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Study on Psychoeducation Enhancing Results of Adherence in Schizophrenia (SPERA-S)

Primary Purpose

Patient Non-Compliance, Schizophrenia and Related Disorders

Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Falloon et al. Psychoeducation Program
Generic Treatment
Sponsored by
University of Cagliari
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Patient Non-Compliance focused on measuring Adherence, Psychoeducation, Pharmacotherapy, Schizophrenia, Family support

Eligibility Criteria

18 Years - 55 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • diagnosis of psychosis in the spectrum of schizophrenia (ICD-10: F20 to F29); -age from 18 to 55;
  • being in care for 2 years or more.

Exclusion Criteria:

  • mental retardation, or any severe cognitive impairment;
  • psychosis due to substance abuse or to a medical condition;
  • affective psychosis;
  • comorbid substance dependence;
  • patient does not understand Italian language;
  • pharmacotherapy with depot.

Sites / Locations

  • Università Degli Studi Di Urbino "Carlo Bo"
  • Università Degli Studi Di Bari
  • Fatebenefratelli Irccs
  • Azienda Universitaria Ospedaliera Cagliari
  • Università Degli Studi Di Cagliari
  • Ausl 3 Centro Molise Di Campobasso
  • Università Degli Studi Di Catania
  • Azienda Ospedaliera Universitaria Policlinico Martino Di Messina

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Falloon et al. Psychoeducation Program

Generic Treatment

Arm Description

The intervention aims to improve communication and problem-solving abilities in patients and their families by sessions focused on: assessment of the individual's and the family's strengths, weaknesses, and goals; education about schizophrenia and treatment; communication skills training; problem-solving

The comparator is a treatment with generic informative prospect on the disorders and with the same frequencies as the Intervention. Treatment sessions are provided on a weekly basis for 6 months (1 hour for each session) (groups of about 8-9 persons - patients and caregivers).

Outcomes

Primary Outcome Measures

Adherence
Adherence will be checked with a triple method of assessment: patient's self-report, patient's replies to a four-query interview, and assessment of blood levels of the prescribed drug.

Secondary Outcome Measures

Psychotic symptoms
The occurrence of psychotic symptoms, according to the Brief psychiatric Rating Scale (BPRS) and the Positive and Negative Syndrome Scale (PANSS)
General level of psychopathology
The general level of psychopathology will be measured according to the Health of the Nation rating scale (HoNOS)
Changes in the social functioning
Social functioning will be measured according to Personal and Social Performance scale (PSP). Quality of life will be measured as well, using the WHO-Quality of Life-Short version (WHOQOL-Bref).
Readmission
An episode of readmission is any admission to a psychiatric service for the necessity of controlling symptoms, behavior or therapy. Admission to the hospital for reason of somatic illness will be not considered an episode of readmission.

Full Information

First Posted
August 20, 2011
Last Updated
September 6, 2017
Sponsor
University of Cagliari
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1. Study Identification

Unique Protocol Identification Number
NCT01433094
Brief Title
Study on Psychoeducation Enhancing Results of Adherence in Schizophrenia
Acronym
SPERA-S
Official Title
Study on Psychoeducation Enhancing Results of Adherence in Schizophrenia
Study Type
Interventional

2. Study Status

Record Verification Date
September 2017
Overall Recruitment Status
Completed
Study Start Date
September 2012 (Actual)
Primary Completion Date
May 2016 (Actual)
Study Completion Date
December 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Cagliari

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Background: Psychosis in the spectrum of schizophrenia (PSS) are severe mental disorders, with a high impact on disability and participation. Poor adherence to pharmacotherapy negatively impacts on the course and outcome of PSS. Non-adherence in these patients is 41 to 50%, and it is predictive of a higher risk of relapse and readmission up to 5-time higher than in adherent patients. Falloon et al. developed a Psychoeducation Program (FPP) aimed at improving communication and problem-solving abilities in patients and their families. Past studies reported a statistically significant reduction of the risk of relapse in patients receiving the FPP, but did not take into account effects on adherence. Objectives: To evaluate changes in adherence to pharmacotherapy in a sample of patients diagnosed with PSS (ICD-10: F20 to F29), by comparing a group exposed to the FPP with another group exposed to a treatment with generic informative prospects on the disorders provided with same attendance frequency as the FPP (Generic Treatment - GT). Methods: 340 patients with PSS, from 10 participating units distributed in the territory of the Italian National Health System, will be enrolled, with allocation 1:1. The sample will be randomized into an exposed group (to FPP) and an unexposed group. Adherence will be assessed on a three-monthly basis with blood levels of the primary prescribed drug by High Pressure Liquid Chromatography, with a self-report, the Medication Adherence Questionnaire, and concurrently with the administration of a 4-item interview, based on a modified version of the Adherence Interview. Survival analyses will be performed using Kaplan-Meier method, followed by Log-rank test, defining as terminal events both the start of non-adherence and/or the first relapse or readmission episode. Intention-to-treat will be applied in considering the primary and secondary outcomes. Multiple imputations will be applied to integrate missing data. Expected results: Median prevalence of non-adherence to pharmacotherapy in patients already in contact with a psychiatric service is 47%; effect size of psychosocial treatment on various outcomes, including relapse, readmission and adherence to drug is 0.48 of the standard deviation (SD), with 95% C.I.=0.10 to 0.85. The intervention is expected to produce a change in the prevalence of non-adherence to drug in the exposed group with an effect size of 0.45 SD.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Patient Non-Compliance, Schizophrenia and Related Disorders
Keywords
Adherence, Psychoeducation, Pharmacotherapy, Schizophrenia, Family support

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
112 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Falloon et al. Psychoeducation Program
Arm Type
Experimental
Arm Description
The intervention aims to improve communication and problem-solving abilities in patients and their families by sessions focused on: assessment of the individual's and the family's strengths, weaknesses, and goals; education about schizophrenia and treatment; communication skills training; problem-solving
Arm Title
Generic Treatment
Arm Type
Active Comparator
Arm Description
The comparator is a treatment with generic informative prospect on the disorders and with the same frequencies as the Intervention. Treatment sessions are provided on a weekly basis for 6 months (1 hour for each session) (groups of about 8-9 persons - patients and caregivers).
Intervention Type
Behavioral
Intervention Name(s)
Falloon et al. Psychoeducation Program
Other Intervention Name(s)
Family psychoeducation
Intervention Description
The intervention aims to improve communication and problem-solving abilities in patients and their families by sessions focused on: assessment of the individual's and the family's strengths, weaknesses, and goals; education about schizophrenia and treatment; communication skills training; problem-solving training; and special problems (Falloon et al. 1985). Treatment sessions are provided on a weekly basis for months (1 hour for each session) (groups of about 8-9 persons - patients and caregivers).
Intervention Type
Behavioral
Intervention Name(s)
Generic Treatment
Intervention Description
The comparator is a treatment with generic informative prospect on the disorders and with the same frequencies as the Intervention. Treatment sessions are provided on a weekly basis for 6 months (1 hour for each session) (groups of about 8-9 persons - patients and caregivers).
Primary Outcome Measure Information:
Title
Adherence
Description
Adherence will be checked with a triple method of assessment: patient's self-report, patient's replies to a four-query interview, and assessment of blood levels of the prescribed drug.
Time Frame
Change from baseline in adherence to treatment at 6 months
Secondary Outcome Measure Information:
Title
Psychotic symptoms
Description
The occurrence of psychotic symptoms, according to the Brief psychiatric Rating Scale (BPRS) and the Positive and Negative Syndrome Scale (PANSS)
Time Frame
Changes from baseline in levels of psychotic symptoms at 6 months, with effects maintained at12 months and 18 months
Title
General level of psychopathology
Description
The general level of psychopathology will be measured according to the Health of the Nation rating scale (HoNOS)
Time Frame
Changes from baseline in levels of general psychopathology at 6 months, with effects maintained at 12 and 18 months
Title
Changes in the social functioning
Description
Social functioning will be measured according to Personal and Social Performance scale (PSP). Quality of life will be measured as well, using the WHO-Quality of Life-Short version (WHOQOL-Bref).
Time Frame
Changes from baseline in social functioning at 6 months, maintained at 12 and 18 months
Title
Readmission
Description
An episode of readmission is any admission to a psychiatric service for the necessity of controlling symptoms, behavior or therapy. Admission to the hospital for reason of somatic illness will be not considered an episode of readmission.
Time Frame
Occurrence of episodes of readmission over 27 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: diagnosis of psychosis in the spectrum of schizophrenia (ICD-10: F20 to F29); -age from 18 to 55; being in care for 2 years or more. Exclusion Criteria: mental retardation, or any severe cognitive impairment; psychosis due to substance abuse or to a medical condition; affective psychosis; comorbid substance dependence; patient does not understand Italian language; pharmacotherapy with depot.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
donatella rita petretto, PhD eq
Organizational Affiliation
Department of Psychology, State University of Cagliari
Official's Role
Principal Investigator
Facility Information:
Facility Name
Università Degli Studi Di Urbino "Carlo Bo"
City
Urbino
State/Province
Urbino/Pesaro
Country
Italy
Facility Name
Università Degli Studi Di Bari
City
Bari
Country
Italy
Facility Name
Fatebenefratelli Irccs
City
Brescia
Country
Italy
Facility Name
Azienda Universitaria Ospedaliera Cagliari
City
Cagliari
Country
Italy
Facility Name
Università Degli Studi Di Cagliari
City
Cagliari
Country
Italy
Facility Name
Ausl 3 Centro Molise Di Campobasso
City
Campobasso
Country
Italy
Facility Name
Università Degli Studi Di Catania
City
Catania
Country
Italy
Facility Name
Azienda Ospedaliera Universitaria Policlinico Martino Di Messina
City
Messina
Country
Italy

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
2864032
Citation
Falloon IR, Boyd JL, McGill CW, Williamson M, Razani J, Moss HB, Gilderman AM, Simpson GM. Family management in the prevention of morbidity of schizophrenia. Clinical outcome of a two-year longitudinal study. Arch Gen Psychiatry. 1985 Sep;42(9):887-96. doi: 10.1001/archpsyc.1985.01790320059008.
Results Reference
background
PubMed Identifier
24099414
Citation
Petretto DR, Preti A, Zuddas C, Veltro F, Rocchi MB, Sisti D, Martinelli V, Carta MG, Masala C; SPERA-S group. Study on psychoeducation enhancing results of adherence in patients with schizophrenia (SPERA-S): study protocol for a randomized controlled trial. Trials. 2013 Oct 7;14:323. doi: 10.1186/1745-6215-14-323.
Results Reference
background
Citation
Petretto DR, Lussu C, Zuddas C, Pistis I, Piras P, Preti A, et al. Meta-Review of Systematic and Meta-Analytic Reviews on Family Psychoeducation for Schizophrenia. Austin J Clin Neurol 2017; 4(2): 1107.
Results Reference
background

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Study on Psychoeducation Enhancing Results of Adherence in Schizophrenia

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