Noise-Enhanced Sensory Function in Elders at Risk for Falls

December 10, 2009 updated by: National Institute on Aging (NIA)
The long-term goal of this project is to develop a non-invasive, noise-based technique for enhancing somatosensation and thereby improving balance control in elderly fallers and older adults with somatosensory deficits.

Study Overview

Status

Unknown

Intervention / Treatment

Detailed Description

Previous studies have shown that sub-sensory mechanical noise (i.e., random vibration with a small intensity) can enhance somatosensory function in healthy individuals and older adults with somatosensory deficits. Moreover, the postural sway of both healthy young and healthy elderly individuals during quiet standing can be significantly reduced by applying sub-sensory mechanical noise to the feet using vibrating shoe insoles.

The specific aims of this project are to determine the effects of noise-enhanced somatosensation at the feet on balance performance in elderly individuals with somatosensory deficits and/or recurrent falls, and to assess whether adaptation occurs in noise-enhanced balance control in these individuals. To accomplish these aims, quiet-standing and dynamic posture studies and clinical balance assessments will be conducted on elderly individuals with somatosensory deficits and elderly individuals with recurrent falls (two or more falls over a 12-month period).

This project could lead to the development of a novel bioengineering technique for improving balance control in older adults and patients with somatosensory deficits. The work could thus serve to reduce the frequency, morbidity and cost of falling, and assist aged individuals in achieving maximal independence in activities of daily living and mobility.

Two groups of participants will be recruited from the RNH Epidemiology Core: 85 elderly individuals with somatosensory deficits, and 85 elderly individuals with recurrent falls. The study consists of three visits--a one-hour neurological exam, and two 6-hour laboratory testing sessions scheduled one week apart.

Study Type

Interventional

Enrollment (Anticipated)

170

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

    • Massachusetts
      • Boston, Massachusetts, United States, 02215
        • Recruiting
        • Applied Biodynamics Laboratory, Boston University
        • Contact:
        • Principal Investigator:
          • James Collins, MD

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

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Participant must (1) have somatosensory deficit (mild to moderate sensory loss on the bottom of both feet) OR (2) be classified as a recurrent faller (two or more incident falls over a twelve-month period not related to syncope, major medical events, or overwhelming external hazards)
  • Age 70 and older
  • Able to stand unassisted for at least 60 seconds several times over a 30-minute period
  • Able to walk without assistance from a walking aid

Exclusion Criteria:

  • Known history of seizures or fainting
  • Unstable medical condition
  • Open lesions or poor skin condition on feet
  • Unable to cooperate with or understand the protocol
  • Foot size larger or smaller than the constructed vibrating insoles (men's sizes smaller than 3 or larger than 12; women's sizes smaller than 4.5 or larger than 13.5)

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: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: Quadruple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: 1
85 elderly individuals with somatosensory deficits
Participants wear vibrating sandals for 3 trials of 6 minutes, during a single lab visit. The sandal vibration is on during either first or second 3 minutes of the 6 minute trial, as they walk. Also, participants wear the sandals for 2 hours while sitting, with vibrations on for one visit and off for the other.
Experimental: 2
85 elderly individuals with recurrent falls
Participants wear vibrating sandals for 3 trials of 6 minutes, during a single lab visit. The sandal vibration is on during either first or second 3 minutes of the 6 minute trial, as they walk. Also, participants wear the sandals for 2 hours while sitting, with vibrations on for one visit and off for the other.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Area ellipse of sway
Time Frame: Three 6-minute trials in one visit, repeated one week later
Three 6-minute trials in one visit, repeated one week later
Berg Functional Balance Scales
Time Frame: Three 6-minute trials in one visit, repeated one week later
Three 6-minute trials in one visit, repeated one week later
Timed Up and Go (TUG)Test
Time Frame: Three 6-minute trials in one visit, repeated one week later
Three 6-minute trials in one visit, repeated one week later
Timed one-legged stance test
Time Frame: Three 6-minute trials in one visit, repeated one week later
Three 6-minute trials in one visit, repeated one week later
Gait timing variability
Time Frame: Three 6-minute trials in one visit, repeated one week later
Three 6-minute trials in one visit, repeated one week later

Secondary Outcome Measures

Outcome Measure
Time Frame
Changes in: stabilogram-diffusion analysis (SDA)
Time Frame: Three 6-minute trials in one visit, repeated one week later
Three 6-minute trials in one visit, repeated one week later
Neurological risk factors related to falls
Time Frame: Three 6-minute trials in one visit, repeated one week later
Three 6-minute trials in one visit, repeated one week later

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

April 1, 2006

Primary Completion (Anticipated)

January 1, 2009

Study Completion (Anticipated)

January 1, 2009

Study Registration Dates

First Submitted

January 10, 2007

First Submitted That Met QC Criteria

January 10, 2007

First Posted (Estimate)

January 12, 2007

Study Record Updates

Last Update Posted (Estimate)

December 14, 2009

Last Update Submitted That Met QC Criteria

December 10, 2009

Last Verified

August 1, 2008

More Information

Terms related to this study

Other Study ID Numbers

  • AG0072
  • 5P01AG004390-230014
  • 5P01AG004390 (U.S. NIH Grant/Contract)

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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