Effect of Positive-word Stimuli on the Limits of Stability During Multi-direction Reach Operation in Standing Position
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| ClinicalTrials.gov Identifier: NCT03546218 |
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Recruitment Status :
Completed
First Posted : June 6, 2018
Last Update Posted : July 6, 2018
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Healthy | Device: Smartphone Application (SPSRS) Device: Smartphone Application (YouTube) | Not Applicable |
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 62 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | Single (Outcomes Assessor) |
| Primary Purpose: | Treatment |
| Official Title: | Immediate Effect of Positive-word Stimuli on the Limits of Stability During Multi-direction Reach Operation in Standing Position: A Randomized Controlled Superiority Trial |
| Actual Study Start Date : | June 6, 2018 |
| Actual Primary Completion Date : | June 14, 2018 |
| Actual Study Completion Date : | June 14, 2018 |
| Arm | Intervention/treatment |
|---|---|
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Experimental: Smartphone Application (SPSRS)
Participants watch motion picture using an application that displays positive-word stimuli.
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Device: Smartphone Application (SPSRS)
Participants use application on iPhone and watch videos showing positive-word stimuli. This application repeats positive-word stimuli every 5 seconds. The participants watch 3-minute motion picture displaying positive-word stimuli. |
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Active Comparator: Smartphone Application (YouTube)
Participants will watch the same motion picture as the experimental group. However, a positive-word stimulus does not appear in the motion picture.
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Device: Smartphone Application (YouTube)
Participants will watch the same motion picture as the experimental group. However, a positive-word stimulus does not appear in the motion picture. |
- Multi-Directional Reach Test [ Time Frame: Baseline and immediately after the intervention protocol ]The limits of stability during multi-direction reach operation in standing position
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| Ages Eligible for Study: | 18 Years to 24 Years (Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- Healthy volunteers between 18 and 24 years of age
- Males and Females
Exclusion Criteria:
- Person with physical disability that is enough to interfere with daily life
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03546218
| Japan | |
| Kibi International University | |
| Takahashi, Okayama, Japan | |
| Responsible Party: | Kazuki Hirao, PhD, OT, Assistant Professor, Kibi International University |
| ClinicalTrials.gov Identifier: | NCT03546218 |
| Other Study ID Numbers: |
18-16 |
| First Posted: | June 6, 2018 Key Record Dates |
| Last Update Posted: | July 6, 2018 |
| Last Verified: | July 2018 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |

