Evaluating and Monitoring Physical Fatigue While Performing Functional Activities
- Conditions
- SarcopeniaStrokeFatigue
- Interventions
- Other: Performance test
- Registration Number
- NCT06513377
- Lead Sponsor
- Vrije Universiteit Brussel
- Brief Summary
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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ENROLLING_BY_INVITATION
- Sex
- All
- Target Recruitment
- 35
- > 18 years old
- ≥ 3 months ago stroke diagnosis
- FAC levels 3-5
- 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:
- > 65 years old
- 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:
- > 18 years old
- Healthy physical and medical condition
Exclusion:
- Physical injury or disorder that doesn't allow good physical performance
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description People post-stroke Performance test The intervention includes a stress test that induces progressive feelings of fatigue. Older adults with sarcopenia Performance test The intervention includes a stress test that induces progressive feelings of fatigue. Healthy individuals Performance test The intervention includes a stress test that induces progressive feelings of fatigue.
- Primary Outcome Measures
Name Time Method Changes in the Ratings of Perceived Exertion throughout the protocol execution Collected during all measurement moments (2-12 weeks). The subjective feelings of fatigue will be evaluated through the Ratings of Perceived Exertion. This will be expressed verbally by the participant throughout the execution of the protocol.
- Secondary Outcome Measures
Name Time Method Changes in muscle activity throughout the protocol execution Collected during all measurement moments (2-12 weeks). Muscle activity data (EMG) will be collected continuously throughout the protocol execution. Data acquisition will occur in a synchronized manner.
Changes in skin temperature throughout the protocol execution Collected during all measurement moments (2-12 weeks). Skin temperature data (degrees Celsius) will be collected continuously throughout the protocol execution. Data acquisition will occur in a synchronized manner.
Changes in muscle force myography throughout the protocol execution Collected during all measurement moments (2-12 weeks). Muscle force myography data will be collected continuously throughout the protocol execution. Data acquisition will occur in a synchronized manner.
Changes in heart rate (variability) throughout the protocol execution Collected during all measurement moments (2-12 weeks). Cardiorespiratory data (Heart rate) will be collected continuously throughout the protocol execution. Data acquisition will occur in a synchronized manner.
Changes in plantar pressure throughout the protocol execution Collected during all measurement moments (2-12 weeks). Plantar pressure distribution data will be collected continuously throughout the protocol execution. Data acquisition will occur in a synchronized manner.
Changes in oxygen saturation throughout the protocol execution Collected during all measurement moments (2-12 weeks). Oxygen saturation data will be collected continuously throughout the protocol execution. Data acquisition will occur in a synchronized manner.
Changes in electrodermal activity throughout the protocol execution Collected during all measurement moments (2-12 weeks). Electrodermal activity data will be collected continuously throughout the protocol execution. Data acquisition will occur in a synchronized manner.
Changes in gaze patter throughout the protocol execution Collected during all measurement moments (2-12 weeks). Eye tracking data will be collected continuously throughout the protocol execution. Data acquisition will occur in a synchronized manner.
Changes in motion data throughout the protocol execution Collected during all measurement moments (2-12 weeks). IMU data will be collected continuously throughout the protocol execution. Data acquisition will occur in a synchronized manner.
Changes in joint angles throughout the protocol execution Collected during all measurement moments (2-12 weeks). Kinematic data (degrees) will be collected continuously throughout the protocol execution. Data acquisition will occur in a synchronized manner.
Trial Locations
- Locations (1)
Brubotics Rehabilitation Research Center
🇧🇪Jette, Brussels, Belgium