Skip to main content
OpenTrials
Recruiting

NCT Number: NCT07405060

Impacts and Mechanisms of Age and Muscle Fatigue on Postural Control and Force Control

Muscle fatigue is one of the clinical symptoms in elderly people and demonstrates task dependency and muscle dependency. Muscle fatigue has been shown to negatively impact postural control, physical activity, and quality of life. However, the evidence for the influence of muscle fatigue on postural control is limited and inconsistent in elderly people. Therefore, this study aims to investigate the impacts of aging and muscle fatigue on postural control and gait performance with fatiguing exercises of upper and lower extremities.

Recruiting

Interested in participating?

Request Info

Key information

Conditions

Age range

20 year–85 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Chang Gung Memorial Hospital, Taoyuan, Taiwan

Loading trial locations.

About this study

This study aims to investigate the effects of muscle fatigue on postural control and gait performance in healthy older adults (≥65 years) and young adults (20-40 years). Neuromuscular fatigue has been associated with postural instability, but its influence on gait and potential age-related differences remain unclear. Therefore, this study will compare fatigue-induced changes in motor performance between age groups and examine whether fatigue of the upper and lower extremities produces similar functional effects.

Healthy older adults and young adults will be recruited from the community. Eligible participants must be in good health, able to walk independently, demonstrate normal cognitive function, and provide informed consent. Individuals with neurological, cardiovascular, musculoskeletal, or other conditions that may affect motor performance will be excluded.

A repeated-measures design will be used. The study will involve two laboratory sessions separated by at least one week. Participants will undergo pre-test assessments, a fatiguing exercise protocol, and post-test assessments. Motor outcomes-including maximal voluntary isometric contraction, postural control, and gait performance-will be measured before and after the fatiguing exercises. Fatiguing exercises will consist of repeated cycles of maximal contractions with rest periods, while heart rate and perceived exertion are monitored to ensure safety. The protocol will terminate if exertion reaches a predefined threshold or heart rate exceeds the age-predicted maximum.

Surface electromyography and electrical stimulation will be used to assess neuromuscular function. Postural control will be evaluated using a force plate under multiple standing conditions, and gait parameters will be measured while participants walk at comfortable and fast speeds. Statistical analyses will use repeated-measures mixed-model ANOVAs to examine the effects of age group and fatigue on motor outcomes.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 20 to 40 years (young), and 60-85 years (old)
  • walk independently
  • able to follow commands (Mini Mental Status Exam (MMSE) scores greater than 21
  • able and willing to provide informed consent.

Exclusion criteria

  • pregnancy
  • neurologic, psychiatric, cardiac, vascular, pulmonary, musculoskeletal, immune, integumentary disease or disorder which might influence this study
  • any current loss of sensation in the arms, wrists, hands, fingers, hips, knees, ankles or toes
  • any pain at the time of testing
  • any restriction in range of motion of lower extremity.

Treatment and study plan

age

Other

We compare the young and the old groups

muscle fatigue

Other

We compare the results before and after muscle fatigue

Primary outcomes

  1. Maximal force

    Time frame: Baseline (pre-fatigue protocol) and immediately after the fatigue protocol

    The maximal force of upper and lower extremity muscles

  2. Walking speed

    Time frame: Baseline (pre-fatigue protocol) and immediately after the fatigue protocol

    The time taken by participants to walk a standardized distance

  3. Step Length

    Time frame: Baseline (pre-fatigue protocol) and immediately after the fatigue protocol

    The linear distance between the two ankles, typically expressed in centimeter(cm).

  4. Cadence

    Time frame: Baseline (pre-fatigue protocol) and immediately after the fatigue protocol

    The number of steps taken per minute (SPM)

  5. Single Support Time

    Time frame: Baseline (pre-fatigue protocol) and immediately after the fatigue protocol

    The duration within the gait cycle when only one foot is in contact with the ground, typically measured in seconds or as a percentage of the total gait cycle.

  6. Double Support Time

    Time frame: Baseline (pre-fatigue protocol) and immediately after the fatigue protocol

    The portion of the gait cycle where both feet are in contact with the ground, indicating the transition phase between steps, expressed as a percentage of the gait cycle or in seconds.

  7. Swing Time

    Time frame: Baseline (pre-fatigue protocol) and immediately after the fatigue protocol

    The portion of the gait cycle where the foot is not in contact with the ground, moving forward to the next step. It is usually expressed as a percentage of the total gait cycle or in seconds.

  8. COP Velocity in Balance Tasks

    Time frame: Baseline (pre-fatigue protocol) and immediately after the fatigue protocol

    The speed at which the COP moves, calculated over the duration of the balance task. Higher velocities may reflect more dynamic balance adjustments or instability. Unit:millimeter per second(mm/s)

  9. COP Area in Balance Tasks

    Time frame: Baseline (pre-fatigue protocol) and immediately after the fatigue protocol

    The area covered by the COP trajectory during the balance task, providing an estimate of the sway envelope. A larger area might indicate poorer balance control. Unit:square millimeter(mm^2)

Secondary outcomes

  1. Oxygenated hemoglobin

    Time frame: Baseline (pre-fatigue protocol), during the fatigue protocol, and immediately after the fatigue protocol.

    Oxygenated hemoglobin is the amount of hemoglobin bound to oxygen, reflecting tissue oxygen availability. It's expressed as the percentage.

  2. Total hemoglobin

    Time frame: Baseline (pre-fatigue protocol), during the fatigue protocol, and immediately after the fatigue protocol.

    Total hemoglobin is the combined amount of oxygenated and deoxygenated hemoglobin, reflecting overall blood volume in the tissue.

  3. Deoxygenated hemoglobin

    Time frame: Baseline (pre-fatigue protocol), during the fatigue protocol, and immediately after the fatigue protocol.

    Deoxygenated hemoglobin is the amount of hemoglobin not bound to oxygen, reflecting oxygen extraction by tissues. It's expressed as the percentage.

Study contacts

Contact information is provided by the study sponsor or research team.

Chu-Ling Yen

CONTACT

[email protected]

886-3-2118800 ext. 3059

Sponsors and collaborators

Lead sponsor

Chang Gung Memorial Hospital

Other

Collaborators

  • Chang Gung University

Registry information

Important dates

Study start
2022
Primary completion
2028
Study completion
2028
First posted
Feb 12, 2026
Registry last updated
Feb 12, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.