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Effect of Perturbation Training on Balance Control in Elderly Persons

Effect of Balance Perturbation to Improve Gait and Balance Control and Prevent Falls in Elderly Persons -A Randomized Control Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01439451
Acronym
BaMPer
Enrollment
48
Registered
2011-09-23
Start date
2011-08-31
Completion date
2015-08-31
Last updated
2015-08-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Accidental Falls

Keywords

Balance control, Aging, Balance reactions, Perturbation, above seventy years old

Brief summary

The proposed project is a prospective experimental Randomized Control Trial study design. Independent old adults (age 70 years old and older) who do not suffer from balance problems willing to participate in the study will be tested before and after Peturbation balance training during walking to explore whether there are differences in balance control and balance reactions as a result of training.

Detailed description

A total of 48 old adults will be enrolled, evaluated and trained. They will be randomly assigned to two groups: one exercise group (perturbation training) and one group without perturbation. No gender based differences are expected for the recovery outcome measures so we will be able to pool male and female individuals for this analysis. Each subject of the experimental and of the control groups will be trained on 24 occasions over a period of 10-12 weeks (20-30 minutes, 2-3 times/week). This regimen was based on previous balance training study that demonstrated improvements in balance control with similar training duration and frequency. Gait and balance function and physical activity level will be tested in both groups before, immediately after, 3 and 6 months after completion of the training period to explore the benefit and carryover of training. In addition using monthly phone calls, falls, their severity, functional activity limitations in the home and community setting and health status will be monitored 12 months after the training period.

Interventions

The experimental and control groups will participate in 3 month training program twice a week 20 minutes each training session

Sponsors

Barzilai Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
70 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Be 70 years or older, male or female * Be an independent ambulator (not cane or walker) and provide medical waiver from MD.

Exclusion criteria

* Severe focal muscle weakness or paralysis, after Total Hip or knee arthroplasty * Moderate-severe dementia (Mini-Mental Score \< 24). * Serious visual impairment * Severe peripheral or compression/entrapment neuropathies. * Symptomatic orthostatic hypotension, respiratory, cardiovascular, musculoskeletal, or neurological disorders that may interfere with participation in the exercise program. * Cancer, metastatic or under active treatment.

Design outcomes

Primary

MeasureTime frameDescription
voluntary and compensatory step execution times in milisecondschange from baseline to 3 months laterthe time from perturbation to foot contact the floor completing the recovary stepping will be measured in miliseconds

Secondary

MeasureTime frameDescription
postural sway parameters such as mediolateral sway in milimeters and elliptical area in milimeters squeresTime 1: pre test' and 3 months later time 2: post testing procedurebody sway will be measured to evaluate control of posture

Countries

Israel

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 2, 2026