeks
Change from baseline in the score of the Japanese version of the Global Assessment of Functioning (GAF)
Time Frame: Baseline, 10 weeks, 14 weeks
The GAF is an analogous scale that evaluates the current objective symptomatic and functional conditions of patients. The range of the score is 0 to 100 and a higher score indicates having better conditions.
Baseline, 10 weeks, 14 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Nao Shiraishi, MD, Department of Psychiatry and Cognitive-Behavioral Medicine, Nagoya City University Graduate School of Medical Sciences

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

July 1, 2012

Primary Completion (ACTUAL)

January 1, 2016

Study Completion (ACTUAL)

January 1, 2016

Study Registration Dates

First Submitted

November 18, 2012

First Submitted That Met QC Criteria

November 18, 2012

First Posted (ESTIMATE)

November 22, 2012

Study Record Updates

Last Update Posted (ESTIMATE)

January 5, 2016

Last Update Submitted That Met QC Criteria

January 2, 2016

Last Verified

January 1, 2016

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • NCU-708
  • No. 29 (OTHER_GRANT: Aichi Health Promotion Foundation)

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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