Motor Imagery Training in Community Dwelling Elderly

September 1, 2021 updated by: Imtiyaz Ali Mir, Universiti Tunku Abdul Rahman

Effect of Motor Imagery Training On Quadriceps Strength In Community Dwelling Elderly

An aging society is known as having at least 7% of its population aged 65 and older, whereas 14% or more known to be an aged nation. Age has a detrimental effect on the physical performance and the muscle strength, the reduced muscle strength, mass and structure in the elderly are due to aging, disuse and inactivity. In the elderly, the reduction of muscle strength is faster than the associated loss of muscle mass. The maximum isometric strength of knee extensors and muscle mass decrease due to aging. The combination of quadriceps and handgrip strength weakness in the elderly is associated with the poorest scores on quality of life, GP contact-time, gait speed, hospitalization and disability in daily living. Quadriceps weakness among elderly is also proved to be a contributing factor to fall among frail nursing home residents. A systematic review and meta-analysis revealed that quadriceps muscle weakness was associated with greater risk of developing knee osteoarthritis during 2.5 to 14 year follow-up in either gender. In overall, aging cause reduce muscle strength, especially quadriceps muscle, can cause many others negative consequences, thus a study of effect motor imagery on quadriceps muscle strength in community-dwelling elderly should be carried out, if this study is proven to effectively, motor imagery technique can be widely utilized on bedridden elderly or elderly who have severe cardiovascular disease who unable to perform physical activity to maintain or improve their muscle strength.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Detailed Description

The decrease in the number of skeletal muscle and decline in muscle function is the most important factor in influencing the ability to perform physical function independently in the later stage of our life. The reduction of quadriceps strength with advancing age in both gender is proved to be associated with an increased risk of fractures, increased chance of worsening of knee pain, high risk of osteoarthritis. Quadriceps weakness is also proved to be a contributing factor to falls among frail nursing home residents.

Motor imagery had been widely utilized and proved to benefits different population. Motor imagery training makes a better motor performance as proved to be an effective tool in stroke rehabilitation, it is effective and useful when there are severely injured patients. This imagery training has turned into performance enrichment ways and simulation tools which has been widely utilized in sports psychological interventions as well.

Motor imagery can be defined as a dynamic mental state during which the representation of a given motor act or movement is rehearsed in working memory without any overt motor output. Motor imagery can also be defined as utilizing whole senses to reform or form an experience in one's thought. Motor imagery can be performed in different modes which can be classified into visual, tactile, auditory, gustatory, olfactory, and kinesthetic modes. There are lot of studies which have showed that motor imagery task does activate the cortical and subcortical regions of the brain and they overlap in a great extent with task required movement execution. The parts of the brain proved to participate in motor control consists of the premotor cortex (PMC), supplementary motor area (SMA), as well as the primary motor cortex (M1). All these brain areas are nearly related to the basal ganglia and cerebellum, as a result, large feedback loop systems are formed. The aim of this research is to investigate the effect of motor imagery training on quadriceps strength among community-dwelling elderly. The second aim of our study is to compare the gender differences with regards to quadriceps muscle improvement after motor imagery training.

Study Type

Interventional

Enrollment (Anticipated)

50

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

    • Selangor
      • Kajang, Selangor, Malaysia, 43000
        • Recruiting
        • Universiti Tunku Abdul Rahman
        • Contact:
        • Sub-Investigator:
          • Chong Zheng Wei
        • Sub-Investigator:
          • Mohammed Abdulrazzaq Jabbar

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

60 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Both gender
  • Aged 60 and above
  • Participant who has a mean score of more than 3 in Movement Imagery Questionnaire-3
  • Participant who scored 22 and above in MONTREAL COGNITIVE ASSESSMENT (MOCA) VERSION 7.1

Exclusion Criteria:

  • Individual with neurological impairment or musculoskeletal injury.
  • Participants unable to follow the instructions.
  • Individuals using any anti-epileptic drugs and/or psychiatric drugs.

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: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Control
No intervention provided.
Experimental: Motor Imagery
The participants were instructed to imagine and visualize to straighten both knees with eyes closed. You have to see and feel only what you would see and feel if you had to perform the action to straighten both of your knees in sitting position. Imagine the movement using the most comfortable way for you, and make sure not to contract your muscles.
The number of imagined contractions were 34 trials, each trial was 10 seconds with 5seconds rest between each trial and 2 minutes' rest was given after first 17 trials.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Quadriceps Strength
Time Frame: Change from baseline Quadriceps strength at 4 weeks
The participants were in sitting position, hand-held dynamometer was place on the shin of the tibia just above medial and lateral malleolus. Before measuring the quadriceps strength, participant's knees were held in 90-degree flexion and feet not in contact with the floor. The participants were instructed to straighten leg by pushing against hand-held dynamometer. Peak force generated by dynamometer was recorded. The measurement was repeated three times to take an average of 3.
Change from baseline Quadriceps strength at 4 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this 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 (Actual)

August 8, 2021

Primary Completion (Anticipated)

February 10, 2022

Study Completion (Anticipated)

February 10, 2022

Study Registration Dates

First Submitted

June 2, 2021

First Submitted That Met QC Criteria

June 2, 2021

First Posted (Actual)

June 9, 2021

Study Record Updates

Last Update Posted (Actual)

September 2, 2021

Last Update Submitted That Met QC Criteria

September 1, 2021

Last Verified

September 1, 2021

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • UMFD3026-4

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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