Playware Technology for Balance Training (IMT)

October 1, 2017 updated by: Jari Due Jessen, Technical University of Denmark

Efficacy of Interactive Modular Tiles Training Versus "Usual Care" on Physical Attributes Among Elder Adults 70+. A Randomized Controlled Trial

This study evaluates the use of Playware technology for balance training. Falling among elder is a costly problem. Research shows that training can help prevent falls. Pilot studies of the use of Interactive Modular Tiles (IMT) show that the participants can highly increase their physical abilities.

The interventions group will train using interactive modular tiles. The tiles include preprogrammed games that create playful training for the participants.

The control group will receive "usual care", which here refers to normal day activities.

The intervention will be done 2 times a week for 12 weeks, each session lasting 1 hour and each participant receiving 13 minutes of training each time.

Study Overview

Status

Completed

Conditions

Detailed Description

This study will investigate the use of one form of exergames called IMT how this compared to usual care of elderly people 70+. The trial will consist of two groups, one for training with the IMT and usual care that will receive the care provided to non-patients elderly, which at this moment is no additional treatment other than recommendations.

The study will be single blinded, randomized controlled trial. It will be funded by the patient@home project and Entertainment robotics. Concealed allocation and intention-to-treat analysis will be used. Measurements will be taken at baseline and after intervention. Upon acceptance the protocol will be registered in clinicaltrials.gov.

The trial's results will be reported using domains and categories described in the taxonomy developed by the Prevention of Falls Network Europe, to allow future synthesis of evidence, or study replication.

The intervention is done in the form of groups of 4-5 participants per set of tiles, with 2-3 set of tiles at a time. As more set can be used it is possible to make groups of more people. The training will consist of 1.5-3 minutes of training (depending on the game) on tiles and the rest while the other 2-3 participants train (4-6 minutes of break). Then the participants will train for 1.5-3 minutes again until each participant have received a total of 13 minutes of training.

The control group will not train.

Study Type

Interventional

Enrollment (Actual)

60

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

      • Kgs. Lyngby, Denmark, 2800
        • Technical University of Denmark

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

70 years and older (Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Community-dwelling
  • 70+ years

Exclusion Criteria:

  • A previous diagnosis of strong dementia or a cognitive decline that prevents the understanding of simple instructions or guidelines;
  • A previous stroke with a severe neurological impairment, such as loss of strength, and perceptual or language limitations;
  • A severe visual deficiency;
  • Inability to maintain a standing position, even with the use of a walking aid or other device;
  • Participating in rehabilitative training.

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: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Training

The intervention is done in the form of groups of 4-5 participants per set of tiles, with 2-3 set of tiles at a time. As more set can be used it is possible to make groups of more people. The training will consist of 1.5-3 minutes of training (depending on the game) on tiles and the rest while the other 2-3 participants train (4-6 minutes of break). Then the participants will train for 1.5-3 minutes again until each participant have received a total of 13 minutes of training.

The intervention will be done 2 times a week for 12 weeks, each session lasting 1 hour and each participant receiving 13 minutes of training each time (see training plan).

Training with the Interactive Modulare Tiles
No Intervention: Control
No training.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change From Baseline in Test Score of 6 Minute Walking Test at Week 14.
Time Frame: Baseline and at week 14
Numbers of meters that can be walked in 6 minutes around a 50-yard (45.7 meters) course. Baseline score compared to score at week 14.
Baseline and at week 14
Change From Baseline in Test Score of 30-second Chair Stand at Week 14.
Time Frame: Baseline and at week 14
Number of full stands that can be completed in 30 seconds with arms folded across chest. Baseline score compared to score at week 14.
Baseline and at week 14
Change From Baseline in Test Score of 8-Foot Up-and-Go at Week 14.
Time Frame: Baseline and at week 14
Number of seconds required to get up from a seated position, walk 8 feet (2.44 meters), turn, and return to seated position. Baseline score compared to score at week 14.
Baseline and at week 14

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change From Baseline in Test Score of Line Walk at Week 14.
Time Frame: Baseline and at week 14
Number of steps a person can do on a line directly after the foot without touching outside the line. Baseline score compared to score at week 14.
Baseline and at week 14
Change From Baseline in Test Score of Static Balance at Week 14.
Time Frame: Baseline and at week 14
Static Balance will be measured using Wii Balance Board, which have proven to be a valid measure of balance (Sgró 2014). This measure will be done using an application developed by Francesco Sgró and colleagues (Sgró 2014). Baseline score compared to score at week 14.
Baseline and at week 14
Adherence to Training, Composite Outcome Measure.
Time Frame: At week 14
Adherence to the training will be measured by registering the number of times the participants participate and how much they participate at each session.
At week 14
Motivation for Training
Time Frame: At week 14.
Semi-structured interviews will be done with the participant after the intervention to investigate the motivation of the IMT.
At week 14.
Acceptability of IMT
Time Frame: At week 14.
Semi-structured interviews will be done with the participant after the intervention to investigate the acceptability of the IMT
At week 14.

Collaborators and Investigators

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

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.

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

July 1, 2015

Primary Completion (Actual)

April 1, 2016

Study Completion (Actual)

May 1, 2016

Study Registration Dates

First Submitted

July 7, 2015

First Submitted That Met QC Criteria

July 10, 2015

First Posted (Estimate)

July 14, 2015

Study Record Updates

Last Update Posted (Actual)

July 13, 2018

Last Update Submitted That Met QC Criteria

October 1, 2017

Last Verified

October 1, 2017

More Information

Terms related to this study

Other Study ID Numbers

  • H-15006703

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.

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