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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04841161
Other study ID # KMUHIRB-F(II)-20150033
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 25, 2016
Est. completion date September 19, 2018

Study information

Verified date February 2021
Source Kaohsiung Medical University Chung-Ho Memorial Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The sit-to-stand and dynamic weight-shifting ability of stroke patients is highly associated with walking performance. Therefore, in order to improve the dynamic weight-shifting ability in sit-to-stand and parallel or tandem standing, a real-time visual or auditory feedback is used in our design to allow patients to realize the weight-bearing condition (by using load cells) in both sound and affected legs immediately. It can help patients to learn to control muscle to shift weight effectively which will improve patients' walking performance. By integrating physical therapy planning with electro-mechanical technology, the goal of this study is to develop a standing balance training system by requiring patients to control their center of pressure (COP) in performing sit-to-stand and maintain a standing posture via the use of their core and lower extremity musculature.


Description:

1. Written informed consent must be obtained before any study specific procedures are undertaken. 1. For healthy group: Participants will be recruited from the staffs and students in Kaohsiung Medical University (including Learning University), and healthy families of CVA patients in the university affiliated hospital. 2. For stroke (CVA) group: We will ask the physical therapists in the university affiliated hospital to nominate the potential CVA participants . The physicians will determine if they would meet the inclusion criteria before participating the present study. 2. The process of the experiment (brief describe) 1. Written informed consent must be obtained before any study specific procedures are undertaken. 2. Subjects who are recruited to participate in this experiment should provide the personal information forms first (ex: sex, age, height, weight, post-stroke duration, stroke type, hemiplegic side, ambulation devices etc.). Then, assessment (PASS, Berg Balance Scale, Timed Up and Go) will be conducted by a physical therapist at baseline. 3. While the stroke patients after completing the 4 -times, and 8-times training program, the above-mentioned assessment conducted again by the same physical therapist. The healthy will not receive balance training, thus .only receive one assessment.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date September 19, 2018
Est. primary completion date September 19, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 75 Years
Eligibility Inclusion Criteria: 1. Healthy adults a. Their age should be ranged between 20 - 75 years 2. Stroke patients 1. diagnosed with unilateral ischemic or hemorrhagic stroke 2. a minimum of six months post stroke 3. able to stand without support for 1 minutes 4. medically stable with physician release Exclusion Criteria: 1. Healthy adults 1. neurological diseases 2. musculoskeletal diseases 3. rheumatic diseases 4. history of orthopedic surgery on spine or lower extremity 2. Stroke patients 1. other injuries or illnesses that affect standing or walking

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Balance function, gait ability, weight- distribution and weight-shifting
Healthy adults and stroke patients accepted two measurements within a week. Balance function, gait ability, weight- distribution and weight-shifting during sit-to-stand, quite standing, and weight-shifting toward the forward foot.
Weight- distribution and weight-shifting training program
The stroke patients received a weight-shifting training program , 30 minutes/time, 2-5 days a week for 2-3 weeks(8 sessions). After training, they accepted a post-test within a week.

Locations

Country Name City State
Taiwan Li-Jiun Liaw Kaohsiung City Sanmin Dist

Sponsors (1)

Lead Sponsor Collaborator
Kaohsiung Medical University Chung-Ho Memorial Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Changes in performance of weight distribution after 8 sessions intervention By using the force plate to record the ground reaction force and then to obtain weight distribution while performing the sit to stand activity The assessments will be conducted before and after intervention (4 Weeks, 8 Sessions)
Primary Changes in performance of standing balance after 8 sessions intervention By using the force plate to obtain displacements of the center of pressure (COP) while standing and weight transfer The assessments will be conducted before and after intervention (4 Weeks, 8 Sessions)
Primary Changes in performance of static and dynamic balance after 8 sessions intervention By using the Postural Assessment Scale of Stroke (PASS) to assess and monitor postural control. The PASS consists of 2 sections with a 4-point scale to describe each task. The total score ranges from 0 - 36. The assessments will be conducted before and after intervention (4 Weeks, 8 Sessions)
Primary Changes in performance of balance function after 8 sessions intervention By using the Berg Balance Scale to assess balance function. It is a 14 item list with each item consisting of a five-point ordinal scale ranging from 0 to 4during a series of predetermined tasks. The total score ranges from 0 - 56. The assessments will be conducted before and after intervention (4 Weeks, 8 Sessions)
Primary Changes in performance of dynamic balance after 8 sessions intervention By using Timed Up and Go Test (TUG) to assess fall risk and measure the progress of balance. An older adult who takes =12 seconds to complete the TUG is at risk for falling. The assessments will be conducted before and after intervention (4 Weeks, 8 Sessions)
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