Trial · NCT02364232
Registered outcomes31
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
1 to 20 of 31
Download this page as JSON| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Fugl-Myer Assessment, FMA | Change from baseline up to 4 weeks immediately after the completion of intervention, and change from 4 weeks up immediately after the completion of intervention up to 3 months after the completion of intervention. | |
| Primary | Mini-Mental State Exam, MMSE | Change from baseline up to 4 weeks immediately after the completion of intervention | |
| Primary | pinch and grasp dynamometer | Change from baseline up to 4 weeks immediately after the completion of intervention, and change from 4 weeks up immediately after the completion of intervention up to 3 months after the completion of intervention. | |
| Primary | Modified Ashworth Scale, MAS | Change from baseline up to 4 weeks immediately after the completion of intervention, and change from 4 weeks up immediately after the completion of intervention up to 3 months after the completion of intervention. | |
| Primary | Revised Nottingham Sensory Assessment | Change from baseline up to 4 weeks immediately after the completion of intervention | |
| Primary | 10-Meter Walking Test, 10MWT | Change from baseline up to 4 weeks immediately after the completion of intervention | |
| Primary | Box and Block Test, BBT | Change from baseline up to 4 weeks immediately after the completion of intervention | |
| Primary | Wolf Motor Function Test, WMFT | Change from baseline up to 4 weeks immediately after the completion of intervention | |
| Primary | Chedoke Arm and Hand Activity Inventory | Change from baseline up to 4 weeks immediately after the completion of intervention | |
| Primary | Canadian Occupational Performance Measure, COPM | Change from baseline up to 4 weeks immediately after the completion of intervention | |
| Primary | Nottingham Extended Activities of Daily Living, NEADL | Change from baseline up to 4 weeks immediately after the completion of intervention, and change from 4 weeks up immediately after the completion of intervention up to 3 months after the completion of intervention. | |
| Primary | ABILHAND Questionnaire | Change from baseline up to 4 weeks immediately after the completion of intervention, and change from 4 weeks up immediately after the completion of intervention up to 3 months after the completion of intervention. | |
| Primary | Motor Activity Log, MAL | Change from baseline up to 4 weeks immediately after the completion of intervention, and change from 4 weeks up immediately after the completion of intervention up to 3 months after the completion of intervention. | |
| Primary | Actigraphy | Change from baseline up to 4 weeks immediately after the completion of intervention | |
| Primary | Stroke Impact Scale, SIS | Change from baseline up to 4 weeks immediately after the completion of intervention, and change from 4 weeks up immediately after the completion of intervention up to 3 months after the completion of intervention. | |
| Primary | The World Health Organization Quality of Life -Brief version, WHOQOL-BRE | Change from baseline up to 4 weeks immediately after the completion of intervention | |
| Primary | Medical Research Council scale,MRC | Change from baseline up to 4 weeks immediately after the completion of intervention | |
| Primary | 6 minute walk test | Change from baseline up to 4 weeks immediately after the completion of intervention | |
| Primary | The Euroqol Quality of Life Scale | Change from baseline up to 4 weeks immediately after the completion of intervention, and change from 4 weeks up immediately after the completion of intervention up to 3 months after the completion of intervention. | |
| Primary | Lawton-Brody IADL Scale | Change from baseline up to 4 weeks immediately after the completion of intervention |
Source ClinicalTrials.govtrials-2026-11-12-0.5.0
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license 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.
For software
Read this list from software.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/trials/v1/NCT02364232/registered