The Effect Of A Resistance Exercise Program On Balance Of Elderly People

September 13, 2023 updated by: Kontonikas Konstantinos, University of West Attica

The Effect Of A Resistance Exercise Program On Balance Of Elderly People: A Pilot Trial

The purpose of the present study is to investigate the effectiveness of a resistance exercise program consisting of elastic band exercises to balance, strength and quality of life of community-dwelling elders. The hypothesis of the study is that the people training with elastic bands will show benefits on the aforementioned areas.

Study Overview

Status

Not yet recruiting

Conditions

Detailed Description

The elderly are, according to research, prone to an accelerated rate of loss of balance, particularly after the age of 60. This loss of balance could translate to injurious falls which could lead to trauma, fear of falling or even hospitalization. It has been shown in multiple studies that strength training can provide health benefits to the general population improving strength, balance, postural control, bone health and quality of life.

Elastic band exercises could be applied to a number of different settings due to the comparably low cost of equipment and due to the easiness of handling the equipment. In previous studies, elastic band exercise programs, varied in design, have been shown to provide multiple benefits to elderly people. In this study, it is proposed that in a Community Center for Elderly People, which are widely established in Greece, a group of eligible community dwelling elderly could exercise under supervision using elastic bands in a group setting.

The recruitment will take place in a Community Center for Elders. A group of people aged over 65, able and cleared to participate in strength training will participate. Information sheet and consent form will be provided to all participants. A pilot randomized intervention study is designed to assess the efficacy of elastic band resistance training as means to improve balance, strength and quality of life where the sample will be randomized to one of two following study groups:

  1. exercise program group (intervention group)
  2. no change of activities of daily living (control group)

Assessment will be obtained in two-time periods: prior to the program and after the program.

The exercise program will take place twice-weekly for eight weeks.

Participants will be assessed using Berg Balance Scale, Gait Speed, Timed Up and Go, 30 Seconds Chair Stand Test, Handgrip Strength, Knee Extensors and Flexors Strength, Fall Efficacy Scale.

Study Type

Interventional

Enrollment (Estimated)

20

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 Contact

Study Contact Backup

Study Locations

    • Attica
      • Athens, Attica, Greece
        • Elderly Community Center
        • Contact:
          • Kontonikas
        • Principal Investigator:
          • Kontonikas

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

  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Over 65 years old
  • Able to consent to participation
  • Able to stand without assistive devices
  • Able to participate in strength training
  • Able to perform activities of Daily Living independently
  • Cognitively and psychologically able to participate in a group setting

Exclusion Criteria:

  • Systematically exercised for up to 6 months prior to start of study
  • Neurological disorders or inability to stand
  • Recent surgery or contraindications to exercise
  • Arthroplasty or Prosthetic Limbs
  • Vision or Hearing problems hindering participation in group
  • Medication or Disorders contraindicating exercise or standing
  • Hypotension or Orthostatic Hypotension
  • Malignancy or Recent Treatment for Malignancy

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: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Exercise Program
Participants will participate in a group resistance exercise program for 8 weeks, using elastic bands.
8 Warm-Up Exercises followed by 10 Elastic Band Exercises followed by 8 Post-Workout Exercises.
No Intervention: Unchanged Activities of Daily Living
Participants will be asked not to change their activities of daily living for the duration of the research.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Berg Balance Scale
Time Frame: At baseline and after the end of the 8th week of the training program, at week number 9
The Berg Balance Scale (BBS) is used to objectively determine a patient's ability (or inability) to safely balance during a series of predetermined tasks. It is a 14 item list with each item consisting of a five-point ordinal scale ranging from 0 to 4, with 0 indicating the lowest level of function and 4 the highest level of function and takes approximately 20 minutes to complete. It does not include the assessment of gait.
At baseline and after the end of the 8th week of the training program, at week number 9

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Gait Speed 4 Meters
Time Frame: At baseline and after the end of the 8th week of the training program, at week number 9
The speed with which a patient walks for 4 meters. Gait speed is a metric that is extremely valuable for practitioners when examining aspects of functional mobility in their patients. Additionally, given its ability to be influenced by multiple body systems (i.e. central nervous system, musculoskeletal system), gait speed is often used as a predictor of overall health and function, especially in older adults.
At baseline and after the end of the 8th week of the training program, at week number 9
Timed Up and Go
Time Frame: At baseline and after the end of the 8th week of the training program, at week number 9
The patient is asked to stand from a sitting position, walk for three meters, turn around and return to seat. The purpose of this is to determine fall risk and measure the progress of balance, sit to stand and walking. It is a simple screening test that is a sensitive and specific measure of probability for falls among older adults.
At baseline and after the end of the 8th week of the training program, at week number 9
30 Seconds Chair Stand Test
Time Frame: At baseline and after the end of the 8th week of the training program, at week number 9
Patient is asked to alternate between sitting and standing for 30 seconds. The 30 second chair stand test is for testing leg strength and endurance in older adults.
At baseline and after the end of the 8th week of the training program, at week number 9
Handgrip Strength
Time Frame: Prior to the 1st week of the training program, After the end of the 8th week of the training program
Grip Strength is measured by use of a Grip Dynamometer. Grip strength is a measure of muscular strength or the maximum force/tension generated by one's forearm muscles. It can be used as a screening tool for the measurement of upper body strength and overall strength.
Prior to the 1st week of the training program, After the end of the 8th week of the training program
Lower Limb Strength (Flexors - Extensors of Knee)
Time Frame: At baseline and after the end of the 8th week of the training program, at week number 9
Muscle Strength will be measured by use of Dynamometer. An assessment of muscle strength is typically performed as part of a patient's objective assessment and is an important component of the physical exam that can reveal information about neurologic deficits. It is used to evaluate weakness and can be effective in differentiating true weakness from imbalance or poor endurance.
At baseline and after the end of the 8th week of the training program, at week number 9
Fall Efficacy Scale International (FES-I)
Time Frame: At baseline and after the end of the 8th week of the training program, at week number 9
The Falls Efficacy Scale International (FES-I) is a measure of "fear of falling" or "concerns about falling", developed as a part of the Prevention of Falls Network Europe (ProFaNE) project from 2003 to 2006 by Todd et al. It is a 16 item questionnaire, useful to the researchers and clinicians interested in fear of falling, with a score ranging from minimum 16 (no concern about falling) to maximum 64 (severe concern about falling). The FES-I is intended to be used in adult population to measure the level of concern about falling during social and physical activities inside and outside the home whether or not the person actually does the activity.
At baseline and after the end of the 8th week of the training program, at week number 9

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: K Kontonikas, University West Attica

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 (Estimated)

September 20, 2023

Primary Completion (Estimated)

November 30, 2023

Study Completion (Estimated)

December 1, 2023

Study Registration Dates

First Submitted

September 6, 2023

First Submitted That Met QC Criteria

September 13, 2023

First Posted (Actual)

September 15, 2023

Study Record Updates

Last Update Posted (Actual)

September 15, 2023

Last Update Submitted That Met QC Criteria

September 13, 2023

Last Verified

September 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • UWestAttica

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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