Perturbation Training to Improve Balance Recovery of Old Adults (BalancING)

April 17, 2024 updated by: Soroka University Medical Center

The Influence of a Perturbation Training on Balance Recovery of Old Adults - a Randomized Controlled Trial

Falls are major contributors for immobility and independency. Most falls in older adults occur during walking after a sudden unexpected loss of balance. It was well-established that balance can be improved by performance of a training program that provides perturbation (unexpected perturbations of balance). The main aim of the current study is to investigate the effects of two perturbation-training methods: 1) random perturbation training; vs. 2) block (non-random) perturbation training. We also aim to explore brain area's (as measured by MRI) that are related to balance function in older adults.

We hypothesize that response to an unexpected loss of balance is the balance responses will be improved in both training methods, but more in the random training method. We also hypothesize that brain function as seen in MRI will be improved in both training methods, more in the random training method.

As far as we know, there is a lack of studies investigating the learning effect of random vs. block non-random training on balance recovery responses while walking and exposure to unexpected loss of balance and on brain function.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Goals:

  1. Determine the relationship between gait stability (as measured in the Lab) and brain function (MRI) in 50 old (70 years old and over) and 10 young adults (20-40 years old) that represent heathy brain.
  2. To determine which of the training intervention methods (25 older adults that participate in random training vs. 25 older adults that participate in block non-random training) are more beneficial for balance recovery responses and for improved brain function.

Methods: This study is a clinical investigation study. First stage - Individuals that show an interest in participating in the study will be exposed to a brief interview before further testing is performed to see if they fit the inclusion-exclusion criteria. Individuals who pass the interview a screening, and physical examination and the additional questionnaires and functional tests described below.

Second stage - Testing different motor learning paradigms for improving balance recovery ability: A convenience sample of 60 healthy subjects (10 young's, 50 older adults) will be recruited. After testing their clinical balance performance (Berg balance test, 6-minutes' walk and get up and go) and cognitive function (MOCA), All testing will occur on a specific motor-driven surface perturbation treadmill (BaMPer). The Gait protocol will include about 10-20 minutes of comfortable pace walking, than progressive unexpected surface perturbations will be added. The same protocol will be performed with during standing condition. Subjects will also walk on the treadmill without perturbations. The order of the different test conditions will be randomized.

Outcome measures: The stepping threshold as measured by the distance of the platform movements in centimeters will be measured. Quantitative parameters of the compensatory stepping/ and motor ability (i.e., step reaction time, step time, step length), descriptive parameters of the stepping strategy after perturbation

(i.e., arm responses, upper body responses, leg step threshold and fall threshold). In addition, we will be testing the correlation between brain activity and anatomy using brain imaging in 10 young and 50 older adults and correlate with balance/motor function.

The aims of this study are to determine the relationship between the different requirements for gait stability (walking without perturbations, ability to overcome small perturbations, ability to overcome larger perturbations and, largest recoverable perturbation during walking) and brain function and anatomy. The research hypothesis: there is a correlation between the age related atrophies in areas of the brain and functional capacity

Third stage - A Randomized control trial we will compare two perturbation motor learning paradigms with different challenge level of the practice condition (i.e. blocked practice vs random practice). According to motor learning theory we hypothesize that a) healthy older adults will benefit more from random practice. The purpose of this stage is to investigate the effects of task practice order (random vs blocked) on motor learning (i.e. responding to perturbations during walking) in older adults. According to motor learning theory we hypothesize that a) healthy older adults will benefit more from the random motor learning approach as compared to using blocked practice.

Study Type

Interventional

Enrollment (Actual)

25

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 Contact

Study Contact Backup

  • Name: Itshak Melzer, PhD
  • Phone Number: 972-8-6477725

Study Locations

      • Beer-Sheva, Israel, 84105
        • Ben-guion University of the Negev,
      • Beer-Sheva, Israel, 84105
        • SorokaUMC
      • Beer-Sheva, Israel, 84105
        • Soroka Medical Center

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 to 120 years (Older Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  1. 70 years and older (with the young age of 20-40)
  2. able to walk independently (without utilities treadmill or stick);
  3. Be asked to invent a medical certificate which allows participation in exercise that requires walking twice a week.

Exclusion Criteria:

  1. suffering from ischaemic heart disease which limits exercise and COPD and blood pressure is not controlled;
  2. not suffering serious vision problems;
  3. does not suffer from this problem: (a score of 24 or higher on MOCA);
  4. a year after analyzing the type of hip replacement or knee or broken extremities;
  5. Does not suffer any neurological diseases or stroke.

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: experimental group
Random perturbation training
A Randomized control trial we will compare two perturbation motor learning paradigms with different challenge level of the practice condition (i.e. blocked practice vs random practice). According to motor learning theory we hypothesize that a) healthy older adults will benefit more from random practice. The purpose of this stage is to investigate the effects of task practice order (random vs blocked) on motor learning (i.e. responding to perturbations during walking) in older adults. According to motor learning theory we hypothesize that a) healthy older adults will benefit more from the random motor learning approach as compared to using blocked practice.
Active Comparator: control group
Block perturbation training
A Randomized control trial we will compare two perturbation motor learning paradigms with different challenge level of the practice condition (i.e. blocked practice vs random practice). According to motor learning theory we hypothesize that a) healthy older adults will benefit more from random practice. The purpose of this stage is to investigate the effects of task practice order (random vs blocked) on motor learning (i.e. responding to perturbations during walking) in older adults. According to motor learning theory we hypothesize that a) healthy older adults will benefit more from the random motor learning approach as compared to using blocked practice.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The step recovery thresholds and brain imaging (MRI)
Time Frame: 60 minute
The stepping threshold as measured by the distance of the platform movements in centimeters will be measured. Quantitative parameters of the compensatory stepping/ and motor ability (i.e., step reaction time, step time, step length), descriptive parameters of the stepping strategy after perturbation (i.e., arm responses, upper body responses, leg step threshold and fall threshold). In addition we will be testing the correlation between brain activity using brain imaging in both to find whether improvement in motor function are correlated with brain function and anatomy.
60 minute

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Postural stability
Time Frame: 10 minutes
participants will be instructed to stand upright on the force platform with the feet positioned as close as possible (heels and toes touching). A total of six 30-second trials will conduct for two visual conditions: eyes open and eyes closed. Balance measurements will be collected with a Kistler 9287 single force platform (Kistler Instrument Corp, Winterthur, Switzerland), which measures the time-varying displacement of the center of pressure (CoP) under the participant's feet. The force platform data will be sampled at a frequency of 100 Hz and stored on a hard disk for later processing.
10 minutes
Voluntary step test
Time Frame: 6 minutes
subjects will be instructed to step as quickly as possible following a cue signal
6 minutes
Berg Balance test
Time Frame: 10 minutes
The participant is scored on 14 balance tasks. Maximum score of 56 represents good balance. Higher scores indicate higher levels of balance function, while 45 or less indicates a high risk of falling.
10 minutes
kinematics of walking
Time Frame: 10 minutes
subjects will be instructed to walk on a treadmill. During the experiment we will measure by 3D motion analysis system gait kinematics during walking at their preferred speed for 2 minutes.
10 minutes

Collaborators and Investigators

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

Investigators

  • Study Chair: ilan Shelef, MD, Soroka University Medical Center

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 (Actual)

October 1, 2017

Primary Completion (Actual)

December 31, 2021

Study Completion (Actual)

December 31, 2021

Study Registration Dates

First Submitted

June 29, 2020

First Submitted That Met QC Criteria

June 29, 2020

First Posted (Actual)

July 2, 2020

Study Record Updates

Last Update Posted (Actual)

April 18, 2024

Last Update Submitted That Met QC Criteria

April 17, 2024

Last Verified

October 1, 2020

More Information

Terms related to this study

Other Study ID Numbers

  • Sor 396-16 CTIL

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.

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