- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04488445
Strength Training and Executive Functions: A Randomized Controlled Trial (ASTOEF)
November 8, 2020 updated by: Rubén López-Bueno, Universidad de Zaragoza
Acute Effects of Strength Training Over Executive Functions in Adolescents: A Randomized Controlled Trial
A group of 50 age-schooled adolescents was randomized into one intervention and another control group of 25 subjects each.
After estimating one maximum repetition for all the participants in a previous session, the intervention group performed a resistance training based on a resistance exercise of 3 sets of 3 to 5 repetitions (90% of an estimated 1 RM) whereas the control group performed both stretching and balance exercises.
Measures of executive functions ( i.e. a cognitive function associated with academic performance) were taken for all the participants before and after the training.
Both independent and paired t-test will serve to check differences between and within groups respectively.
Study Overview
Status
Unknown
Intervention / Treatment
Detailed Description
A group of 50 age-schooled adolescents was randomized into one intervention and another control group of 25 subjects each.
After estimating one maximum repetition for all the participants in a previous session, the intervention group performed a resistance training based on a resistance exercise of 3 sets of 3 to 5 repetitions (90% of an estimated 1 RM) whereas the control group performed both stretching and balance exercises.
Measures of executive functions ( i.e. a cognitive function associated with academic performance) were taken for all the participants before and after the training.
Both independent and paired t-test will serve to check differences between and within groups respectively.
The selected resistance exercise is based on a global muscle involvement.
Study Type
Interventional
Enrollment (Anticipated)
50
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
-
-
Aragón
-
Zaragoza, Aragón, Spain, 50009
- Recruiting
- University of Zaragoza
-
Contact:
- Rubén López-Bueno, MSc
- Phone Number: 0034661416735
- Email: rlopezbu@unizar.es
-
-
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
15 years to 17 years (CHILD)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Healthy age-schooled adolescent
Exclusion Criteria:
- Not healthy, injured age-schooled adolescent
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: HEALTH_SERVICES_RESEARCH
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: SINGLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
EXPERIMENTAL: Strength Training
The intervention group performs a resistance training based on a resistance exercise of 3 sets of 3 to 5 repetitions (90% of an estimated 1 RM) and 3 minutes of resting time between sets.
|
3 sets of 3 to 5 repetitions with 4 minutes of rest between sets.
90% load of 1 maximum repetition of a resistance exercise
Other Names:
|
PLACEBO_COMPARATOR: Stretching
The control group performs 3 exercises of stretching and balance during one minute each and three sets.
One minute of resting time between sets.
|
3 sets of 3 exercises of stretching and balance of one minute each.
One minute of resting time between sets.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Time to successfully complete the executive function test
Time Frame: up to 24 weeks
|
Executive function
|
up to 24 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 (ACTUAL)
September 1, 2020
Primary Completion (ACTUAL)
November 6, 2020
Study Completion (ANTICIPATED)
January 30, 2021
Study Registration Dates
First Submitted
July 18, 2020
First Submitted That Met QC Criteria
July 22, 2020
First Posted (ACTUAL)
July 28, 2020
Study Record Updates
Last Update Posted (ACTUAL)
November 10, 2020
Last Update Submitted That Met QC Criteria
November 8, 2020
Last Verified
November 1, 2020
More Information
Terms related to this study
Other Study ID Numbers
- UZaragoza13091978
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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