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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03282734
Other study ID # 2017-07-072
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 18, 2017
Est. completion date December 31, 2019

Study information

Verified date March 2020
Source Samsung Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A lot of patients suffer the balance and gait disorders after stroke. Many rehabilitation therapies have been provided to improve the balance and gait function in stroke patients. However, most rehabilitation therapies are performed in only hospitals, in spite of the difficulty of moving from home to hospitals for stroke patients. Home-based smart rehabilitation system (Uincare®, D-gate Co.) can provide the specific rehabilitation training program to stroke patients in their home. This study aims to investigate the effects of the home-based exercise program with smart rehabilitation system on balance and gait functions in stroke patients.


Description:

The total 100 patients with stroke will be divided into each the intervention group and the control group. The intervention group will be provided the home-based smart rehabilitation system for 4 weeks, and the control group will be educated the conventional home rehabilitation exercise at once. The immediate effects of the home-based smart rehabilitation system on the balance and gait function will be assessed at 4 weeks after exercise and the long-term carry-over effects will be also assesed at 4 weeks after cessation of exercise.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date December 31, 2019
Est. primary completion date June 30, 2018
Accepts healthy volunteers No
Gender All
Age group 19 Years and older
Eligibility Inclusion Criteria:

- adult stroke patients (more than 18 years old)

- less than 6 months after stroke onset

- discharged to home or the plan to discharge to home less than 3 days

- independent ambulatory function on even level (4 or more than 4 in Functional Ambulatory Category)

Exclusion Criteria:

- Advanced liver, kidney, cardiac, or pulmonary disease

- A terminal medical diagnosis consistent with survival < 1 year)

- Pre-existing and active major neurological disease

- Pre-existing and active major psychiatric disease

- Severe language disorders

- Severe cognitive disorders (10 or less than 10 in K-MMSE)

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Home-based exercise program with smart rehabilitation system ((Uincare®, D-gate Co.)
Home-based exercise program with smart rehabilitation system ((Uincare®, D-gate Co.) for more than 30 minutes per a day for 4 weeks
Conventional home rehabilitation exercise
Conventional home rehabilitation exercise for more than 30 minutes per a day for 4 weeks

Locations

Country Name City State
Korea, Republic of Samsung Medical Center Seoul

Sponsors (1)

Lead Sponsor Collaborator
Samsung Medical Center

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Timed Up and Go test Assessment of balance and gait function Change from baseline Timed Up and Go test at 4 weeks
Secondary Tinetti Performance Oriented Mobility Assessment Assessment of balance and gait function Change from baseline Timed Up and Go test at 4 weeks
Secondary Berg Balance scale Assessment of balance Change from baseline Timed Up and Go test at 4 weeks
Secondary Korean-Geriatric Depression Scale- Short Form Assessment of mood Change from baseline Timed Up and Go test at 4 weeks
Secondary EQ-5D Assessment of quality of life Change from baseline Timed Up and Go test at 4 weeks
Secondary Falls Efficacy Scale Assessment of fall risk Change from baseline Timed Up and Go test at 4 weeks
Secondary Korean version of Physical Activity Scale for the Elderly Assessment of physical activity Change from baseline Timed Up and Go test at 4 weeks
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