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NCT05121272 Clinical Trial

Fatigue and Cognitive Demand With Aging

Fatigue Clinical Trial

Official title:
Fatigue and Cognitive Demand With Aging

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT05121272
Other study ID # 13406
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date October 11, 2021
Est. completion date December 10, 2024

Study information
Verified date November 2023
Source University of Oklahoma
Contact Hugo Pereira
Phone 4053252773
Email hugomax@ou.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will determine the influence of a cognitive task performed during fatiguing contractions.

Description:

Individuals will participate in one familiarization session followed by 3 randomized experimental sessions (crossover design).

Recruitment information / eligibility
Status Recruiting
Enrollment 60
Est. completion date December 10, 2024
Est. primary completion date August 10, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria: - Healthy individuals aged between 18-35 and 65-90 Exclusion Criteria: - Metal implants or joint replacement. neuromuscular disease

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• cognitive task
cognitive task

Locations
Country Name City State
United States University of Oklahoma Norman Oklahoma

Sponsors (1)
Lead Sponsor Collaborator
University of Oklahoma

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary force Change in force of the arm muscles will be evaluated with a custom made device during each test session Each session will take approximately 2-3 hours (total of 4 test sessions)
Primary anxiety levels changes in anxiety levels quantified with a questionnaire Each session will take approximately 2-3 hours (total of 4 test sessions
Primary arterial pressure changes in arterial pressure will be quantified with a non-invasive device (finometer) Each session will take approximately 2-3 hours (total of 4 test sessions
Primary fatigue changes in fatigue will be assessed with questionnaires Each session will take approximately 2-3 hours (total of 4 test sessions
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