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Variability of Movement on an Altered Inertial Dynamics Task

Not Applicable
Completed
Conditions
Older Adults
Fall Patients
Interventions
Behavioral: Forward walking
Behavioral: Lateral stepping
Registration Number
NCT04505527
Lead Sponsor
University of Nebraska
Brief Summary

The overall goal of this research is to compare the effects of two different exercise programs on gait function in older adults. The investigators want to determine if participation in lateral stepping exercise program for six weeks will improve gait functions compared to forward walking exercise program.

Detailed Description

The overall goal of this research is to compare the effects of two different exercise programs on gait function in older adults. It is expected that improved control of foot placement in the lateral stepping task will transfer to improved control during typical forward walking. Moreover, it is expected that lateral stepping gait training will have a greater effect on recurrent fallers older adults than on the non-fallers older adults and young adults. It is also expected that the above beneficial results will be retained in a follow-up test six weeks after completion of the intervention and will result in improvements in common clinical balance tests that are used to assess fall risk. Therefore, in the current proposal, older adults aged 65 years of age and over are being asked to participate.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
15
Inclusion Criteria

Subjects must

  • be aged between 19 and 35 for the young adult group
  • be over 65 years of age for the older adult groups
  • be independently residing in the community
  • be able to provide informed consent
  • be able to walk independently without an assistive device or 30 minutes in three-minute sections interspersed with rest periods.

The older participants must either have sustained two or more falls in the past year (i.e. Fallers) or not have sustained any falls in the past year (i.e. Non-Fallers).

Exclusion Criteria
  • Neurological disorder or progressive neurologic condition - epilepsy, Alzheimer disease and other dementias, stroke, multiple sclerosis, Parkinson's disease, brain infections, brain tumors.
  • Movement disorder - ataxia, dystonia, Huntington's disease, myoclonus, Parkinson disease, progressive supranuclear palsy, Wilson disease.
  • History of Cardiovascular events this includes any history of heart problems (such as heart attack, chest pain, or conditions which affect the heart's muscles, valves, or rhythm)
  • Current injury or moderate to severe pain affecting the lower limbs, pelvis, back, trunk.
  • Surgery within the past 6 months.
  • Current participation in any other study that involves walking, balance, or training.

Medications will not prevent inclusion in the study however they will be recorded to enable consideration in subsequent post-hoc analyses.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Recurrent fallers - control groupForward walkingIn this control arm, older adults will have a typical forward walking training that mirror the lateral stepping intervention: 3 days/week for 6 weeks, resulting in a total of eighteen sessions. Each session consists of six trials of 3 min forward walking. The participants can increase their pace at the start of each trial but may not decrease it at the next session.
Older non-fallers intervention groupLateral steppingIn this experimental arm, older adults will have a lateral stepping intervention: 3 days/week for 6 weeks, resulting in a total of eighteen sessions. Each session consists of six trials of 3 min sideways walking across a 10 m walkway changing body direction at the ends, thus alternating lead and lag limbs. The participants can increase their pace at the start of each trial but may not decrease it at the next session.
Recurrent fallers - intervention groupLateral steppingIn this experimental arm, older adults will have a lateral stepping intervention: 3 days/week for 6 weeks, resulting in a total of eighteen sessions. Each session consists of six trials of 3 min sideways walking across a 10 m walkway changing body direction at the ends, thus alternating lead and lag limbs. The participants can increase their pace at the start of each trial but may not decrease it at the next session.
Younger adult control groupLateral steppingOutcome measures from a young healthy group will also be measured as a reference. Will be used to compare outcome measured between older and young adults. Young adults will have a lateral stepping intervention: 3 days/week for 6 weeks, resulting in a total of eighteen sessions. Each session consists of six trials of 3 min sideways walking across a 10 m walkway changing body direction at the ends, thus alternating lead and lag limbs. The participants can increase their pace at the start of each trial but may not decrease it at the next session.
Primary Outcome Measures
NameTimeMethod
Swing time variabilityBaseline and Post-Intervention: immediate, and 6 weeks after the completion of the intervention

The standard deviation of swing time. Swing time was measured as the time elapse during the swing phase of a leg.

Stance time variabilityBaseline and Post-Intervention: immediate, and 6 weeks after the completion of the intervention

The standard deviation of stance time. Stance time was measured as the time elapse during the stance phase of a leg.

Timed-Up-and-Go (TUG)Baseline and Post-Intervention: immediate, and 6 weeks after the completion of the intervention

The Timed-Up-and-Go test is used to assess mobility in older adults. It measures the time to get up from chair, walk 3 m, turn around, walk back, and sit down

Berg Balance Test (BBS)Baseline and Post-Intervention: immediate, and 6 weeks after the completion of the intervention

The Berg Balance Test (14 items, max score: 56) is used to measure the functional balance in older adults. It consists of 14 tasks performed in a standardized order with each task scored on a five-point scale according to quality or time ranging from "0" (lowest level of function) to "4" (highest level).

Step length variabilityBaseline and Post-Intervention: immediate, and 6 weeks after the completion of the intervention

The standard deviation of step length. Step length was measured as the anteroposterior distance between the locations of the sequential left and right heel strikes.

Stride time variabilityBaseline and Post-Intervention: immediate, and 6 weeks after the completion of the intervention

The standard deviation of stride time. Stride time was measured as the time between 2 consecutive ipsilateral heel strikes.

Step width variabilityBaseline and Post-Intervention: immediate, and 6 weeks after the completion of the intervention

The standard deviation of step width. Step width was measured as the mediolateral distance between the locations of the sequential left and right heel strikes

Secondary Outcome Measures
NameTimeMethod
Walking speedBaseline and Post-Intervention: immediate, and 6 weeks after the completion of the intervention

Self-selected forward walking and sideways walking speed

Falls Efficacy Scale-International (FES-I)Baseline and Post-Intervention: immediate, and 6 weeks after the completion of the intervention

The Falls Efficacy Scale-International (FES-I) questionnaire (16 items, max score: 64) is used to assess confidence in the performance of activities relevant to daily life. Participants rate 16 individual activities on a scale from 1 (not at all concerned) to 4 (very concerned).

Trial Locations

Locations (1)

University of Nebraska-Omaha, Biomechanics Research Building

🇺🇸

Omaha, Nebraska, United States

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