Effect of Positive-word Stimuli on the Limits of Stability During Multi-direction Reach Operation in Standing Position

July 3, 2018 updated by: Kazuki Hirao, PhD, OT, Kibi International University

Immediate Effect of Positive-word Stimuli on the Limits of Stability During Multi-direction Reach Operation in Standing Position: A Randomized Controlled Superiority Trial

The purpose of the study was to examine the immediate effect of positive-word stimuli on the limits of stability during multi-direction reach operation in standing position in healthy young adults.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

62

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Japan
    • Okayama
      • Takahashi, Okayama, Japan
        • Kibi International University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 24 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

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

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Smartphone Application (SPSRS)
Participants watch motion picture using an application that displays positive-word stimuli.
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.
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.
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.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
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
Baseline and immediately after the intervention protocol

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Kibi International University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 6, 2018

Primary Completion (Actual)

June 14, 2018

Study Completion (Actual)

June 14, 2018

Study Registration Dates

First Submitted

May 22, 2018

First Submitted That Met QC Criteria

June 2, 2018

First Posted (Actual)

June 6, 2018

Study Record Updates

Last Update Posted (Actual)

July 6, 2018

Last Update Submitted That Met QC Criteria

July 3, 2018

Last Verified

July 1, 2018

More Information

Terms related to this study

Other Study ID Numbers

  • 18-16

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Healthy

Clinical Trials on Smartphone Application (SPSRS)

Search Similar Trials

Sponsors and Collaborators

Medical Conditions

Drug Interventions

CROs by country

CROs in Romania

Conditions

Rare Diseases

Drug Interventions

Dietary Supplements

Sponsor/Collaborators

Locations

3
Subscribe