Feasibility of a Tablet-based Fall Prevention Program for Older Adults

March 26, 2018 updated by: Courtney D. Hall, East Tennessee State University
There are many exercise approaches that have demonstrated effectiveness in reducing falls and fall risk in community-dwelling older adults. The Otago Exercise Program is one such program. The Otago Exercise Program has been tested in four randomized controlled trials and one controlled multi-center trial and was found to reduce falls in older men and women. The focus of the Otago Exercise Program is on improving strength and balance with a home-based balance exercise program. The goal of the current study is to evaluate whether a self-administered, tablet-based version of the Otago fall prevention program is both feasible and effective for reducing fall risk and improving balance in community-dwelling older adults.

Study Overview

Status

Completed

Conditions

Detailed Description

Twenty community-dwelling older adults who satisfy the study criteria will be recruited to participate in this study. This group of participants will be selected to represent the general community-dwelling older adults as much as possible. They will demonstrate a range of ability in terms of their balance and mobility in which some are non-fallers and some fallers. All adults who meet the inclusion/exclusion criteria and have access to the internet via wireless connection will be included.

Participants will be consented for the research study and will be assessed initially, after 1 month of exercise and at the end of 2 months of exercise. Assessment will include questionnaires about health history, including falls, physical activity, balance confidence and system usability. Participants will also complete strength, balance and mobility physical performance tests. Age, sex, presence of comorbidities, medication list, functional abilities, balance confidence, fear of fall behavior and fall history will be assessed by questionnaire. Usability of the tablet-based questionnaire will be assessed by questionnaire. Participants will be tested with standard clinical tests of balance and gait.

Participants will be closely supervised by a Doctor of Physical Therapy (DPT) student during training in how to use the exercise program. Participants will complete a full set of exercises with the tablet in the presence of the DPT student. The DPT student will determine whether participants are safe with the program before allowing them to perform the program on their own at home. If the research team determines that a participant is unable to exercise safely on his/her own he/she will be withdrawn from the study.

The tablet-based, video game exercise program is called Health in Motion and was developed by Blue Marble Game Company. Health in Motion was tested in a pilot study and found to reduce fall risk in 8 of 15 older participants without any adverse events. Participants will complete 2 months of the home-based balance exercise program using the Health in Motion app. Participants will be asked to perform the exercises for 30 minutes 3x/week. Participants will be asked to perform the exercise program for 2 months.

Performance scores from the clinical gait and balance measures obtained during the initial visit will be compared to the performance scores obtained after 1 month and 2 months of performing the exercise program. We hypothesize that balance and gait will improve following 2 months of performing the tablet-based fall prevention exercise program at home. The assessments performed by the DPT students and by the participant using the app will be compared. We hypothesize that the scores from self-assessment will closely correlate to the students' assessment. The system usability score will be examined to understand issues associated with using technology. We hypothesize that older adults will enjoy performing the exercises using the tablet format.

Study Type

Interventional

Enrollment (Actual)

11

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

    • Tennessee
      • Johnson City, Tennessee, United States, 37614
        • East Tennessee State 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

60 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • age at least 60 years, ability to ambulate household distance without an assistive device; and ability to stand independently for twenty minutes

Exclusion Criteria:

  • cognitive impairment (based on Mini Mental Status Exam), unstable medical condition, progressive neurological condition, severe pain with weight bearing, and severe vision impairment

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: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Tablet-based Fall Prevention
The exercise program will be self-administered via a tablet-based version of the fall prevention program and the exercises performed in the home.
The focus of the Otago Exercise Program is on improving strength and balance with a home-based balance exercise program. The program will be self-administered via tablet-based version of the Otago fall prevention program. Participants will complete 2 months of the home-based balance exercise program using the Health in Motion app. Participants will be asked to perform the exercises for 30 minutes 3x/week. Participants will be asked to perform the exercise program for 2 months.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Activity-specific balance confidence (ABC)
Time Frame: 2 months
ABC is a 16-item questionnaire regarding confidence to perform different activities (e.g., walking around the house, up and down stairs, and on icy surfaces) without losing balance. The scale ranges from 0% (no confidence at all) to 100% (completely confident). An overall average balance confidence score will be calculated for each subject.
2 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Timed up and go test (TUG)
Time Frame: 2 months
The timed up and go test (TUG) is commonly used to assess functional mobility in older adults and is sensitive to fall risk (Shumway-Cook et al., 2000). The test involves standing up, walking as quickly and safely as possible for 3 m, turning around, walking back and then sitting down. Time to complete the TUG will be recorded.
2 months
Functional Gait Assessment (FGA)
Time Frame: 2 months
The 10 items of the FGA include walking while changing speed and turning the head, walking over obstacles, walking tandem, backward and with eyes closed and stair climbing. A maximum total score of 30 is possible with scores < 22 indicating high risk for falling (Wrisley et al., 2010).
2 months
Preferred gait speed
Time Frame: 2 months
Gait speed will be determined by instructing participants to walk at their normal pace over a 9-m pathway. The time to walk the middle 6 m will be measured using a stopwatch and gait speed calculated. Gait speed has excellent test-retest reliability (r = 0.90; Bohannon, 1997) and slower gait speed is associated with fall risk (Montero-Odasso et al., 2005).
2 months
Single Leg Stance Test
Time Frame: 2 months
The Single Leg Stance Test is a test of balance and requires participants to stand on one leg for up to 30 seconds. Up to three trials, using each leg will be performed. SLS is correlated with injurious falls (Vellas et al., 1997).
2 months
Modified clinical test of sensory interaction on balance (mCTSIB)
Time Frame: 2 months
The mCTSIB is organized into a series of 4 conditions of increasing difficulty and timed for a maximum of 30 seconds for each condition. The first two conditions involve a stable support surface with eyes open and eyes closed. The last two conditions involve a foam surface with eyes open and eyes closed. The mCTSIB score is the sum of the average time for each condition.
2 months
Physical Activity Scale for the Elderly (PASE)
Time Frame: 2 months
The PASE is comprised of self-reported occupational, household and leisure items over a one-week period and can be administered by telephone, mail or in-person.
2 months
Fear of Falling Avoidance Behavior Questionnaire
Time Frame: 2 months
The Fear of Falling Avoidance Behavior Questionnaire is a 14 item questionnaire that measures avoidance of behaviors due to fear of falling (Landers, Durand, Powell, Dibble, Young, 2011).
2 months

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Courtney Hall, PhD, East Tennessee State University

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)

August 1, 2016

Primary Completion (Actual)

December 31, 2017

Study Completion (Actual)

December 31, 2017

Study Registration Dates

First Submitted

October 27, 2016

First Submitted That Met QC Criteria

October 27, 2016

First Posted (Estimate)

October 31, 2016

Study Record Updates

Last Update Posted (Actual)

March 29, 2018

Last Update Submitted That Met QC Criteria

March 26, 2018

Last Verified

March 1, 2018

More Information

Terms related to this study

Other Study ID Numbers

  • ETSUIRB0716.5f

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

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.

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