ID

36447

Descrição

Cardiovascular Rehabilitation Early After Stroke Using Feedback-controlled Robotics-assisted Treadmill Exercise; ODM derived from: https://clinicaltrials.gov/show/NCT01679600 Brief Summary: The propose of this study is to evaluate the feasibility and the clinical efficiency of feedback-controlled robotics-assisted treadmill exercise (RATE) technology for cardiovascular rehabilitation early after stroke. The investigators hypothesize that feedback-controlled RATE might be suitable and effective to improve cardiovascular fitness and functional carryover in non-ambulatory individuals with sub-acute stroke.

Link

https://clinicaltrials.gov/show/NCT01679600

Palavras-chave

Versões (1)
  1. 14/05/2019 14/05/2019 -
Titular dos direitos

Bern University of Applied Sciences

Transferido a

14 de maio de 2019

DOI

Para um pedido faça login.

Licença

Creative Commons BY-NC 3.0
Comentários do modelo :

Aqui pode comentar o modelo. Pode comentá-lo especificamente através dos balões de texto nos grupos de itens e itens.

Voltar para os comentários do modelo
Comentários do grupo de itens para :

Comentários do item para :

Para descarregar formulários, precisa de ter uma sessão iniciada. Por favor faça login ou registe-se gratuitamente.

Rehabilitation after Stroke using Treadmills NCT01679600

Inglês

Eligibility Criteria

1 Formulários  
  1. StudyEvent: Eligibility
    1. Eligibility Criteria
Inclusion Criteria
Descrição

Inclusion Criteria

Alias
UMLS CUI
C1512693
Does the participant have a clinical diagnosis of an initial supratentorial stroke?
Descrição

Supratentorial Stroke

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0332140
UMLS CUI [1,2]
C3842364
UMLS CUI [1,3]
C0441938
Is the participant ≤20 weeks post stroke at intervention onset?
Descrição

Intervention Onset

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C1548614
UMLS CUI [1,2]
C3842364
UMLS CUI [1,3]
C0332162
UMLS CUI [1,4]
C0184661
Is the participant's age ≥18 years?
Descrição

Age

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0001779
Does the participant have a functional ambulation category (fac) ≤3?
Descrição

Functional ambulation category

Tipo de dados

boolean

Alias
UMLS CUI [1]
C2137127
Does the participant have the ability to understand the procedures and provide informed consent?
Descrição

Informed Consent

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C1273101
UMLS CUI [1,2]
C0184661
UMLS CUI [1,3]
C0021430
Exclusion Criteria
Descrição

Exclusion Criteria

Alias
UMLS CUI
C0680251
Does the participant have contraindications for exercise testing outlined by american college of sports medicine (acsm)?
Descrição

Exercise testing contraindications

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0015260
UMLS CUI [1,3]
C4264346
Does the participant have contraindications for rate according to the manufacturer?
Descrição

Rate Contraindications

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C1521828
UMLS CUI [1,3]
C0947322
Does the participant have concurrent neurological disease?
Descrição

Concurrent neurological disease

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0205420
UMLS CUI [1,2]
C0027765
Does the participant have concurrent pulmonary disease?
Descrição

Concurrent pulmonary disease

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0205420
UMLS CUI [1,2]
C0024115
Does the participant have a history of dementia?
Descrição

Dementia

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0497327
Voltar ao início da página

Similar models

Eligibility Criteria

1 Formulários
  1. StudyEvent: Eligibility
    1. Eligibility Criteria
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
C1512693 (UMLS CUI)
Supratentorial Stroke
Item
Does the participant have a clinical diagnosis of an initial supratentorial stroke?
boolean
C0332140 (UMLS CUI [1,1])
C3842364 (UMLS CUI [1,2])
C0441938 (UMLS CUI [1,3])
Intervention Onset
Item
Is the participant ≤20 weeks post stroke at intervention onset?
boolean
C1548614 (UMLS CUI [1,1])
C3842364 (UMLS CUI [1,2])
C0332162 (UMLS CUI [1,3])
C0184661 (UMLS CUI [1,4])
Age
Item
Is the participant's age ≥18 years?
boolean
C0001779 (UMLS CUI [1])
Functional ambulation category
Item
Does the participant have a functional ambulation category (fac) ≤3?
boolean
C2137127 (UMLS CUI [1])
Informed Consent
Item
Does the participant have the ability to understand the procedures and provide informed consent?
boolean
C1273101 (UMLS CUI [1,1])
C0184661 (UMLS CUI [1,2])
C0021430 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Exercise testing contraindications
Item
Does the participant have contraindications for exercise testing outlined by american college of sports medicine (acsm)?
boolean
C1301624 (UMLS CUI [1,1])
C0015260 (UMLS CUI [1,2])
C4264346 (UMLS CUI [1,3])
Rate Contraindications
Item
Does the participant have contraindications for rate according to the manufacturer?
boolean
C1301624 (UMLS CUI [1,1])
C1521828 (UMLS CUI [1,2])
C0947322 (UMLS CUI [1,3])
Concurrent neurological disease
Item
Does the participant have concurrent neurological disease?
boolean
C0205420 (UMLS CUI [1,1])
C0027765 (UMLS CUI [1,2])
Concurrent pulmonary disease
Item
Does the participant have concurrent pulmonary disease?
boolean
C0205420 (UMLS CUI [1,1])
C0024115 (UMLS CUI [1,2])
Dementia
Item
Does the participant have a history of dementia?
boolean
C0262926 (UMLS CUI [1,1])
C0497327 (UMLS CUI [1,2])
Voltar ao início da página 

Contacto

Use este formulário para feedback, perguntas e sugestões de aperfeiçoamento.

Campos marcados com * são obrigatórios.

Ajuda

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial