Fatigue and Cognitive Demand With Aging

Sponsor

University of Oklahoma (Other)

Overall Status

Recruiting

CT.gov ID

NCT05121272

Collaborator

(none)

Enrollment

Location

Arms

Anticipated Duration (Months)

2.5

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

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

Condition or Disease	Intervention/Treatment	Phase
Fatigue	Behavioral: cognitive task	N/A

Detailed Description

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

Study Design

Study Type:

Interventional

Anticipated Enrollment :

60 participants

Allocation:

Randomized

Intervention Model:

Single Group Assignment

Masking:

Single (Participant)

Primary Purpose:

Other

Official Title:

Fatigue and Cognitive Demand With Aging

Actual Study Start Date :

Oct 11, 2021

Anticipated Primary Completion Date :

Oct 10, 2023

Anticipated Study Completion Date :

Oct 10, 2023

Arms and Interventions

Arm	Intervention/Treatment
Experimental: young men Individuals will participate in 1 familiarization and 3 test sessions	Behavioral: cognitive task cognitive task
Experimental: young women Individuals will participate in 1 familiarization and 3 test sessions	Behavioral: cognitive task cognitive task
Experimental: older men Individuals will participate in 1 familiarization and 3 test sessions	Behavioral: cognitive task cognitive task
Experimental: older women Individuals will participate in 1 familiarization and 3 test sessions	Behavioral: cognitive task cognitive task

Outcome Measures

Primary Outcome Measures

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

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years to 90 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Yes

Inclusion Criteria:

Healthy individuals aged between 18-35 and 65-90

Exclusion Criteria:

Metal implants or joint replacement. neuromuscular disease

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	University of Oklahoma	Norman	Oklahoma	United States	73071

Sponsors and Collaborators

University of Oklahoma

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

Responsible Party:

University of Oklahoma

ClinicalTrials.gov Identifier:

NCT05121272

Other Study ID Numbers:

13406

First Posted:

Nov 16, 2021

Last Update Posted:

Nov 16, 2021

Last Verified:

Nov 1, 2021

Studies a U.S. FDA-regulated Drug Product:

Studies a U.S. FDA-regulated Device Product:

Keywords provided by University of Oklahoma

sex difference

aging

Additional relevant MeSH terms:

Fatigue

Study Results

No Results Posted as of Nov 16, 2021