| Recruitment status | No longer recruiting |
| Unique ID issued by UMIN | UMIN000020051 |
| Receipt No. | R000023158 |
| Official scientific title of the study | Effect of stroke patients with hemiplegia with the gait rehabilitation training using the biofeedback device to share paralyzed-side foot contact of the patient on the back |
| Date of disclosure of the study information | 2015/12/03 |
| Last modified on | 2017/12/04 (Ver. 5) |
| Basic information | ||
| Official scientific title of the study | Effect of stroke patients with hemiplegia with the gait rehabilitation training using the biofeedback device to share paralyzed-side foot contact of the patient on the back | |
| Title of the study (Brief title) | Effect of stroke patients with hemiplegia with the gait rehabilitation training using the biofeedback device | |
| Region |
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| Condition | ||
| Condition | stroke | |
| Classification by specialty |
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| Classification by malignancy | Others | |
| Genomic information | NO | |
| Objectives | |
| Narrative objectives1 | We test the effect of the biofeedback device on stroke patients with hemiplegia |
| Basic objectives2 | Efficacy |
| Basic objectives -Others | |
| Trial characteristics_1 | |
| Trial characteristics_2 | |
| Developmental phase | |
| Assessment | |
| Primary outcomes | Gait speed(Immediately after intervention) |
| Key secondary outcomes | |
| Base | |
| Study type | Interventional |
| Study design | |
| Basic design | Parallel |
| Randomization | Randomized |
| Randomization unit | Individual |
| Blinding | Open -no one is blinded |
| Control | Active |
| Stratification | |
| Dynamic allocation | |
| Institution consideration | |
| Blocking | |
| Concealment | |
| Intervention | |||
| No. of arms | 3 | ||
| Purpose of intervention | Treatment | ||
| Type of intervention |
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| Interventions/Control_1 | Usual gait rehabilitation training(Use Period:None) | ||
| Interventions/Control_2 | Gait rehabilitation training patient's using the biofeedback device (Use Period: 1 day(15 min)) | ||
| Interventions/Control_3 | Gait rehabilitation training patient's and therapist's using the biofeedback device(Use Period: 1 day(15 min)) | ||
| Interventions/Control_4 | |||
| Interventions/Control_5 | |||
| Interventions/Control_6 | |||
| Interventions/Control_7 | |||
| Interventions/Control_8 | |||
| Interventions/Control_9 | |||
| Interventions/Control_10 | |||
| Eligibility | ||||
| Age-lower limit |
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| Age-upper limit |
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| Gender | Male and Female | |||
| Key inclusion criteria | Patient who agree to the clinical test and meet the following conditions.
1. Patient's recovery stage is Brunnstrom stage 3/4/5 2. The patient has no higher brain dysfunction. 3. Primary doctor and therapist allowed patients to the gait training. |
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| Key exclusion criteria | The patient has the following serious condition
1.Uncontrollable heart failure 2.Acute myocardial infarction 3.Myocarditis,pericarditis 4.Angina pectoris 5.Acute embolism, pulmonary embolism 6.Acute infection 7.Thrombophlebitis 8.Ventricular tachycardia, ventricular arrhythmia 9.Uncontrollable arterial hypertension, pulmonary hypertension |
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| Target sample size | 30 | |||
| Research contact person | |
| Name of lead principal investigator | Hiroyasu Iwata |
| Organization | Waseda university |
| Division name | Faculty science and engineering |
| Address | 27 Waseda-cyo, Shinjuku-ku, Tokyo 162-0044, Japan Green Computing Systems Reserch Organization 603 Prof. Iwata Lab. |
| TEL | 03-3203-4427 |
| jubi@waseda.jp | |
| Public contact | |
| Name of contact person | Hiroyasu Iwata |
| Organization | Waseda university |
| Division name | Faculty science and engineering |
| Address | 27 Waseda-cyo, Shinjuku-ku, Tokyo 162-0044, Japan Green Computing Systems Reserch Organization 603 P |
| TEL | 03-3203-4427 |
| Homepage URL | |
| jubi@waseda.jp | |
| Sponsor | |
| Institute | Waseda university |
| Institute | |
| Department | |
| Funding Source | |
| Organization | Grant-in-Aid for Scientific Research |
| Organization | |
| Division | |
| Category of Funding Organization | Japanese Governmental office |
| Nationality of Funding Organization | Japan |
| Other related organizations | |
| Co-sponsor | |
| Name of secondary funder(s) | |
| Secondary IDs | |
| Secondary IDs | NO |
| Study ID_1 | |
| Org. issuing International ID_1 | |
| Study ID_2 | |
| Org. issuing International ID_2 | |
| IND to MHLW | |
| Institutions | |
| Institutions | 総合東京病院(東京都) |
| Other administrative information | |||||||
| Date of disclosure of the study information |
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| Progress | |||||||
| Recruitment status | No longer recruiting | ||||||
| Date of protocol fixation |
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| Anticipated trial start date |
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| Last follow-up date | |||||||
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| Date trial data considered complete | |||||||
| Date analysis concluded | |||||||
| Related information | |
| URL releasing protocol | |
| Publication of results | Partially published |
| URL releasing results | |
| Results | |
| Other related information | |
| Management information | |||||||
| Registered date |
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| Last modified on |
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| Link to view the page | |
| URL(English) | https://upload.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000023158 |