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NCT06513377Completed

Evaluating and Monitoring Physical Fatigue While Performing Functional Activities

Source: ClinicalTrials.gov · Last updated 23 Jan 2026

Brief summary (registry, in English)

Fatigue is a critical health parameter in older adults and stroke patients and is associated with negative health outcomes. Current assessment tools predominantly focus on walking related fatigue, neglecting other activities of daily living (ADLs). This study aims to fill this gap by developing a standardized, laboratory-based fatigue protocol that includes a broader range of ADLs, providing a more comprehensive fatigue assessment that's in line with the WHO vision of healthy ageing. The aim of this study is to evaluate a lab-based fatigue protocol and to unravel the relationship between physiological or movement data and perceived fatigue. Participants will take part in three separate measurement moments, during which they will execute a performance task that induces fatigue. In addition, relevant sensors will be used to collect meaningful data.

Status (registry)
Completed
Study type
Interventional
Enrollment
40 (actual)
First submitted
25 Jun 2024
Start date
20 Mar 2025
Primary completion date
15 Oct 2025
Lead sponsor
Vrije Universiteit Brussel
Diseases
Stroke
NCT number
NCT06513377

What you commit to

  • Study type: Interventional
  • Participants enrolled: 40
  • From 20 Mar 2025 to the primary completion date, 15 Oct 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Healthy physical and medical condition
    • Exclusion:
  • Physical injury or disorder that doesn't allow good physical performance

Age

  • \> 65 years old
  • \> 18 years old

Other

  • Severe problems with speech or memory which prevents the participant to understand or follow instruction
  • Co-morbidities that could influence the task execution and collected data
    • Older adults with sarcopenia:
    • Inclusion:
  • Grip strength: \< 27 kg (man) or \< 16 kg (woman)
  • Be mobile independently
    • Exclusion:
  • Severe problems with speech or memory which prevents the participant to understand or follow instruction
  • Co-morbidities that could influence the task execution and collected data
    • Healthy individuals:
    • Inclusion:

Who the study is looking for

  • \> 18 years old
  • ≥ 3 months ago stroke diagnosis
  • FAC levels 3-5

Criteria the registry did not label

  • Stroke survivors:

Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Brubotics Rehabilitation Research Center
Coordinator of this site? Confirm its status
JetteBelgiumUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.