Sequential Treatment Approaches for Treatment-Resistant Schizophrenia (STATRS)
Sequential Treatment Approaches for Treatment-Resistant Schizophrenia (STATRS): A Randomized Controlled Trial of Pharmacological Optimization and Neuromodulation in Chinese Patients
The goal of this study is to optimize treatment strategies for Chinese patients with treatment-resistant schizophrenia (TRS). It will compare two types of treatment:
- Drug therapy with clozapine alone or in combination with other medications.
- Neuromodulation therapy, modified electroconvulsive therapy (MECT) or magnetic seizure therapy (MST).
The study aims to determine which approach provides better symptom improvement, fewer cognitive side effects, and greater overall safety. The results may provide important clinical evidence to guide future treatment decisions for patients with TRS.
Visão geral do estudo
Status
Status
Condições
Condições
Intervenção / Tratamento
Intervenção / Tratamento
Descrição detalhada
This is a sequential, assessor-blinded randomized controlled trial in Chinese patients with treatment-resistant schizophrenia (TRS). The study consists of two treatment components.
First, clozapine-naive TRS participants will enter an 8-week pharmacological optimization phase and be assigned to one of three treatment groups: clozapine monotherapy, clozapine plus amisulpride, or clozapine plus aripiprazole.
Second, eligible participants will enter a 4-week assessor-blinded neuromodulation phase comparing modified electroconvulsive therapy (MECT) and magnetic seizure therapy (MST). Participants for this phase are either (1) patients who have previously received clozapine and are hospitalized due to symptom exacerbation, or (2) participants who completed the pharmacological optimization phase and showed inadequate response, defined as less than 25% reduction in PANSS total score at Week 8.
The study is expected to provide evidence on the effectiveness, cognitive safety, and overall tolerability of these treatments for TRS. The project has important clinical significance.
Tipo de estudo
Tipo de estudo
Inscrição (Estimado)
Inscrição
Estágio
Estágio
- Fase 3
Contactos e Locais
Contato de estudo
Contato de estudo
- Nome: DengTang Liu, MD, PhD
- Número de telefone: +86-18017311138
- E-mail: erliu110@126.com
Locais de estudo
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Shanghai Municipality
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Shanghai, Shanghai Municipality, China, 200030
- Recrutamento
- Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine
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Contato:
- DengTang Liu, MD, PhD
- Número de telefone: +862164387250-73775
- E-mail: erliu110@126.com
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Critérios de participação
Critérios de elegibilidade
Critérios de elegibilidade
Idades elegíveis para estudo
Aceita Voluntários Saudáveis
Gêneros Elegíveis para o Estudo
Descrição
Inclusion Criteria:
General inclusion criteria applicable to all participants:
- Aged 18 to 55 years at the time of informed consent.
- Participants must meet DSM-5 diagnostic criteria for schizophrenia.
- Meet TRRIP-based criteria for treatment-resistant schizophrenia, defined as inadequate response to at least two different antipsychotic treatment trials, each administered at an adequate dose equivalent to ≥600 mg/day chlorpromazine for a minimum duration of 6 weeks. Have moderate or greater functional impairment, operationalized as a Personal and Social Performance Scale (PSP) score ≤70. Treatment adherence will be evaluated based on available medical records, prescription history and caregiver report.
Eligibility for the pharmacological optimization phase:
• Participants eligible for the pharmacological optimization phase must meet the general TRS criteria above and must be clozapine-naive.
Eligibility for the neuromodulation phase:
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Participants eligible for the neuromodulation phase must meet the TRS criteria described above.
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Participants may enter the neuromodulation phase through either of the following pathways:
- Participants who have previously received clozapine treatment and are hospitalized due to symptom exacerbation or clinical worsening.
- Clozapine-naive TRS participants who complete the pharmacological optimization phase and show inadequate response, defined as less than 25% reduction in PANSS total score at Week 8.
Exclusion Criteria:
- Organic brain disease or neurological disorder that may account for psychotic symptoms, including epilepsy where clinically relevant.
- Current psychoactive substance dependence or substance-related disorder.
- Intellectual disability or Mental retardation.
- Pregnancy, breastfeeding, or planning pregnancy during the study period.
- Severe physical illness or medical contraindication to study medication, MECT, MST.
- Extreme agitation, stupor, active suicidal risk, severe non-cooperation, or high-risk conditions.
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Tratamento
- Alocação: Randomizado
- Modelo Intervencional: Atribuição sequencial
- Mascaramento: Solteiro
Número de braços
Armas e Intervenções
Grupo de Participantes / BraçoGrupo de Participantes / Braço |
Intervenção / TratamentoIntervenção / Tratamento |
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Comparador Ativo: [Phase 1] Clozapine Monotherapy
Phase 1 of the trial is an 8-week randomized controlled trial(RCT); patients will be randomly assigned to one of three treatment arms with different oral antipsychotics, one is Clozapine Monotherapy. Non-responders in phase 1 will switch to phase 2. |
Initial dose: 25-50 mg/day orally. Clozapine will be individually titrated over 8 weeks, with a usual target dose of 300-450 mg/day and a target steady-state trough plasma concentration of ≥350 ng/mL. Plasma clozapine concentration will be assessed at Week 4. If the concentration is <350 ng/mL, the dose will be further increased as clinically tolerated. A dose of ≥300 mg/day is not required if the target plasma concentration is achieved at a lower dose. Participants who cannot reach either 300 mg/day or the target plasma concentration because of intolerance may remain on their maximum tolerated dose below 300 mg/day.
Outros nomes:
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Experimental: [Phase 1] Clozapine + Aripiprazole
Phase 1 of the trial is a 8-week randomized controlled trial(RCT); patients will be randomly assigned to one of three treatment arms with different oral antipsychotics, one of which is 'Clozapine + Aripiprazole'. Non-responders in phase 1 will switch to phase 2. |
Initial dose: 25-50 mg/day orally. Clozapine will be individually titrated over 8 weeks, with a usual target dose of 300-450 mg/day and a target steady-state trough plasma concentration of ≥350 ng/mL. Plasma clozapine concentration will be assessed at Week 4. If the concentration is <350 ng/mL, the dose will be further increased as clinically tolerated. A dose of ≥300 mg/day is not required if the target plasma concentration is achieved at a lower dose. Participants who cannot reach either 300 mg/day or the target plasma concentration because of intolerance may remain on their maximum tolerated dose below 300 mg/day.
Outros nomes:
Initial dose: 5-10 mg/day. Aripiprazole recommended dosage:10-15 mg/day. dosage form:po.duration:8 weeks
Outros nomes:
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Experimental: [Phase 1] Clozapine + Amisulpride
Phase 1 of the trial is a 8-week randomized controlled trial(RCT); patients will be randomly assigned to one of three treatment arms with different oral antipsychotics, one of which is 'Clozapine + Amisulpride'. Non-responders in phase 1 will switch to phase 2. |
Initial dose: 25-50 mg/day orally. Clozapine will be individually titrated over 8 weeks, with a usual target dose of 300-450 mg/day and a target steady-state trough plasma concentration of ≥350 ng/mL. Plasma clozapine concentration will be assessed at Week 4. If the concentration is <350 ng/mL, the dose will be further increased as clinically tolerated. A dose of ≥300 mg/day is not required if the target plasma concentration is achieved at a lower dose. Participants who cannot reach either 300 mg/day or the target plasma concentration because of intolerance may remain on their maximum tolerated dose below 300 mg/day.
Outros nomes:
Initial dose: 200-400 mg/day. Amisulpride recommended dosage: 400-800 mg/day. dosage form:po.duration:8 weeks
Outros nomes:
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Comparador Ativo: [Phase 2] Modified Electroconvulsive Therapy (MECT)
CRS participants will receive modified electroconvulsive therapy while maintaining stable pharmacological treatment. The treatment course consists of 3 times per week for the first two weeks, followed by 2 times per week for the next two weeks, totaling 10 times per month, which is the same number of treatment sessions as the MST group. |
MECT will be administered using a Thymatron System IV device. The electrical charge will be determined according to the participant's age and body weight, with treatment parameters adjusted according to the study protocol and clinical response. Participants will continue the pharmacotherapy regimen received before Phase 2. Medication doses will remain stable whenever clinically feasible; changes will be permitted only when clinically necessary for safety or tolerability and will be documented.
Outros nomes:
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Experimental: [Phase 2] Magnetic Seizure Therapy (MST)
CRS participants will receive magnetic seizure therapy while maintaining stable pharmacological treatment. The treatment course consists of 3 times per week for the first two weeks, followed by 2 times per week for the next two weeks, totaling 10 times per month, which is the same number of treatment sessions as the MECT group. |
MST will be administered using a MagPro X100 magnetic stimulator equipped with the MagOption MST module. The stimulation frequency will be set at 100 Hz and output intensity at 100% of device output. Stimulation duration will be titrated according to the study protocol and individual participant response. Participants will continue the pharmacotherapy regimen received before Phase 2. Medication doses will remain stable whenever clinically feasible; changes will be permitted only when clinically necessary for safety or tolerability and will be documented.
Outros nomes:
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O que o estudo está medindo?
Medidas de resultados primários
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
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PANSS reduction rate at Week 8 during the pharmacological optimization phase
Prazo: Baseline of pharmacological optimization phase and Week 8
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Percentage reduction in Positive and Negative Syndrome Scale total score from baseline to Week 8. The PANSS scale consists of 30 items, and each item is rated on a 7-point scale, ranging from 1 (no symptoms) to 7 (extremely severe). The PANSS reduction rate is calculated as: (baseline PANSS total score - Week 8 PANSS total score) / (baseline PANSS total score - 30) × 100%. |
Baseline of pharmacological optimization phase and Week 8
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PANSS reduction rate at Week 4 during the neuromodulation phase
Prazo: Baseline of neuromodulation phase and Week 4
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Percentage reduction in PANSS total score from baseline of the neuromodulation phase to Week 4. The PANSS scale consists of 30 items, and each item is rated on a 7-point scale, ranging from 1 (no symptoms) to 7 (extremely severe). The PANSS reduction rate is calculated as: (baseline PANSS total score - Week 4 PANSS total score) / (baseline PANSS total score - 30) × 100%. |
Baseline of neuromodulation phase and Week 4
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Medidas de resultados secundários
Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
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Change in CGI-S score
Prazo: Pharmacological optimization: baseline and Week 8; Neuromodulation: baseline and Week 4.
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Change in Clinical Global Impression-Severity (CGI-S) score from baseline to the end of assigned treatment. The scale provides an assessment of both disease severity and overall efficacy.The severity of the disease was scored on an eight-point scale ranging from 0 (not rated) to 7 (extremely severe). The overall efficacy was assessed on an 8-point scale ranging from 0 (not assessed) to 7 (significant deterioration). |
Pharmacological optimization: baseline and Week 8; Neuromodulation: baseline and Week 4.
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Trajectory of PANSS total score improvement during the neuromodulation phase
Prazo: Baseline of the neuromodulation phase and weekly during the 4-week neuromodulation treatment course
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Rate of change in Positive and Negative Syndrome Scale total score during the 4-week neuromodulation treatment course. The PANSS scale consists of 30 items, and each item is rated on a 7-point scale, ranging from 1 (no symptoms) to 7 (extremely severe). Repeated PANSS assessments will be used to compare the trajectory and speed of symptom improvement between the MECT and MST groups. |
Baseline of the neuromodulation phase and weekly during the 4-week neuromodulation treatment course
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Change in AMT specificity score during the neuromodulation phase
Prazo: Baseline of the neuromodulation phase and Week 4
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Change in Autobiographical Memory Test(AMT) specificity score from baseline of the neuromodulation phase to Week 4. The AMT specificity score is defined as the number of specific autobiographical memories retrieved in response to 12 cue words, with scores ranging from 0 to 12 and higher scores indicating better autobiographical memory specificity. Change is calculated as Week 4 AMT specificity score minus baseline AMT specificity score; negative values indicate decline in autobiographical memory specificity. |
Baseline of the neuromodulation phase and Week 4
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Change from baseline in cognitive function: MCCB
Prazo: Baseline, Month 1, and Month 2 during the pharmacological optimization phase; and Week 4 of the neuromodulation phase.
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MATRICS consensus cognitive battery (MCCB) consists of 10 tests that assess cognitive performance in 7 domains, including processing speed, attention/vigilance, working memory, verbal memory, visual learning, reasoning and problem solving, and social cognition.The MCCB T-score is calculated based on a Chinese community sample, with a normative mean of 50 and a standard deviation of 10. Higher scores indicate a better neurocognitive outcome. |
Baseline, Month 1, and Month 2 during the pharmacological optimization phase; and Week 4 of the neuromodulation phase.
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Change in visuospatial working memory during the neuromodulation phase
Prazo: Baseline of the neuromodulation phase and weekly during the 4-week neuromodulation phase
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Change in visuospatial working memory from baseline to Week 4, assessed using the Wechsler Memory Scale-III Spatial Span subtest (WMS III). The WMS III total score ranges from 0 to 32, with higher scores indicating better visuospatial working memory performance. |
Baseline of the neuromodulation phase and weekly during the 4-week neuromodulation phase
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Change in visual learning during the neuromodulation phase
Prazo: Baseline of the neuromodulation phase and weekly during the 4-week neuromodulation phase
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Change in visual learning from baseline to Week 4, assessed using the Brief Visuospatial Memory Test-Revised (BVMT-R).The BVMT-R total recall score ranges from 0 to 36, where higher scores indicate better visual learning ability. |
Baseline of the neuromodulation phase and weekly during the 4-week neuromodulation phase
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Change in personal and social functioning
Prazo: Baseline, Week 8 of the pharmacological optimization phase and Week 4 of the neuromodulation phase
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Change in Personal and Social Performance Scale(PSP) score from baseline to the end of the corresponding treatment phase.The PSP score ranges from 0 to 100, where higher scores indicate better personal and social functioning. |
Baseline, Week 8 of the pharmacological optimization phase and Week 4 of the neuromodulation phase
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Extrapyramidal adverse effects: The Barnes Akathisia Scale (BAS)
Prazo: Baseline, Week 4, Week 8 during the pharmacological optimization phase and Week 1, Week 2, Week 3, Week 4 during the neuromodulation phase
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The Barnes Akathisia Scale (BAS) will be used to evaluate objective performance and subjective experience of akathisia, scored from 0 to 3, and the overall clinical evaluation of akathisia is scored from 0 to 5. The higher scores mean a more serious side effect. |
Baseline, Week 4, Week 8 during the pharmacological optimization phase and Week 1, Week 2, Week 3, Week 4 during the neuromodulation phase
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Extrapyramidal adverse effects: Simpson-Angus Extrapyramidal Side Effects Scale (SAS)
Prazo: Baseline, Week 4, Week 8 during the pharmacological optimization phase and Week 1, Week 2, Week 3, Week 4 during the neuromodulation phase
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Simpson-Angus Extrapyramidal Side Effects Scale (SAS) consists of 10 items, each scored from 0 to 4. The higher scores mean a more serious side effect. |
Baseline, Week 4, Week 8 during the pharmacological optimization phase and Week 1, Week 2, Week 3, Week 4 during the neuromodulation phase
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Extrapyramidal adverse effects: Abnormal Involuntary Movement Scale (AIMS)
Prazo: Baseline, Week 4, Week 8 during the pharmacological optimization phase and Week 1, Week 2, Week 3, Week 4 during the neuromodulation phase
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Abnormal Involuntary Movement Scale (AIMS) consists of 12 items. The first 10 of 12 items is scored from 0 to 4, and the last 2 is scored from 0 to 1. The higher scores mean the more obvious abnormal involuntary movement. |
Baseline, Week 4, Week 8 during the pharmacological optimization phase and Week 1, Week 2, Week 3, Week 4 during the neuromodulation phase
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Colaboradores e Investigadores
Patrocinador
Patrocinador
Investigadores
Investigadores
- Investigador principal: DengTang Liu, Shanghai Mental Health Center
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Real)
Início do estudo
Conclusão Primária (Estimado)
Conclusão Primária
Conclusão do estudo (Estimado)
Conclusão do estudo
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Real)
Primeira postagem
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última Atualização Postada
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Última verificação
Mais Informações
Termos relacionados a este estudo
Termos MeSH relevantes adicionais
- Espectro da Esquizofrenia e Outros Transtornos Psicóticos
- Transtornos Mentais, Desordem Mental
- Esquizofrenia
- Esquizofrenia Resistente ao Tratamento
- Qualidade, acesso e avaliação da assistência médica
- Produtos químicos orgânicos
- Compostos heterocíclicos, 1 anel
- Compostos heterocíclicos
- Compostos heterocíclicos, 2 anel
- Compostos heterocíclicos, anel fundido
- Técnicas de investigação
- Métodos epidemiológicos
- Hidrocarbonetos
- Hidrocarbonetos, cíclicos
- Mecanismos de avaliação de saúde
- Qualidade de assistência médica
- Saúde pública
- Meio ambiente e saúde pública
- Ácidos carboxílicos
- Hidrocarbonetos, aromáticos
- Amidas
- Produtos químicos inorgânicos
- Compostos de cloro
- Derivados de benzeno
- Óxidos
- Compostos de oxigênio
- Ácidos, não carboxílico
- Ácidos
- Ácidos, carbocíclicos
- Quinolones
- Quinolinas
- Benzoates
- Espécies reativas de oxigênio
- Radicais livres
- Dibenzazepínicos
- Compostos heterocíclicos, 3 anel
- Benzamides
- Piperazinas
- Características do estudo epidemiológico
- Ensaios clínicos como tópico
- Estudos clínicos como tópico
- Aripiprazol
- Amissulprida
- Clozapina
- Ensaios clínicos, Fase I como tópico
- Ensaios Clínicos, Fase II como Tópico
- Ácido Hipocloroso
Outros números de identificação do estudo
Outros números de identificação do estudo
- 2025-SFDL01
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
Descrição do plano IPD
Individual participant data will not be shared because the study involves sensitive clinical, cognitive, imaging, and biological data from patients with schizophrenia, and data sharing is limited by participant consent and institutional ethics requirements. Only aggregate study results will be reported.
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