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Efficacy of ISST in Schizophrenia

Efficacy of Integrated Social Cognitive and Behavioral Skills Therapy (ISST) in Improving Functional Outcome in Schizophrenia

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02678858
Enrollment
177
Registered
2016-02-10
Start date
2016-03-31
Completion date
2022-03-31
Last updated
2022-08-04

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

Conditions

Schizophrenia

Keywords

social cognition, social skills, cognitive remediation, functional outcome, treatment adherence

Brief summary

The ISST study investigates whether integrated social cognitive remediation and social behavioral skills therapy is more efficacious in improving functional outcome and treatment adherence than an active control treatment comprising drill-and-practice oriented neurocognitive remediation.

Detailed description

Deficits in social functioning are a defining, very burdening feature of schizophrenia precluding patients from participating in a satisfying life. Traditional drug and psychosocial therapy and available specific treatment strategies that directly target single key determinants of functional outcome like neurocognition, social cognition, and social behavioral skills have produced only moderate effects leaving an urgent need for further optimization. The present trial aims to more efficaciously improve functional outcome by integrating social behavioral and social cognitive treatment strategies. Six months of Integrated Social Cognitive and Behavioral Skills Therapy (ISST) will be compared with Neurocognitive Remediation Therapy (NCRT) as active control condition in a randomized multicenter clinical trial using a two group pre-post design with 2x90 patients in the remitted early phase of schizophrenia. Beyond all-cause-discontinuation as common primary outcome of all clinical trials of the ESPRIT-consortium, measures of functional outcome and subjective quality of life, patient experience as well as neurocognitive, social-cognitive and social behavioral measures will be assessed at baseline (V0), after completion of treatment (V6), and after 6 months follow-up (V12). ISST is expected to reduce the one-year discontinuation rate by 20% compared with NCRT, and to be superior in functional outcome measures by an effect size of at least d=0.42.

Interventions

BEHAVIORALIntegrated Social Cognitive and Behavioral Skills Therapy

The Integrated Social Cognitive and Behavioral Skills Therapy (ISST) is a newly developed treatment program. It is based on the Training of Affect Recognition (Wölwer et al. 2005) and common social skills trainings, which are combined in an integrated rather than a sequenced manner. ISST uses both repeated practice and strategy-based training, and consists of 12 individual sessions, 5 group sessions and 1 individual final session over a period of 6 months.

BEHAVIORALNeurocognitive Remediation Therapy

The Neurocognitive Remediation Program (NCRT) is based on a neurocognitive training already used as active control condition in our earlier studies (Wölwer et al. 2005, Klingberg et al. 2011). The present version of NCRT is matched in dose, mode and scheme of application to the ISST, but differs from the ISST regarding targeted cognitive domains and preferred training strategy (predominantly drill and practice based). The NCRT provides the same amount of group interaction and companionship as well as the same amount of guided community activity as in the ISST, but is structured in such a way that interactional behavior is secondary (e.g. by competition-like tasks rather than cooperative tasks). Thus therapeutic attention and commitment are held constant across study conditions.

Sponsors

University Hospital, Bonn
CollaboratorOTHER
University Hospital of Cologne
CollaboratorOTHER
University Hospital Tuebingen
CollaboratorOTHER
Zentralinstitut für Seelische Gesundheit Mannheim
CollaboratorOTHER
University of Cologne
CollaboratorOTHER
Rheinhessen-Fachklinik Alzey
CollaboratorOTHER
Vivantes Klinikum am Urban
CollaboratorUNKNOWN
Heinrich-Heine University, Duesseldorf
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Written informed consent * DSM-IV-TR diagnosis of schizophrenia (295.10-30, 295.90) * PANSS at baseline: total score ≤ 75 * Proficiency in German language.

Exclusion criteria

* Lack of accountability * Positive urine drug-screening for illicit drugs at screening (except cannabinoids and benzodiazepines) * Serious suicidal risk at screening visit * Other relevant axis 1-diagnoses according to diagnostic interview (MINI); * Other relevant neurological or somatic disorders * Verbal IQ\<80 (MWT-B)

Design outcomes

Primary

MeasureTime frameDescription
All Cause Discontinuation6 months, 12 monthsAll Cause Discontinuation is defined as 1) not keeping appointments to treatment or diagnostic sessions as scheduled for more than 6 weeks and/or (2) not being traceable despite extensive efforts by the intervention team to reengage the patient throughout the entire intended treatment period and/or (3) withdrawal of consent by the patient (4) rater induced discontinuation of the study treatment (eg. for safety criteria) (5) not taking psychotropic drugs as prescribed for more than 14 consecutive days and/or (6) relevant worsening of symptoms.

Secondary

MeasureTime frameDescription
Treatment Adherence 26 months, 12 monthsDAI-10 (Drug Attitude Scale, Goodstadt et al. 1978)
Treatment Adherence 36 months, 12 monthsPATHEV (Psychotherapy Attitude Scale, Schulte 2005)
Psychosocial Functioning 16 months, 12 monthsFROGS (Functional Remission of General Schizophrenia, Lorca et al. 2009)
Psychosocial Functioning 26 months, 12 monthsUPSA-Brief (University of California Performance Based Skills Assessment, Mausbach et al. 2007)
WHOQUOL-Bref (Quality of Life)6 months, 12 monthsWHOQUOL-BREF (World Health Organization Quality of Life, WHO 1996)
Neurocognitive Performance (verbal memory)6 months, 12 monthsVLMT (verbal learning and memory test, Helmstaedter, Lendt & Lux 2001
Neurocognitive Performance (working memory)6 months, 12 monthsDSF, DSB (digit sequencing forward/backward, Wechsler 1981)
Neurocognitive Performance (processing speed 1)6 months, 12 monthsDSST (digit symbol substitution test, Wechsler 1981)
Treatment Adherence 16 months, 12 monthsSES (Service Engagement Scale, Tait, Birchwood & Trower 2002)
Socialcognitive Performance (affect recognition)6 months, 12 monthsPFA (Picture of Facial Affect Test, Ekman & Friesen 1976)
Socialcognitive Performance (theory of mind)6 months, 12 monthsMASC (Movie for the Assessment of Social Cognition, Dziobek et al. 2006)
Psychopathology/Symptoms 16 months, 12 monthsPANSS (Positive and Negative Syndrome Scale, Kay, Fiszbein & Opler 1987)
Psychopathology/Symptoms 26 months, 12 monthsCDSS (Calgary Depression Rating Scale for Schizophrenia, Addington, Addington & Maticka-Tyndale 1993)
Psychopathology/Symptoms 36 months, 12 monthsBSI (Brief Symptom Inventory, Derogatis & Melisaratos 1983)
SuicidalityAssessed every 4-6 weeks from date of randomization until 1 year or until discontinuation (whatever came first)Incidence of suicide/suicide attempt or severe suicidal crisis (CDSS Item 8 ≥ 2)
Severe symptom worseningAssessed every 4-6 weeks from date of randomization until 1 year or until discontinuation (whatever came first)CGI (Clinical Global Impression Scale Item 2 ≥ 6)
Neurocognitive Performance (processing speed 2)6 months, 12 monthsTMT-A, -B (Trail-Making-Test, Reitan 1956)

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 17, 2026