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A Large Pragmatic Cluster Randomized Controlled Trial of a Multi-element Psychosocial Intervention for Early Psychosis (GETUP-PIANO)

Primary Purpose

Psychosis

Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Treatment As Usual (TAU)
TAU+CBT for pts+Family Intervention+CM.
Sponsored by
Universita di Verona
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Psychosis focused on measuring First episode psychosis, Early Psychosis, Cognitive Behavioural therapy, Psychosocial Intervention, Assertive Community treatment, Family Intervention, Mental Disorders, Psychotic Disorders, Schizophrenia and Disorders with Psychotic Features, Affective Disorders, Psychotic

Eligibility Criteria

18 Years - 54 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. age 18-54 yrs
  2. residence in the catchment area of participating Community Mental Health Centres
  3. presence of (a) at least 1 of the following symptoms: hallucinations, delusions, qualitative speech disorder, qualitative psychomotor disorder, bizarre or grossly inappropriate behavior, or (b) at least 2 of the following symptoms: loss of interest, initiative and drive, social withdrawal, episodic severe excitement, purposeless destructiveness, overwhelming fear, marked self-neglect
  4. first lifetime contact with participating CMHC, occasioned by symptoms enumerated in 3.
  5. clinical ICD-10 diagnosis of F20-29; F30.2, F31.2, F31.5, F31.6, F32.3, F33.3, F1x.4; F1x.5; F1x.7;F20-F29, as confirmed after 6 months by using the Schedule for Clinical Assessment in Neuropsychiatry (WHO SCAN)

Exclusion Criteria:

  1. prior anti-psychotic medication (> 3 months) provided by any psychiatric or other medical agencies
  2. mental disorders due to a general medical condition

Sites / Locations

  • University of Verona - Section of Psychiatry and Clinical Psychology, Department of Public Health and Community Medicine

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Treatment As Usual (TAU)

TAU+CBT for pts+Family Intervention+CM

Arm Description

Outcomes

Primary Outcome Measures

Relapses
We define relapse as an episode that has resulted in an admission to a psychiatric inpatient unit (number and days of hospitalization) and/or any case noted record of increase in psychotic symptoms' severity during the study period
Positive and negative symptoms
Positive and Negative symptoms will be measured by the positive and negative subscales of the PANSS and by the PSYRATS

Secondary Outcome Measures

Service Satisfaction in patients and relatives
Service satisfaction will be measured by using the Verona Service Satisfaction Scale, versions for patients and relatives
Patient Functioning
Functionig will be assessed by using the Global Assessment of Functioning Scale and the WHO-Disability Assessment Scale
Patient emotional wellbeing
Emotional wellbeing will be measured by using the anxiety and depression items of the PANSS and the Hamilton-D and selected items of the WHO QoL Scale
Service disengagement
Service disengagement and time to service disengagement will be assessed by consulting case records and local databases
Patient Needs for care
Needs for care will be assessed by using the Camberwell Assessment of Need scale
Key relative expressed emotions
Expressed emotions will be measured by using the Level of Expressed Emotion Scale
Key relative burden
Family burden will be measured by using the Involvement Evaluation Questionnaire

Full Information

First Posted
September 14, 2011
Last Updated
January 7, 2013
Sponsor
Universita di Verona
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1. Study Identification

Unique Protocol Identification Number
NCT01436331
Brief Title
A Large Pragmatic Cluster Randomized Controlled Trial of a Multi-element Psychosocial Intervention for Early Psychosis
Acronym
GETUP-PIANO
Official Title
A Pragmatic Cluster Randomized Controlled Trial of a Multi-element Psychosocial Intervention for Early Psychosis in a 10 Million Inhabitant Catchment Area Aimed to Measure the Treatment's Feasibility and Effectiveness: GET UP-PIANO Trial
Study Type
Interventional

2. Study Status

Record Verification Date
January 2013
Overall Recruitment Status
Completed
Study Start Date
April 2010 (undefined)
Primary Completion Date
May 2012 (Actual)
Study Completion Date
May 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universita di Verona

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Multi-element interventions for first-episode psychosis (FEP) are promising but have mostly been conducted on non epidemiologically representative samples in experimental settings, raising the risk thereby of underestimating the complexities involved in treating onset psychosis in "real world" services. The PIANO Trial (Psychosis early Intervention and Assessment of Needs and Outcome) is part of a more broad-based research program (Genetics, Endophenotype and Treatment: Understanding early Psychosis - GET UP) and aims to: 1) test, at 9 months, the effectiveness, as compared to treatment as usual (TAU) of multi-component psychosocial intervention on a large epidemiologically-based cohort of FEP patients and their family members recruited from a 10 million inhabitant catchment area; 2) identify barriers that may hinder its feasibility and patient/family conditions that can render this type of treatment ineffective or inappropriate; 3) identify clinical, psychological, and environmental and service predictors of treatment effectiveness in FEP. Study participants will be recruited from Community Mental Health Centers (CMHCs) operating for the Italian National Health Service and located in several Northern and Central Regions of Italy. The GET UP PIANO Trial has a pragmatic cluster randomized controlled design, which is considered the gold standard approach for trials that evaluate complex interventions implemented at the institutional level, with the aim of improving health. The assignment units (clusters) are the CMHCs, and the units of observation and analysis are the Centers' patients and their family members. Patients in the experimental group will receive TAU plus: (a) Cognitive-Behavioural Therapy (CBT) sessions, (b) psycho-educational sessions for family members, and c) a case manager, to serve as the patient's referent. Patient enrollment will take place over a 1 year interval, after a 3 month-long piloting. The fidelity of the experimental interventions and the characteristics of TAU will be regularly monitored. Several psychopathological, psychological, functioning and service use variables will be assessed at baseline and 9 month follow-up by independent evaluators. Assuming an expected incidence rate of 17/100.000 per year for functional psychoses (as previously estimated in Italy), the investigators expect to recruit about 800 patients, and 600 relatives. Assuming an attrition rate of about 50%, the size of the trial would detect at 9 months a difference in terms of primary outcome from 25% for the TAU arm to 10% for the intervention arm, with a power of 80%.
Detailed Description
BACKGROUND. It has been shown that most clinical and psychosocial deterioration in psychosis occurs within the first 5 years of illness onset, suggesting thereby that this timeframe is a "critical" period for initiating treatment. Research has therefore more recently focused on early detection and intervention for psychosis, showing that the beneficial effects of antipsychotic medication on first-episode psychosis (FEP) are tempered by the fact that, despite initial symptom reduction, functional recovery is typically poor, even when optimal pharmacological treatment is provided. Family members suffer due to the high emotional burden of being caregivers and frequently show signs of psychological distress. Over the last few years, there has been a growing interest in psychosocial intervention as a means of facilitating recovery and reducing long-term disability associated with psychosis. Literature on psychosocial interventions in FEP can be viewed in terms of two broad categories: 1) studies evaluating specific (i.e. single-element) psychosocial interventions (e.g. individual cognitive behavioral therapy), and 2) studies evaluating comprehensive (i.e. multi-element) interventions, which may include early detection strategies, individual, group, and/or family therapy, and case management (in addition to pharmacological treatment). The latter appear very promising and have been found to be associated with symptom reduction/remission, improved quality of life, increased social and cognitive functioning, low inpatient admission rates, improved insight, high degree of satisfaction with treatment, less time spent in hospital, decreased substance abuse, and fewer self- harm episodes. Most multi-element research programs, however, have been conducted on non-epidemiologically representative samples in experimental settings, raising the risk thereby of underestimating the complexities involved in treating FEP in "real world" services. Moreover, these interventions have rarely tested their efficacy against a control group or, if they have done so, they have used historical or prospective comparison groups, or single-group designs, which track the progress of a single group over a given period of time. With respect to practices, over the last 10 years, some countries have implemented specific early psychosis interventions, but even these have not yet become routinely conducted. Few studies have identified barriers that can hinder the feasibility of these interventions or the pinpointing of patient or family conditions that can render this type of ineffective or inappropriate. Hence, efforts to implement these specific multi-element interventions should be accompanied by rigorous scientific methodology, with the aim of better understanding the actual effectiveness of this approach. AIMS. The PIANO Trial (Psychosis early Intervention and Assessment of Needs and Outcome described herein makes up part of the more broad-based research program Genetics Endophenotypes and Treatment: Understanding early Psychosis (GET UP, National Coordinator: Prof. Mirella Ruggeri, Verona), which is financed by the Italian Ministry of Health as part of a Ricerca Sanitaria Finalizzata and is coordinated by the Azienda Ospedaliera Universitaria Integrata in Verona. GET UP Research Programme consists of 4 partner Projects: PIANO (Psychosis: early Intervention and Assessment of Needs and Outcome); TRUMPET (TRaining and Understanding of service Models for Psychosis Early Treatment); GUITAR (Genetic data Utilization and Implementation of Targeted drug Administration in the clinical Routine); and CONTRABASS (COgnitive Neuroendophenotypes for Treatment and RehAbilitation of psychoses: Brain imaging, inflAmmation and StresS). Each of these partner projects pertains to different areas of research, but are linked together in a high degree of harmonization of effort. The Trial described herein - which is the main component of GET UP PIANO, and the main data collection axis for the overall GET UP Research Program - aims to: 1) test, at 9 months, the effectiveness, as compared to treatment as usual (TAU) of multi-component psychosocial intervention on a large epidemiologically-based cohort of FEP patients recruited from a 10 million inhabitant catchment area; 2) verify the clinical routine limits of this approach, i.e. to identify barriers that may hinder its feasibility and patient/family conditions that can render this type of treatment ineffective or inappropriate; 3) identify clinical, psychological, and environmental and service predictors of treatment effectiveness in FEP, as undertaken in an Italian community mental health care framework. Study participants will be recruited from Community Mental Health Centres (CMHCs) operating for the Italian National Health Service and located in several Northern and Central Regions of Italy. Specifically, the Participating Units (PU) will be located in the Veneto Region (subdivided in the Western Veneto and in the Eastern Veneto PU), the Emilia-Romagna Region (subdivided in the Emilia and Romagna PUs) and in the provinces of Florence, Bolzano, and Milano (subdivided in the Milan Niguarda and in the Milan San Paolo PUs), and thus, overall, a 10 million-inhabitant catchment area. DESIGN. The GET UP PIANO Trial has a pragmatic cluster randomized controlled design, which compares the effectiveness of a multi-element psychosocial treatment for FEP patients and their family members, versus the treatment as usual provided by Italian community mental health services. A cluster design was chosen based on feasibility considerations. In fact, a document drafted by members of the MRC Health Services and Public Health Research Board in 2000 indicated cluster randomisation as the gold standard approach for trials that evaluate complex interventions implemented at the institutional level, with the aim of improving health. The assignment units (clusters) will be the catchment area's CMHC, and the units of observation and analysis will be the Centers' patients and their family members. CMHCs enrollment procedure: The PIANO Trial catchment area has 126 CMHCs (9.951.306 inhabitants), all of which have been officially asked to participate in GET UP; 117 have accepted to participate, covering a catchment area of 9.304.093 inhabitants thereby. In an effort to improve the study design's efficiency, before randomization the investigators divided CMHCs into strata, according to three variables: affiliation to the same community psychiatric service, CMHC catchment area size, urban/mixed vs. rural. The socio-economic levels in the trial catchment area were found to be quite homogeneous, and the variable of urban/mixed vs. rural stratification accounted for most of the differences observed. With the exception of staff members in 5 CMHCS (covering a catchment area of 503.000 inhabitants) the mental health staff of the remaining 112 CMHCs had received no prior training in the intervention used in the trial. These first 5 Centers were therefore forced to the intervention arm, and this subgroup will be used as the expected "gold standard" in the analysis to measure the competence of the remaining professionals. Thus, 112 CMHCs (8.801.093 inhabitants) were available for the randomization procedure and were entered in the randomization procedure, with equal numbers being allocated to each arm. Based on administrative data in these Centers, the at-risk population (18-54 years) was estimated to be approximately 50% of the total inhabitants. Assuming an expected incidence rate of 17/100.000 per year for non affective and affective psychoses (as previously estimated in Italy) the investigators can expect to recruit over one year in the catchment area about 800 patients at their first episode of psychosis, and 600 relatives. Assuming an attrition rate of about 50%, the size of the trial would detect at 9 months a difference in terms of primary outcome from 25% for the TAU arm to 10% for the intervention arm, with a power of 80%. Patient- and family member enrollment procedure: Patient enrollment will take place over a 1 year interval, after a 3 month-long piloting. Interventions begin within one month from intake, and, in any event, as soon as each patient is stabilized. Clinical stabilization is defined as a condition allowing the patient to collaborate in at least a brief examination. Patients in the experimental group will receive treatment as usual plus: (a) Cognitive Behavioural Therapy (CBT) sessions, (b) psycho-educational sessions for family members, and c) a Case Manager (CM), to serve as the patient's referent. Treatment as usual conducted in the control arm CMHSs has been characterized in previous studies. The fidelity of the experimental interventions and the characteristics of treatment as usual will be regularly monitored. BASELINE ASSESSMENT. Before entering the study, patients screening positive for psychosis will be asked to provide informed consent to participate. When patients are considered clinically stabilized (after intake), they will be assessed by independent evaluators with a set of standardized instruments which measure: substance abuse (Clinical Drug Use Scale, CDUS), symptoms (Positive and Negative Syndrome Scale, PANSS; Hamilton Rating Scale for Depression, HAMD; Bech-Rafaelsen Mania rating Scale, BRMRS); global functioning (Global Assessment of Functioning, GAF); Subjective appraisal of positive symptoms (Psychotic Symptom Rating Scales, PSYRATS), social disability (Disability Assessment Scale, WHO-DAS), insight (Schedule for Assessment of Insight, SAI-E), needs for care (Camberwell Assessment of Need, CAN-EU), quality of life (WHO-QOL), life events (first 14 years of life, one year prior to the onset of psychosis, period following onset measured with ad hoc schedule for Life Events, CECA-Q), parental bonding (Parental Bonding Instrument,PBI), and expressed emotions (Level of Expressed Emotion Scale, LEE). Participating patients will be asked for consent to involve their family members in the trial, and when given, family members also providing informed consent will be assessed regarding burden of care (Involvement Evaluation Questionnaire, IEQ) and emotional distress (General Health Questionnaire, GHQ); they will also be interviewed with respect to the patient's pre-morbid adjustment (Pre-morbid Adjustment Scale, PAS) and obstetric complications at birth. FOLLOW-UP ASSESSMENT. After 9 months from baseline, patients will be re-assessed for substance abuse, psychotic symptoms (PANSS and PSYRATS) depression (HAMD, BRMS), global functioning (GAF), social disability (WHO DAS), insight (SAI-E), needs for care (CAN), and quality of life (WHO-QoL). Moreover, patients will be evaluated in terms of pharmacological side effects, pattern of clinical course (Life Chart Schedule), and service satisfaction (Verona Service Satisfaction Scale-Patient version,VSSSP ). Family members will be re-assessed with respect to burden of care (IEQ) and emotional distress (GHQ); they will also be assessed for service satisfaction (VSSS-Relative version).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Psychosis
Keywords
First episode psychosis, Early Psychosis, Cognitive Behavioural therapy, Psychosocial Intervention, Assertive Community treatment, Family Intervention, Mental Disorders, Psychotic Disorders, Schizophrenia and Disorders with Psychotic Features, Affective Disorders, Psychotic

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Treatment As Usual (TAU)
Arm Type
Active Comparator
Arm Title
TAU+CBT for pts+Family Intervention+CM
Arm Type
Experimental
Intervention Type
Other
Intervention Name(s)
Treatment As Usual (TAU)
Other Intervention Name(s)
standard treatment, control treatment
Intervention Description
Services participating in the trial are routine public Community Mental Health Centres (CMHCs), which operate within the Italian National Health Service. Multi-disciplinary teams operating these CMHCs provide a wide range of integrated programmes, including inpatient care, day care, rehabilitation, outpatient care, home visits, 24-hour emergency services, and residential facilities. Standard care for FEP patients generally consists of personalized outpatient psychopharmacological treatment, combined with non-specific supportive clinical management at the CMHC level. Family interventions generally consist of non-specific informal support/educational sessions. Both specialized individual psychotherapeutic interventions for patients (included CBT) and specialized psycho-educational or cognitive-oriented family interventions are usually not provided, due to lack of trained professionals.
Intervention Type
Behavioral
Intervention Name(s)
TAU+CBT for pts+Family Intervention+CM.
Other Intervention Name(s)
Multi-element intervention, Family psychoeducation
Intervention Description
The experimental treatment package is administered by the CMHC staff, after training and with ongoing supervision by experts. Cognitive-behavioural therapy (CBT) is based on the model developed by Kuipers in 1998 and Garety in 2008. A total of 20-30 CBT sessions per patient will be delivered, with weekly sessions during months 1-3 and fortnightly over the following 6 months. Family Intervention is based on the model proposed by Leff in 1982 and further developed by Kuipers in 2002. It includes a total of 10-15 sessions with each individual family: 6 in months 1-3, and at least 1 session/month in the 6 months afterwards. Every patient/family will have a dedicated Case Manager, who will coordinate all planned interventions. Specific training programs have been developed, with assessment of the staff competence. Detailed Manuals based on international standards have been developed and will be used. Fidelity will be measured at the end of the trial.
Primary Outcome Measure Information:
Title
Relapses
Description
We define relapse as an episode that has resulted in an admission to a psychiatric inpatient unit (number and days of hospitalization) and/or any case noted record of increase in psychotic symptoms' severity during the study period
Time Frame
9 months
Title
Positive and negative symptoms
Description
Positive and Negative symptoms will be measured by the positive and negative subscales of the PANSS and by the PSYRATS
Time Frame
change from baseline at 9 month follow-up
Secondary Outcome Measure Information:
Title
Service Satisfaction in patients and relatives
Description
Service satisfaction will be measured by using the Verona Service Satisfaction Scale, versions for patients and relatives
Time Frame
9 months
Title
Patient Functioning
Description
Functionig will be assessed by using the Global Assessment of Functioning Scale and the WHO-Disability Assessment Scale
Time Frame
change from baseline at 9 month follow-up
Title
Patient emotional wellbeing
Description
Emotional wellbeing will be measured by using the anxiety and depression items of the PANSS and the Hamilton-D and selected items of the WHO QoL Scale
Time Frame
change from baseline at 9 month follow-up
Title
Service disengagement
Description
Service disengagement and time to service disengagement will be assessed by consulting case records and local databases
Time Frame
9 months
Title
Patient Needs for care
Description
Needs for care will be assessed by using the Camberwell Assessment of Need scale
Time Frame
change from baseline at 9 month follow-up
Title
Key relative expressed emotions
Description
Expressed emotions will be measured by using the Level of Expressed Emotion Scale
Time Frame
change from baseline at 9 month follow-up
Title
Key relative burden
Description
Family burden will be measured by using the Involvement Evaluation Questionnaire
Time Frame
change from baseline at 9 month follow-up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
54 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: age 18-54 yrs residence in the catchment area of participating Community Mental Health Centres presence of (a) at least 1 of the following symptoms: hallucinations, delusions, qualitative speech disorder, qualitative psychomotor disorder, bizarre or grossly inappropriate behavior, or (b) at least 2 of the following symptoms: loss of interest, initiative and drive, social withdrawal, episodic severe excitement, purposeless destructiveness, overwhelming fear, marked self-neglect first lifetime contact with participating CMHC, occasioned by symptoms enumerated in 3. clinical ICD-10 diagnosis of F20-29; F30.2, F31.2, F31.5, F31.6, F32.3, F33.3, F1x.4; F1x.5; F1x.7;F20-F29, as confirmed after 6 months by using the Schedule for Clinical Assessment in Neuropsychiatry (WHO SCAN) Exclusion Criteria: prior anti-psychotic medication (> 3 months) provided by any psychiatric or other medical agencies mental disorders due to a general medical condition
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mirella RUGGERI, M.D.
Organizational Affiliation
Universita' di Verona
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Verona - Section of Psychiatry and Clinical Psychology, Department of Public Health and Community Medicine
City
Verona
ZIP/Postal Code
37134
Country
Italy

12. IPD Sharing Statement

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PubMed Identifier
28302703
Citation
Lasalvia A, Bonetto C, Lenzi J, Rucci P, Iozzino L, Cellini M, Comacchio C, Cristofalo D, D'Agostino A, de Girolamo G, De Santi K, Ghigi D, Leuci E, Miceli M, Meneghelli A, Pileggi F, Scarone S, Santonastaso P, Torresani S, Tosato S, Veronese A, Fioritti A, Ruggeri M; GET UP Group. Predictors and moderators of treatment outcome in patients receiving multi-element psychosocial intervention for early psychosis: results from the GET UP pragmatic cluster randomised controlled trial. Br J Psychiatry. 2017 May;210(5):342-349. doi: 10.1192/bjp.bp.116.190058. Epub 2017 Mar 16.
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PubMed Identifier
22647399
Citation
Ruggeri M, Bonetto C, Lasalvia A, De Girolamo G, Fioritti A, Rucci P, Santonastaso P, Neri G, Pileggi F, Ghigi D, Miceli M, Scarone S, Cocchi A, Torresani S, Faravelli C, Zimmermann C, Meneghelli A, Cremonese C, Scocco P, Leuci E, Mazzi F, Gennarelli M, Brambilla P, Bissoli S, Bertani ME, Tosato S, De Santi K, Poli S, Cristofalo D, Tansella M; GET UP GROUP; Ruggeri M, Mirella ME, Bissoli S, Bonetto C, Cristofalo D, De Santi K, Lasalvia A, Lunardi S, Negretto V, Poli S, Tosato S, Zamboni MG, Ballarin M, De Girolamo G, Fioritti A, Neri G, Pileggi F, Rucci P, Bocchio Chiavetto L, Scasselatti C, Zanardini R, Brambilla P, Bellani M, Bertoldo A, Marinelli V, Negretto V, Perlini C, Rambaldelli G, Lasalvia A, Bertani M, Bissoli S, Lazzarotto L, Bardella S, Gardellin F, Lamonaca D, Lasalvia A, Lunardon M, Magnabosco R, Martucci M, Nicolau S, Nifosi F, Pavanati M, Rossi M, Piazza C, Piccione G, Sala A, Sale A, Stefan B, Zotos S, Balbo M, Boggian I, Ceccato E, Dall'Agnola R, Gardellin F, Girotto 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A Large Pragmatic Cluster Randomized Controlled Trial of a Multi-element Psychosocial Intervention for Early Psychosis

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