- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03750812
The Effect of Age, Physical Fitness and a Single Bout of Aerobic Exercise on Motor and Cognitive Functions
November 21, 2018 updated by: Hillel Yaffe Medical Center
The proposed study is intended to examine the connection between two types of inhibition - cognitive and motor and the connection between motor inhibitory functions and a single bout of physical exercise in the context of age and physical fitness.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Anticipated)
120
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Hadera, Israel
- Hille Yaffe Medical Center
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
22 years to 80 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Non-smokers
- Do not take psychiatric drugs on a regular basis
- Geriatric Depression Scale score less than 3
- Mini-Mental State Examination score higher than 27
- Healthy and able to exercise at medium intensity
Exclusion Criteria:
- All others
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Highly fit older adults - Exercise
This will receive an aerobic exercise intervention
|
Medium-intense 60% heart rate reserve (HRR) aerobic exercise on a treadmill for 30 minutes
|
|
Active Comparator: Poorly fit older adults - Exercise
This arm will receive an aerobic exercise intervention
|
Medium-intense 60% heart rate reserve (HRR) aerobic exercise on a treadmill for 30 minutes
|
|
Active Comparator: Highly fit young adults - Exercise
This arm will receive an aerobic exercise intervention
|
Medium-intense 60% heart rate reserve (HRR) aerobic exercise on a treadmill for 30 minutes
|
|
Active Comparator: Poorly fit young adults - Exercise
This arm will receive an aerobic exercise intervention
|
Medium-intense 60% heart rate reserve (HRR) aerobic exercise on a treadmill for 30 minutes
|
|
Active Comparator: Highly fit older adults - TV
This arm will sit at rest and watch television
|
Sitting and watching television for 30 minutes
|
|
Active Comparator: Poorly fit older adults - TV
This arm will sit at rest and watch television
|
Sitting and watching television for 30 minutes
|
|
Active Comparator: Highly fit young adults - TV
This arm will sit at rest and watch television
|
Sitting and watching television for 30 minutes
|
|
Active Comparator: Poorly fit young adults - TV
This arm will sit at rest and watch television
|
Sitting and watching television for 30 minutes
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Improvement in cognitive functions after exercise
Time Frame: One and a half hours
|
This improvement will be measured through use of a vocal stroop test
|
One and a half hours
|
|
Improvement in motor functions after exercise
Time Frame: One and a half hours
|
This improvement will be measured through use of a multi-limb reaction time test
|
One and a half hours
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Yael Netz, PhD, Wingate Academic Institute
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Anticipated)
December 1, 2018
Primary Completion (Anticipated)
December 1, 2020
Study Completion (Anticipated)
December 1, 2020
Study Registration Dates
First Submitted
November 21, 2018
First Submitted That Met QC Criteria
November 21, 2018
First Posted (Actual)
November 23, 2018
Study Record Updates
Last Update Posted (Actual)
November 23, 2018
Last Update Submitted That Met QC Criteria
November 21, 2018
Last Verified
November 1, 2018
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- HYMC-0065-18
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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