NCT07405060

Brief Summary

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.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
140

participants targeted

Target at P50-P75 for all trials

Timeline
27mo left

Started Aug 2022

Longer than P75 for all trials

Geographic Reach
1 country

2 active sites

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress63%
Aug 2022Jul 2028

Study Start

First participant enrolled

August 1, 2022

Completed
3.5 years until next milestone

First Submitted

Initial submission to the registry

January 23, 2026

Completed
20 days until next milestone

First Posted

Study publicly available on registry

February 12, 2026

Completed
2.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 31, 2028

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 31, 2028

Last Updated

February 12, 2026

Status Verified

February 1, 2026

Enrollment Period

6 years

First QC Date

January 23, 2026

Last Update Submit

February 9, 2026

Conditions

Keywords

oldfatigabilitymuscle forcebalancegait performance

Outcome Measures

Primary Outcomes (9)

  • Maximal force

    The maximal force of upper and lower extremity muscles

    Baseline (pre-fatigue protocol) and immediately after the fatigue protocol

  • Walking speed

    The time taken by participants to walk a standardized distance

    Baseline (pre-fatigue protocol) and immediately after the fatigue protocol

  • Step Length

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

    Baseline (pre-fatigue protocol) and immediately after the fatigue protocol

  • Cadence

    The number of steps taken per minute (SPM)

    Baseline (pre-fatigue protocol) and immediately after the fatigue protocol

  • Single Support Time

    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.

    Baseline (pre-fatigue protocol) and immediately after the fatigue protocol

  • Double Support Time

    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.

    Baseline (pre-fatigue protocol) and immediately after the fatigue protocol

  • Swing Time

    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.

    Baseline (pre-fatigue protocol) and immediately after the fatigue protocol

  • COP Velocity in Balance Tasks

    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)

    Baseline (pre-fatigue protocol) and immediately after the fatigue protocol

  • COP Area in Balance Tasks

    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)

    Baseline (pre-fatigue protocol) and immediately after the fatigue protocol

Secondary Outcomes (3)

  • Oxygenated hemoglobin

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

  • Total hemoglobin

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

  • Deoxygenated hemoglobin

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

Study Arms (1)

Healthy people

General healthy people aged 20-40 and 60-85 years.

Other: AgeOther: Muscle fatigue

Interventions

AgeOTHER

We compare the young and the old groups

Healthy people

We compare the results before and after muscle fatigue

Healthy people

Eligibility Criteria

Age20 Years - 85 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

This study recruits healthy elderly individuals and healthy young individuals

You may qualify if:

  • 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.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

Chang Gung Memorial Hospital

Taoyuan District, Taiwan

RECRUITING

Chang Gung University

Taoyuan District, Taiwan

RECRUITING

MeSH Terms

Interventions

AgingMuscle Fatigue

Intervention Hierarchy (Ancestors)

Growth and DevelopmentPhysiological PhenomenaMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological Phenomena

Study Officials

  • Chu-Ling Yen

    Chang Gung University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant professor

Study Record Dates

First Submitted

January 23, 2026

First Posted

February 12, 2026

Study Start

August 1, 2022

Primary Completion (Estimated)

July 31, 2028

Study Completion (Estimated)

July 31, 2028

Last Updated

February 12, 2026

Record last verified: 2026-02

Locations