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Trial · NCT02553993

Registered outcomes11

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryChange from Baseline in Cognitive Abilities Screening Instrument Scale Chinese version (CASI C-2.0)Subjects will be assesed at 12 weeks and 24 weeks
The CASI C-2.0 consists of 20 item sets, which can be divided into 9 domains, including long-term memory, short-term memory, attention, concentration or mental manipulation, orientation, abstraction/judgment, language, visual construction, and category fluency. The CASI scores range from 0 to 100, with higher scores indicating better cognitive performance.
SecondaryChange from Baseline in The Stroop testSubjects will be assesed at 12 weeks and 24 weeksThe Stroop test requires selective attention, response inhibition, and working memory. The Stroop score ranges from 0 to 63, with higher scores indicating better performance.
SecondaryChange from Baseline in The modified Trail Making Test(TMT)Subjects will be assesed at 12 weeks and 24 weeksThe modified Trail Making Test (TMT) requires visual scanning, visuo-motor tracking, divided attention, and cognitive flexibility. The shorter time to complete the test means better performance.
SecondaryChange from Baseline in The digit backward performanceSubjects will be assesed at 12 weeks and 24 weeksThe digit backward performance requires attention and working memory. The scores range from 2 to 7 higher scores indicating better performance.
SecondaryChange from Baseline in Physiological profile assessment(PPA)Subjects will be assesed at 12 weeks and 24 weeksThe PPA is a validated battery of sensorimotor measurements used to identify those subjects at risk of falling.
SecondaryChange from Baseline in The 10m walking testSubjects will be assesed at 12 weeks and 24 weeks
The 10m WT is a reliable, valid, and responsive measure for sub-acute stroke. Walking speed will be assessed by self-selected gait speed over 10 m. The shorter time it takes is indicating better performance.
SecondaryChange from Baseline in Tetrax balance systemSubjects will be assesed at 12 weeks and 24 weeksTetrax balance system will be used to assess static standing balance. The lower risk scores is indicating better performance.
SecondaryChange from Baseline in Timed Up and Go (TUG) testSubjects will be assesed at 12 weeks and 24 weeksTimed Up and Go (TUG) test will be used to assessed Dynamic balance function. The shorter time it take means better performance.
SecondaryChange from Baseline in The Frenchay Activities Index (FAI)Subjects will be assesed at 12 weeks and 24 weeks
The Frenchay Activities Index (FAI) was used as a measure of subjects' participation level. The 15-item index records the frequency of performing social activities as well as more complex activities of daily living (eg, domestic chores, outdoor mobility, leisure, gainful work). The FAI item score is based on the frequency with which an activity was performed, and ranges from 0 (low frequency) to 3 (high frequency). Ten items concern the past 3 months and 5 items concern the past 6 months. The FAI total score is the sum of item scores, and ranges from 0 (inactive) to 45 (highly active).
SecondaryChange from Baseline in Stroke Impact ScaleSubjects will be assesed at 12 weeks and 24 weeks
The Stroke Impact Scale (SIS) is a 59-item self-reported scale with good reliability, validity, and sensitivity to change. The SIS consists of 8 functional domains: strength, memory, emotion, communication, ADL/ instrumental ADL (IADL), mobility, hand function, and participation. The overall SIS score represents the average score of the 8 domains. Each item score ranges from 1 to 5. Each domain score has a range of 0 to 100 and is computed by using the following equation: Score =\[(Mean - 1)/(5 - 1)\] × 100. In this equation, the score is that of a particular domain, and the mean is the average of the item scores within that domain. A higher score on an item denotes better performance.
SecondaryChange from Baseline in Physical Activity Enjoyment Scale (PACES)Subjects will be assesed at 12 weeks and 24 weeksThe PACES is a 18-item and 7-point self-reported scale, and the higher score has more enjoyment of the training.

Source ClinicalTrials.govtrials-2026-11-12-0.4.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNone stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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