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Efficiency Assessment of BREFORM. A Multicentric Stepped-wedge Randomized Control Trial.

Efficiency Assessment of a Mental Health Professionals' Training Course for a Short Psychoeducational Program (BREF) for Families and Caregivers of Patients With Schizophrenia or First Psychotic Episode.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05036590
Acronym
BREFORM
Enrollment
206
Registered
2021-09-05
Start date
2022-04-05
Completion date
2026-12-31
Last updated
2026-06-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Schizophrenia

Brief summary

In psychiatry, caregiver burden is associated with excess physical and psychological morbidity in relatives of patients with schizophrenic disorders Single or multi-family psychoeducation for caregivers of patients with schizophrenic disorders or first episode psychosis has a direct benefit on the health of the caregiver and an indirect benefit on the health of the ill family member. It is associated with a reduction in the rate of relapse and re-hospitalization and with better compliance with treatment. For single-family psychoeducation, the number of caregivers to be treated to avoid re-hospitalization of the sick family member is 3. For caregivers, psychoeducation is accompanied by an improvement in knowledge of the disorders and coping strategies. Therefore, international recommendations recommend that psychoeducation for caregivers be systematic, early, and integrated into routine care. Currently, the organization of the French care system does not allow these recommendations to be met. In order to increase the use of psychoeducation in France, early interventions for caregivers must be offered systematically. The effectiveness of early psychoeducation for caregivers needs to be evaluated; only three randomized controlled trials are available in the literature and none have been conducted in France.

Detailed description

The BREFORM project proposes to train health professionals in an early psychoeducation program, the BREF program, in order to implement it in their structure, and to evaluate its impact on the burden of caregivers of users living with a first psychotic episode or a schizophrenic disorder. Regarding caregivers' outcomes: outcome measures will be assessed at baseline (visit 1, V1), 6 weeks (Visit 2, V2), 6 months (Visit 3, V3), 12 months (Visit 4, V4) after baseline in the active group and in the treatment as usual group Regarding patients' outcomes: outcome measures will be assessed at baseline and 12 months after baseline in the active group and in the treatment as usual group Regarding mental health professionals' outcomes: outcome measures will be assessed before, after and 16 months after the training course Regarding the psychiatric departments' outcomes: outcome measures will be assessed at baseline and 36 months after baseline

Interventions

OTHERcontrol group

The control group consisted of caregivers included during the control period, before the intervention was deployed, i.e., before the BREF program was implemented by the centers.

OTHERIntervention group

The intervention group consists of caregivers included during the intervention period. Caregivers in the intervention group will benefit from the BREF program.

Sponsors

Hôpital le Vinatier
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Intervention model description

Multicentric Stepped-wedge Randomized Control Trial

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* people over 18yo * first-degree relatives (parents, siblings, children) or spouse of the patient * primary caregiver of a patient with schizophrenic disorders or first psychotic episode (DSM5) * consenting to participate to the study

Exclusion criteria

* mental disorder on Axis I * having already benefited from a family intervention such as psychoeducation * caring for several people with severe psychiatric disorders * receiving income for the caring activities * being legally responsible of the patient * having difficulty understanding fluent French * illiterate

Design outcomes

Primary

MeasureTime frameDescription
Changes in the severity of caregiver burden between V1 and V4 by the Zarit Burden Inventory scale (ZBI)one yearThe ZBI consists of 22 items rated on a 5-point Likert scale that ranges from 0 (never) to 4 (nearly always) with the sum of scores ranging between 0-88. Higher scores indicate greater burden. A score of 17 or more was considered high burden.

Secondary

MeasureTime frameDescription
Changes in caregiver burden severity at V1,V2 and V3 by the Zarit Burden Inventory (ZBI) scale8 monthsThe ZBI consists of 22 items rated on a 5-point Likert scale that ranges from 0 (never) to 4 (nearly always) with the sum of scores ranging between 0-88. Higher scores indicate greater burden. A score of 17 or more was considered high burden.
Evolution of the caregivers' perceived-stress between V1, V2, V3, V4 by the Perceived Stress Scale-14 (PSS-14)one yearTotal score of the PSS can be obtained by summing the 14 items' scores . The total score ranges from 0 to a maximum of 56, a higher score indicating a higher level of perceived stress.
Evolution of the caregivers' mood between V1, V2, V3, V4 by the Center for Epidemiologic Studies-Depression Scale (CES-D)one yearThe CES-D consists of 20 items in a self-report format measuring depressive symptoms experienced in the past week on a 4-point Likert scale ranging from 0 (rarely or none of the time) to 3 (most or all of the time). Depression Severity: 0-4 none, 5-9 mild, 10-14 moderate, 15-19 moderately severe, 20-27 severe. ... PHQ-9 score ≥10 had a sensitivity of 88% and a specificity of 88% for major depression.
Evolution of the caregivers' family functioning between V1, V2, V3, V4one yearAssessed by the Family Assessment Device scale (FAD)
Evolution of the caregivers' quality of life between V1, V2, V3, V4one yearAssessed by the Schizophrenia CareGiver Quality of Life scale (S-CGQoL)
Evolution of the caregivers' sense of competence between V1, V2, V3, V4one yearassessed by the Sense of Competence Questionnaire scale (SCQ)
Evolution of the caregivers' number of consultations with the general practitioner (GP)12 months period before baseline assessment versus 12 months period after baseline assessmentChange in number of consultations with the general practitioner (GP) n the 12 months prior to inclusion compared to the 12 months following inclusion
Evolution of the caregivers' number of days off work12 months period before baseline assessment vs. 12 months period after baseline assessmentChange in number the caregivers' number of days off work in the 12 months prior to inclusion compared to the 12 months following inclusion
Evolution of the caregivers' number of days on long-term leave or disability12 months period before baseline assessment vs. 12 months period after baseline assessmentChange in the number of long-term leaves of absence or disability related to the caregiver situation in the 12 months prior to inclusion compared to the 12 months following inclusion
Evolution of the caregivers' number of work days12 monthsChange in the number of work days related to the caregiver situation in the 12 months prior to inclusion compared to the 12 months following inclusion
Evolution of the caregivers' willingness to pay someone to replace them in their caring activities during one hour12 monthsChange in caregivers' willingness to pay someone to replace them in their caregiving activities for one hour in the 12 months prior to inclusion versus 12 months after inclusion.
Evolution of the caregivers' number of suicide attempts assessed by the Columbia Suicide Severity Rating Scale (C-SSRS)12 months period before baseline assessment vs. 12 months period after baseline assessmentThe Columbia Suicide Severity Rating Scale (C-SSRS) is a measure used to identify and assess individuals at risk for suicide. Questions are phrased for use in an interview format, but can be completed as a self-report measure if necessary. The score is created at each assessment for each patient and is used for determining treatment emergence. Suicidal Ideation Score: The maximum suicidal ideation category (1-5 on the C- SSRS) present at the assessment. Assign a score of 0 if no ideation is present.
caregivers' satisfaction12 monthsquestionnaire
Evolution of the caregivers' living status (shared or non-shared household) between V1, V2, V3, V412 monthsquestionnaire
Evolution of the caregivers' informal caregiving activities between V1, V2, V3, V412 monthsquestionnaire
Evolution of the caregivers' number of hours spent providing informal caregiving between V1, V2, V3, V412 monthsquestionnaire
Evolution of the patients' psychotic symptoms severity between baseline and 12 months after baseline assessed by the Positive And Negative Syndrome Scale (PANSS)12 months period before baseline assessment vs. 12 months period after baseline assessmentPANSS items are rated on a 7-point scale (1=absent, 2=minimal, 3=mild, 4=moderate, 5=moderate severe, 6=severe, and 7=extreme); because the absence of symptoms is equal to 1 point, the lowest possible total score on both PANSS scales is 7.
Evolution of the patients' functioning level between baseline and 12 months after baselineBaseline assessment and 12 months after baseline assessmentAssessed by the Global Assessment of Functionning scale (GAF)
Evolution of the patients' functioning level assessed by the Personal and social Performance scale (PSP)Baseline assessment and 12 months after baseline assessmentThe patient's degree of severity in the four domains is to be rated on a six-point scale from absent (which means no problems on this dimension) over mild, manifest, marked, severe to very severe difficulties in the given area. Out of the ratings on the four subdimensions, one total score on a 100-point scale can be created. A variation of eight points is already to be classified as a clinically relevant difference. The items "self-care" and "disturbing and aggressive behavior" are of greater concern for patients with acute
Evolution of the patients' quality of life between baseline and 12 months after baselineBaseline assessment and 12 months after baseline assessmentAssessed by the Schizophrenia-quality of Life scale (S-QoL)
Evolution of the patients' clinical severity between baseline and 12 months after baselineBaseline assessment and 12 months after baseline assessmentAssessed by the Clinical Global Impression (CGI)
Evolution of the patients' depressive symptoms between baseline and 12 months after baselineBaseline assessment and 12 months after baseline assessmentAssessed by the Calgary Depression Scale for Schizophrenia scale (CDSS)
Evolution of the patients' relapse risk factors between baseline and 12 months after baselineBaseline assessment and 12 months after baseline assessmentComposite score assessed by the Medication Adherence Rating Scale (MARS) and Birchwood Scale (Birchwood), substance use disorders (declarative questionnaire)
Evolution of the patients' number of suicide attempts12 months period before baseline assessment vs. 12 months period after baseline assessmentAssessed by the Columbia Suicide Severity Rating Scale " (C-SSRS)
Evolution of the patients' suicide risk levelBaseline assessment and 12 months after baseline assessmentAssessed by the Columbia Suicide Severity Rating Scale " (C-SSRS)
Evolution of the patients' aggressive behaviors12 months period before baseline assessment vs. 12 months period after baseline assessmentquestionnaire
Evolution of the patients' number of hospitalization in psychiatry12 months period before baseline assessment vs. 12 months period after baseline assessmentnumber of hospitalization in psychiatry
Evolution of the mental health professionals' beliefs and knowledge about psychoeducation to caregiversAssessed before, after and 16 months after the training coursequestionnaire
Evolution of the mental health professionals' sense of competence about psychoeducation to caregiversAssessed before, after and 16 months after the training courseSelf-assessment before, after and 16 months after the training course
Evolution of the mental health professionals' satisfaction of the training courseAssessed after and 16 months after the training coursequestionnaire
Evolution of the mental health professionals' satisfaction of the BREF programAssessed 16 months after the training coursequestionnaire
Evolution of the psychiatric department organization regarding caregivers interventionsAssessed at baseline and 36 months after baselinequestionnaire
Sustainability of the BREF program in each psychiatric departmentAssessed 36 months after baselineQuestion the referent person at the center to know if the program is still used 3 years after its implementation QUESTION THE REFERENT PERSON AT THE CENTER TO KNOW IF THE PROGRAM IS STILL USED 3 YEARS AFTER ITS IMPLEMENTATION Question the referent perso of the center to know if the program is still used 3 years after its implementation

Countries

France

Contacts

CONTACTRomain REY, MD, PhD
romain.rey@ch-le-vinatier.fr+33437915495
CONTACTAnne-Lise BOHEC, PhD
Anne-lise.BOHEC@ch-le-vinatier.fr+33437915495
PRINCIPAL_INVESTIGATORRomain REY, MD, PhD

CH LE VINATIER

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 13, 2026