- ICH GCP
- Registro de ensaios clínicos dos EUA
- Ensaio Clínico NCT01035606
Training in Goal-directed Attention Regulation for Individuals With Brain Injury
Plasticity in Brain Network to Enhance Cognitive Rehabilitation
Visão geral do estudo
Status
Condições
Descrição detalhada
Tipo de estudo
Inscrição (Real)
Estágio
- Não aplicável
Contactos e Locais
Locais de estudo
-
-
California
-
Sacramento, California, Estados Unidos, 95655
- VA Northern California Health Care System, Mather, CA
-
-
Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
Aceita Voluntários Saudáveis
Gêneros Elegíveis para o Estudo
Descrição
Inclusion Criteria:
- history of traumatic brain injury
- greater than 1 week from injury
- residual dysfunction related to attention and executive control
Exclusion Criteria:
- aphasia
- active illicit drug use
- severe depression
- contraindications to MRI scanning
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Tratamento
- Alocação: Randomizado
- Modelo Intervencional: Atribuição Paralela
- Mascaramento: Nenhum (rótulo aberto)
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
|
Experimental: Goal-oriented Attention Regulation Training
training in goal-directed attention regulation
|
training in goal-directed attention regulation
|
|
Comparador Ativo: Education
brain health education
|
brain health education workshops
|
|
Experimental: Technology-assisted Goal-directed Self-Regulation Training
computer-assisted training in goal-directed attention regulation
|
computer-assisted training in goal-directed attention regulation, with trainer guidance and cognitive games to practice skills
|
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Self-report
Prazo: 5 Weeks (After completion of active trainings in Arm 1 and Arm 3)
|
Responses to goal processing questionnaire relating to areas of personal goal-based functioning.
This scale measured participants self-perceived changes to their cognitive and emotional functioning.
Participants indicated the degree to which they perceived changes to 11 questions after receiving trainings in Arm 1 and Arm 3 on a 10-point scale (1=domain became worse, 5 = no change, 10 = domain improved).
Participants did not complete this measure after Arm 2.
|
5 Weeks (After completion of active trainings in Arm 1 and Arm 3)
|
Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Change From Baseline to Post-training for Task Errors on a Functional Performance Measure
Prazo: 5 weeks (After completion of Arm 1 and Arm 2)
|
Participants completed a functional assessment task, the modified Multiple Errands Task (MET).
The MET is an unstructured functional task that permits assessment of participants' abilities to follow outlined rules and complete multiple 'real-world' tasks in a limited time period.
Participants were provided written instructions and a map of the hospital where the assessment took place, and were instructed to complete 12 subtasks in 40 minutes while following 9 specified rules.
Participants completed this at task at baseline and following Training (Arms 1 & 2, but not 3).
Outcome measure was computed as post-training - baseline (negative value reflects less errors made post-training).
|
5 weeks (After completion of Arm 1 and Arm 2)
|
|
Change to Attention and Executive Functioning Composite Scores
Prazo: 5 weeks (After completion of Arm 1 and Arm 2)
|
Participants completed the following neuropsychological measures of attention and executive functions before and after Arms 1 and 2, but not Arm 3. Letter Number Sequencing from WIAT-III; Auditory Consonant Trigram: 9,18, 36 seconds; Digit Vigilance Test (Time and Errors); DKEFS subtests: Design Fluency, Verbal Fluency Switching, Inhibition (Time and Errors); and Inhibition/Switching (Time and Errors); and Trails B. Performance on these measures were scored based upon age, and when available, educational and repeated administration norms. Resultant scores were transformed into z-scores and aggregated to form a composite measure. Higher z-scores reflect better functioning. The unit of analysis for this outcome was the change score from baseline to post-training. Positive change scores reflect improved performance over time[post-training - baseline], whereas negative change scores reflect worsening performance over time. |
5 weeks (After completion of Arm 1 and Arm 2)
|
Colaboradores e Investigadores
Patrocinador
Colaboradores
Investigadores
- Investigador principal: Mark D'Esposito, MD, VA Northern California Health Care System, Mather, CA
Publicações e links úteis
Publicações Gerais
- Chen AJ, Novakovic-Agopian T, Nycum TJ, Song S, Turner GR, Hills NK, Rome S, Abrams GM, D'Esposito M. Training of goal-directed attention regulation enhances control over neural processing for individuals with brain injury. Brain. 2011 May;134(Pt 5):1541-54. doi: 10.1093/brain/awr067. Epub 2011 Apr 22.
- Novakovic-Agopian T, Chen AJ, Rome S, Abrams G, Castelli H, Rossi A, McKim R, Hills N, D'Esposito M. Rehabilitation of executive functioning with training in attention regulation applied to individually defined goals: a pilot study bridging theory, assessment, and treatment. J Head Trauma Rehabil. 2011 Sep-Oct;26(5):325-38. doi: 10.1097/HTR.0b013e3181f1ead2.
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo
Conclusão Primária (Real)
Conclusão do estudo (Real)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Estimativa)
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- B4605-I
Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .