A Randomized Controlled Trial of the Effects of Reactive Neuromuscular Training on Balance

NCT00470938 | Completed Phase 1

• 1 other identifier: RD0202070062
• Study Type: interventional
• Target: N/A
• Locations: 0 countries
• Sites: N/A

Brief Summary

Falls are a major concern for the geriatric population and represent a significant public health problem. Various interventions are being explored to improve balance and decrease falls in the elderly. Success has been shown in some programs; various exercise interventions place emphasis on strength, balance, or endurance exercises. Results reported in the literature are still equivocal. Controversy exists as to optimal types of exercise, and the optimum frequency, duration, and intensity of exercise. It is believed that the SpineForce device, which places a unique combination of strength and balance demands upon the user, can result in rapid increases in balance as compared to other rehabilitation programs. Gains in balance have implications for geriatric populations as well as those seeking enhanced sports performance and injury prevention. The Purpose of this study is to assess the SpineForce device as a novel intervention in the treatment of balance disorders.

Conditions

Balance

Interventions

SpineForce Reactive Neuromuscular Trainer DEVICE

Eligibility Criteria

• Age: 20 Years - 30 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• Young, healthy adults between the ages of 20 - 30, asymptomatic with respect to any balance specific disorder, and who are currently enrolled at Logan College.

You may not qualify if:

• A previous lower extremity injury;
• Previous lower extremity surgery;
• A visual or vestibular condition with accompanying balance difficulty;
• A diagnosis of Knee osteoarthritis;
• Currently receiving spinal manipulative therapy;
• Current participation in a regular exercise program;
• Use of any prescription medication, or herbal substance that may affect balance;
• Pregnancy

Sponsors & Collaborators

• Logan College of Chiropractic: lead

Study Officials

• Rodger Tepe, PhD

  Logan College of Chiropractic

  STUDY DIRECTOR

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: RANDOMIZED
• Masking: NONE
• Intervention Model: PARALLEL
• Sponsor Type: OTHER

Study Record Dates

• First Submitted: May 4, 2007
• First Posted: May 8, 2007
• Study Start: March 1, 2007
• Primary Completion: March 1, 2007
• Study Completion: March 1, 2007
• Last Updated: February 29, 2008

Record last verified: 2008-02