Exploring fatigue and cognitive demand in different age groups
Fatigue and Cognitive Demand With Aging
NA · University of Oklahoma · NCT05121272
This study is testing how mental tasks affect tiredness during physical activity in healthy adults aged 18-35 and 65-90.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 18 Years to 90 Years |
| Sex | All |
| Sponsor | University of Oklahoma (other) |
| Locations | 1 site (Norman, Oklahoma) |
| Trial ID | NCT05121272 on ClinicalTrials.gov |
What this trial studies
This study investigates how cognitive tasks affect fatigue levels during physical exertion in individuals of varying ages. Participants will undergo a familiarization session followed by three randomized experimental sessions using a crossover design. The focus is on understanding the interplay between cognitive demand and fatigue, particularly in healthy adults aged 18-35 and 65-90. The findings may provide insights into age-related differences in fatigue response during cognitive tasks.
Who should consider this trial
Good fit: Ideal candidates for this study are healthy individuals aged between 18-35 and 65-90.
Not a fit: Patients with metal implants, joint replacements, or neuromuscular diseases may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance understanding of fatigue management in aging populations, potentially leading to improved strategies for maintaining cognitive and physical performance.
How similar studies have performed: While studies on fatigue and cognitive demand exist, this specific crossover design approach focusing on age differences is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Healthy individuals aged between 18-35 and 65-90 Exclusion Criteria: * Metal implants or joint replacement. neuromuscular disease
Where this trial is running
Norman, Oklahoma
- University of Oklahoma — Norman, Oklahoma, United States (RECRUITING)
Study contacts
- Principal investigator: Hugo Pereira, PhD — University of Oklahoma
- Study coordinator: Hugo Pereira
- Email: hugomax@ou.edu
- Phone: 4053252773
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Fatigue, sex difference, aging