Simulation-Based Patient Education to Address Radiotherapy-Related Anxiety in Cancer Patients (ARAISE) (ARAISE)
Addressing Radiotherapy Anxiety Through Immersive Simulation and Education: Effects of a Simulation-Based Patient Education Intervention on Psychosocial Burden in Cancer Patients Receiving Radiotherapy (ARAISE)
Visão geral do estudo
Status
Status
Condições
Condições
Intervenção / Tratamento
Intervenção / Tratamento
Descrição detalhada
Tipo de estudo
Tipo de estudo
Inscrição (Estimado)
Inscrição
Estágio
Estágio
- Não aplicável
Contactos e Locais
Contato de estudo
Contato de estudo
- Nome: Rami El Shafie, Prof. Dr. med
- Número de telefone: +49 551 3964501
- E-mail: rami.elshafie@med.uni-goettingen.de
Estude backup de contato
- Nome: Stephan-Peter Landgraff, M.Ed.
- Número de telefone: +49 30 76 68 37 5 600
- E-mail: stephan.landgraff@medicalschool-berlin.de
Locais de estudo
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Lower Saxony
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Göttingen, Lower Saxony, Alemanha, 37075
- Department of Radiotherapy and Radiation Oncology, University Medical Center Goettingen
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Contato:
- Stephan-Peter Landgraff, M.Ed.
- Número de telefone: +49 5513964501
- E-mail: stephan.landgraff@medicalschool-berlin.de
-
Contato:
- Rami El Shafie, Prof. Dr. med.
- Número de telefone: +49 5513964501
- E-mail: rami.elshafie@med.uni-goettingen.de
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Investigador principal:
- Rami El Shafie, Prof. Dr. med.
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Critérios de participação
Critérios de elegibilidade
Critérios de elegibilidade
Idades elegíveis para estudo
- Adulto
- Adulto mais velho
Aceita Voluntários Saudáveis
Descrição
Inclusion Criteria:
- Age 18 years or older
- Histologically or cytologically confirmed malignant tumor disease
- Stage I - III (UICC TNM classification)
- ECOG performance status ≤ 2
- Curative-intent external beam radiotherapy regimen with at least 5 fractions
- First course of radiotherapy
- Able to independently operate the electronic data collection instrument
- Written informed consent after study information
- Sufficient German language proficiency to read and complete the study questionnaires independently and without translation assistance
Exclusion Criteria:
- Lack of capacity to provide informed consent
- Pregnancy or breastfeeding
- Stereotactic radiotherapy
- Emergency treatment indication
- Acute suicidality, acute psychosis, or other acute psychiatric disorder
- Initiation of or dose change in psychotropic medication within 4 weeks before baseline (T0)
- Cognitive impairment that precludes independent completion of the questionnaires
- Visual or auditory impairment that prevents perception of the on-screen or audio content despite available aids
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Cuidados de suporte
- Alocação: Randomizado
- Modelo Intervencional: Atribuição Paralela
- Mascaramento: Nenhum (rótulo aberto)
Número de braços
Armas e Intervenções
Grupo de Participantes / BraçoGrupo de Participantes / Braço |
Intervenção / TratamentoIntervenção / Tratamento |
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Sem intervenção: Standard Patient Education
Participants receive standard patient education before radiotherapy according to routine clinical practice.
Standard patient education comprises the physician consultation covering the indication and aim of radiotherapy, treatment planning and delivery, possible acute and late side effects, and organizational aspects of care.
No simulation-based education session is provided.
Prescribed oncological treatment and routine radiotherapy care are not altered.
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Experimental: Simulation-Based Patient Education
Participants receive standard patient education as in the control arm and, in addition, a single structured simulation-based patient education session after the planning CT and before the first radiotherapy fraction.
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A single, standardized, simulation-based patient education session lasting 15 to 20 minutes, conducted in addition to the standard education session that takes place after the planning CT scan and before the first radiation therapy fraction.
This session uses the immersive radiation therapy simulation software VERT 9.0 to visualize the treatment room, the linear accelerator, and the treatment process.
In addition to illustrating the treatment process, targeted information is provided to address treatment-specific fears identified as priorities in the Delphi consensus.
The session is conducted by the principal investigator following a standardized procedure to ensure comparability among participants.
The prescribed oncological treatment and routine radiation therapy remain unchanged.
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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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State anxiety at the first radiotherapy fraction (STAI-G Form X1)
Prazo: First radiotherapy fraction (T2), approximately 2 weeks after randomization
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State anxiety at the first radiotherapy fraction (T2), measured with the state scale (Form X1) of the German version of the State-Trait Anxiety Inventory (STAI-G).
The sum score comprises 20 items and ranges from 20 to 80, with higher scores indicating greater state anxiety.
The adjusted between-group difference in means at T2 is analyzed by analysis of covariance with the baseline state anxiety score at T0 as a continuous covariate and dichotomized trait anxiety at T0 as a factor.
The effect measure is the adjusted mean difference with a 95% confidence interval.
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First radiotherapy fraction (T2), approximately 2 weeks after randomization
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Medidas de resultados secundários
Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
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State anxiety after the planning CT or education session (STAI-G Form X1)
Prazo: T1, immediately after the planning CT or after the education session, approximately 1 week after randomization
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State anxiety at T1, measured with the state scale (Form X1) of the German version of the State-Trait Anxiety Inventory (STAI-G).
Scores range from 20 to 80, with higher scores indicating greater state anxiety.
Analyzed by analysis of covariance with the baseline state anxiety score at T0 as a continuous covariate and dichotomized trait anxiety at T0 as a factor.
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T1, immediately after the planning CT or after the education session, approximately 1 week after randomization
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State anxiety at the fifth radiotherapy fraction (STAI-G Form X1)
Prazo: Fifth radiotherapy fraction (T3), approximately 3 weeks after randomization
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State anxiety at T3, measured with the state scale (Form X1) of the German version of the State-Trait Anxiety Inventory (STAI-G).
Scores range from 20 to 80, with higher scores indicating greater state anxiety.
Analyzed by analysis of covariance with the baseline state anxiety score at T0 as a continuous covariate and dichotomized trait anxiety at T0 as a factor.
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Fifth radiotherapy fraction (T3), approximately 3 weeks after randomization
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Health-related quality of life: Global Health Status/Quality of Life (EORTC QLQ-C30)
Prazo: Fifth radiotherapy fraction (T3), approximately 3 weeks after randomization
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Health-related quality of life at T3, measured with the EORTC QLQ-C30 and linearly transformed to a score from 0 to 100, with higher scores indicating a greater global health status and quality of life.
Analyzed by analysis of covariance with group as a factor, the T0 Global Health Status/Quality of Life score as a continuous covariate, and dichotomized trait anxiety at T0 as a factor.
Functioning and symptom scales are reported descriptively only.
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Fifth radiotherapy fraction (T3), approximately 3 weeks after randomization
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Perceived amount of information received: "Information about the treatment" scale (EORTC QLQ-INFO25)
Prazo: T1, immediately after the planning CT or after the education session, approximately 1 week after randomization
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Perceived amount of information received at T1, measured with the multi-item scale "Information about the treatment" (items 38 to 43) of the EORTC QLQ-INFO25 and linearly transformed to a score from 0 to 100, with higher scores indicating a greater perceived amount of information.
Groups are compared in a linear model with group as a factor and dichotomized trait anxiety at T0 as the only adjustment variable.
The remaining multi-item scales, single items, the total score, and the assessment at T2 are reported descriptively.
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T1, immediately after the planning CT or after the education session, approximately 1 week after randomization
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Feasibility of the simulation-based patient education intervention
Prazo: From enrollment to the fifth radiotherapy fraction (T3), approximately 3 weeks per participant
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Composite descriptive endpoint with target values defined a priori: recruitment rate of at least 50%, retention rate of at least 80% at T3, protocol adherence of at least 90%, data completeness of at least 85% from T0 to T3, and tolerability defined as discontinuation due to intervention-associated distress reactions in no more than 10% of participants.
All rates are reported with two-sided 95% confidence intervals.
No formal hypothesis testing is performed.
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From enrollment to the fifth radiotherapy fraction (T3), approximately 3 weeks per participant
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Outras medidas de resultado
Outras medidas de resultado
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
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Moderation of the intervention effect on state anxiety at T2 by trait anxiety
Prazo: First radiotherapy fraction (T2), approximately 2 weeks after randomization
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Dispositional trait anxiety is measured once at baseline (T0) with the trait scale (Form X2) of the German version of the State-Trait Anxiety Inventory (STAI-G) and dichotomized at a threshold of 40 points or higher.
The group-by-trait-anxiety interaction term is tested in the analysis of covariance model of the primary endpoint (state anxiety at T2). Dichotomized trait anxiety additionally serves as a stratification factor for randomization and as a prognostic factor in all analyses of state anxiety.
This analysis is not independently powered and is interpreted as hypothesis-generating.
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First radiotherapy fraction (T2), approximately 2 weeks after randomization
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Effect modification of the primary endpoint by prespecified participant and treatment characteristics
Prazo: First radiotherapy fraction (T2), approximately 2 weeks after randomization
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Effect modification of state anxiety at T2 by irradiation site (central nervous system, head and neck, breast, thorax, abdomen, pelvis), sex, educational level, and concomitant systemic therapy, assessed via the respective interaction terms with treatment allocation in the model of the primary endpoint.
These analyses are not independently powered and are interpreted as hypothesis-generating.
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First radiotherapy fraction (T2), approximately 2 weeks after randomization
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Colaboradores e Investigadores
Patrocinador
Patrocinador
Colaboradores
Colaboradores
Investigadores
Investigadores
- Investigador principal: Rami El Shafie, Prof. Dr. med., Department of Radiotherapy and Radiation Oncology, University Medical Center Goettingen (UMCG)
- Diretor de estudo: Stephan-Peter Landgraff, M.Ed., Faculty of Health Sciences, Medical School Berlin (MSB)
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Estimado)
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
Palavras-chave
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
Outros números de identificação do estudo
- ARAISE-RT-UMG-2026
Plano para dados de participantes individuais (IPD)
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Descrição do plano IPD
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