- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01241851
Effect of Acute Exercise on Cognitive Functions
November 15, 2010 updated by: Hillel Yaffe Medical Center
To determine whether acute aerobic exercise versus resistance exercise effects cognitive function among older adults.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Anticipated)
40
Phase
- Early Phase 1
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
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-
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Netanya, Israel
- Zinman College, Wingate Institute
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-
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
40 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Exercise at least 2 times a week Able to sign informed consent Able to perform ergometric exam Above 40 years old
Exclusion Criteria:
- Smoking
- Suffering psychiatric or neurologic illness
- No medication for chronic illness that could effect cognitive function
- Problems with cognitive functioning after head trauma
- Long-term hospitalization within the past 3 months
- Inability to use computer because of vision or motor problems
- Pregnancy
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: Prevention
- Allocation: Non-Randomized
- Interventional Model: Single Group Assignment
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Control
|
|
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Active Comparator: Aerobic exercise
|
|
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Active Comparator: Resistance exercise
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Level of executive function
Time Frame: One month
|
One month
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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
January 1, 2011
Primary Completion (Anticipated)
July 1, 2011
Study Completion (Anticipated)
December 1, 2011
Study Registration Dates
First Submitted
November 15, 2010
First Submitted That Met QC Criteria
November 15, 2010
First Posted (Estimate)
November 16, 2010
Study Record Updates
Last Update Posted (Estimate)
November 16, 2010
Last Update Submitted That Met QC Criteria
November 15, 2010
Last Verified
November 1, 2010
More Information
Terms related to this study
Other Study ID Numbers
- 0093-10-HYMC
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.