- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04908150
Core Training Protocol vs Traditional Abdomen Exercise Protocol
May 31, 2021 updated by: Dr. Manuel González-Sánchez
A Core Training Protocol Achieves Improvements in Function, Motor Control and Endurance Strength Compared to a Traditional Abdomen Exercise Protocol: a Randomised Controlled Trial.
The main objective of this study is to analyse the effectiveness of core stability exercises to increase motor control, function and resistance strength of the abdominal muscles, compared to a traditional abdominal and trunk exercise program in semi-professionals soccer players
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The 51 participants were semi-professional soccer player and were divided into two different groups using a computer system: the CORE-group or ABDOMINALS-group.
Four weeks of training were developed.
Outcome variables: Back extension test; Flexion endurance test; FMS; functional movement screen; lateral muscle test right; lateral muscle test left.
Kinematic variables were recorded during the test using an accelerometer.
A comparison intra-group and intergroup were developed.
Study Type
Interventional
Enrollment (Actual)
51
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
-
-
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Malaga, Spain, 29071
- Manuel Gonzalez-Sanchez
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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
18 years to 30 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Male
Description
Inclusion Criteria:
- semi-professional soccer player
Exclusion Criteria:
- Participants who have suffered a musculoskeletal pathology in the lower limbs and/or having undergone some surgical intervention in the prior year were excluded
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: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Core Group
The Core Group carried out core stability exercises.
Their training consisted of the following exercises: bridge, Klapp, front plank and lateral plank
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A total of 12 sessions were carried out, which lasted for 4 weeks, with a frequency of 3 sessions/ week.
The duration of each session was 11 minutes 30 seconds.
The working time of each exercise was 30 seconds with a 5 seconds rest between exercises, meaning that each exercise cycle lasted for 2.50 seconds.
Three exercise cycles were performed with a 90 seconds rest between each one of them
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|
Active Comparator: Abdominal Group
The Abdominal Group performed traditional exercises: trunk flexion or abdominal crunch, trunk extensions, lower abdominals with hip lifts and crunch with crossed legs
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A total of 12 sessions were carried out, which lasted for 4 weeks, with a frequency of 3 sessions/ week.
The duration of each session was 11 minutes 30 seconds.
The working time of each exercise was 30 seconds with a 5 seconds rest between exercises, meaning that each exercise cycle lasted for 2.50 seconds.
Three exercise cycles were performed with a 90 seconds rest between each one of them
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Functional Movement Screen
Time Frame: 5 minutes
|
motor control and functionality in movement
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5 minutes
|
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McGill test
Time Frame: 5 minutes
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resistance strength of the abdominal muscle
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5 minutes
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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)
May 21, 2021
Primary Completion (Actual)
May 21, 2021
Study Completion (Actual)
May 21, 2021
Study Registration Dates
First Submitted
May 21, 2021
First Submitted That Met QC Criteria
May 26, 2021
First Posted (Actual)
June 1, 2021
Study Record Updates
Last Update Posted (Actual)
June 4, 2021
Last Update Submitted That Met QC Criteria
May 31, 2021
Last Verified
May 1, 2021
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 111-2020
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
publication in a scientific journal
IPD Sharing Time Frame
one month
IPD Sharing Access Criteria
open access
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
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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