- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04969094
Reducing Fall Risk With NMES (NMES)
Reducing Fall Risk With the Use of Neuromuscular Electrical Stimulation to Maximize the Hip Abductor Muscles in Older Veterans
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Falls are a leading cause of disability in older adults. Decreased lower extremity muscle mass and strength contribute to balance and mobility limitations. More recent work also suggests that in addition to the traditional targets of muscle mass of the thigh and leg muscles, dysfunction of the hip abductors may contribute to balance and mobility limitations resulting in increased fall risk. Older adults with impaired hip abductor muscles demonstrate increased amounts of intramuscular fat (IMAT) in and around the muscles, decreased hip abductor strength, lower balance scores, increased gait variability (a predictor of future falls), and poor stepping mechanics when recovering from a balance perturbation. Increased IMAT and muscle dysfunction of the hip abductors may contribute to poor hip abductor muscle recruitment and make changing these muscle during a traditional intervention difficult. Neuromuscular electrical stimulation (NMES) is one method to improve muscle mass, strength and quality in older adults, but has not traditionally been used on the hip abductors. The investigator's central hypothesis is that the addition of NMES applied to the primary hip abductors during a multimodality balance intervention (MMBI) will result in greater reduction in fall risk and larger improvements in muscle and mobility function than MMBI alone. The investigators will test this hypothesis with the following specific aims:
Aim 1: To determine the 3-month effects of a multimodality balance intervention with and without NMES on fall risk.
Aim 2: To examine the 3-month effects of a multimodality balance intervention with and without NMES on functional outcomes including muscle function and composition.
Aim 3: To evaluate the retention of balance, muscle changes and reduced falls after a multimodality balance intervention with and without NMES
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Maryland
-
Baltimore, Maryland, United States, 21201
- Baltimore VA Medical Center VA Maryland Health Care System, Baltimore, MD
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- 55 years or older
- At risk for falls
Exclusion Criteria:
- Poorly controlled hypertension
- Home oxygen use
- Contraindications to resistance exercise
- Contraindications for NMES use
- Dementia
- Other medical condition precluding patient participation in this study as per medical judgment of study team
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: NMES + MMBI
Neuromuscular electrical stimulation applied to hip abductors along with participation in a multi-modality balance intervention
|
Participants will receive NMES to the hip abductors while performing strength training 3 times per week for 3-months
Participants will attend a group balance class that focuses on movement and obstacle negotiation 3 times per week for 3-months
|
|
Active Comparator: MMBI
Participation in a multi-modality balance intervention
|
Participants will attend a group balance class that focuses on movement and obstacle negotiation 3 times per week for 3-months
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Balance
Time Frame: 3-months
|
The four-square step test will be used as a measure of balance.
The change in the amount of time it takes to complete the four-square step test comparing pre and post-intervention.
|
3-months
|
|
Isometric Hip Abductor Strength
Time Frame: 3-months
|
A measure of the maximal isometric muscle strength produced in hip abductor muscles will be assessed with a biodex device.
Pre-test levels will be compared to post-intervention levels.
|
3-months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Mobility
Time Frame: 3-months
|
The modified physical performance test is a mobility measure that utilizes 9 tasks scored 0-4 (total possible score 36) to determine functional status.
Pre-test scores will be compared to post intervention test scores.
|
3-months
|
|
Muscle composition
Time Frame: 3-months
|
A measure of the amount of muscle and fat in the muscle using a CT scan of the hips.
Pre-test levels will be compared to post intervention levels
|
3-months
|
|
Balance
Time Frame: 12-months after Exercise completion
|
The change in the amount of time it takes to complete the four-square step test comparing post-intervention to 12-months after the cessation of exercise.
|
12-months after Exercise completion
|
|
Isometric Hip Abductor Strength
Time Frame: 12-months after Exercise completion
|
A measure of the maximal isometric muscle strength produced in hip abductor muscles will be assessed with a biodex device.. Post-intervention levels will be compared to 12 months after the cessation of exercise.
|
12-months after Exercise completion
|
Collaborators and Investigators
Investigators
- Principal Investigator: Odessa R. Addison, PhD DPT, Baltimore VA Medical Center VA Maryland Health Care System, Baltimore, MD
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- E3484-R
- RX003484 (Other Grant/Funding Number: Veteran Affairs Rehabilitation R&D Service)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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.
Clinical Trials on Falls
-
National University, SingaporeRecruitingFalls Prevention | Falls RiskSingapore
-
The Hospital District of SatakuntaCompleted
-
Aga Khan UniversityFogarty International Center of the National Institute of HealthActive, not recruitingFalls Injury | Falls | Accidental Falls | Mobility Difficulty | Mobility and Independence | Aged 60 Years or OlderPakistan
-
University Hospital, Basel, SwitzerlandCompletedAccidental Falls | Underlying Disease of FallsSwitzerland, Germany
-
Peking UniversityActive, not recruitingFalls Injury | Falls | Fall PreventionChina
-
Brigham and Women's HospitalNational Institutes of Health (NIH); National Institute on Aging (NIA)CompletedFall Injury | Falls | Exercise Self-Efficacy | Falls Self-EfficacyUnited States
-
VA Office of Research and DevelopmentNot yet recruiting
-
Brookside Research & Development CompanyNational Institute on Aging (NIA)Active, not recruiting
-
University of British ColumbiaCanadian Institutes of Health Research (CIHR)Completed
-
University of British ColumbiaWithdrawn
Clinical Trials on Neuromuscular electrical stimulation (NMES)
-
Hopital ForcillesNot yet recruitingDysphagia | NeuroMuscular Electrical Stimulation
-
Karolinska University HospitalDanderyd HospitalNot yet recruitingMuscle Atrophy | Venous Thromboembolism (VTE) | Immobilization | Achilles Tendon Ruptures
-
Federal University of Health Science of Porto AlegreRecruitingAnterior Cruciate Ligament Reconstruction | Anterior Cruciate Ligament Reconstruction RehabilitationBrazil
-
Aslinur Keles Ercisli, MD, PhDFatih Sultan Mehmet Training and Research HospitalNot yet recruitingCerebral Palsy (CP) | DroolingTurkey (Türkiye)
-
Federal University of Rio Grande do SulTerminated
-
Vastra Gotaland RegionGöteborg UniversityRecruitingPhysical Disability | Achilles Tendon RuptureSweden
-
Research Institute for Complex Problems of Cardiovascular...UnknownSarcopenia | Heart Failure, SystolicRussian Federation
-
University of VermontNational Institute on Aging (NIA)CompletedKnee OsteoarthristisUnited States
-
Research Institute for Complex Problems of Cardiovascular...UnknownHeart Failure | Sarcopenia | Peripheral Artery Disease | Exercise IntoleranceRussian Federation
-
Escola Superior de Ciencias da SaudeRecruitingCovid19 | Muscle Weakness Condition | Mechanical Ventilation ComplicationBrazil