- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05500729
Hamstring/Quadriceps Ratio in CrossFit (HQCROSS)
Evaluation of Isometric Strength and Hamstring/Quadriceps Ratio in Healthy CrossFit Subjects
Crossfit® is a high-intensity physical training plan based on a program that includes exercises such as running, weight lifting and gymnastic movements. It focuses on the development of 10 physical qualities: strength, balance, cardiovascular and respiratory endurance, coordination, power, flexibility, agility, speed, precision and muscular endurance.Unfortunately, research on its effects is still at the beginning. The time of each session is one hour, which is divided into a warm-up of 10-30 minutes, strength training or skills, endurance work and finally a recovery phase, mobility and stretching. These types of exercises are incorporated into group training sessions called Workout of The Day (WOD).
Muscular strength is the action produced by a muscle or muscle group against resistance. It is one of the fundamental physical qualities for activities of daily living.
Digital isometric dynamometry is a tool to evaluate maximum voluntary isometric contraction (MVIC).
Hamstring muscles are responsible for hip extension and knee flexion. Moreover, they are the main protectors against anterior knee subluxation due to their action in conjunction with the anterior cruciate ligament (ACL).The quadriceps is one of the largest and most powerful muscles of the human body.
The ratio between hamstrings and quadriceps muscles has a strong correlation with lower limb injuries. This ratio, known as "H:Q" has proved to be the most reliable indicator to quantify a neuromuscular decompensation that causes an injury and, in addition, it is used as a prognostic indicator.
Study Overview
Status
Conditions
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
-
-
Caba
-
Ciudad Autonoma de Buenos Aires, Caba, Argentina, 1405
- Maimonides University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Regular members of Tuluka Fitness Palermo.
- With at least 1 year of Crossfit training.
Exclusion Criteria:
- Subjects with a history of knee surgery.
- Who have any type of musculoskeletal injury to the dominant lower limb.
- Who suffer from neurological disorders.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Female CrossFitters
Crossfit practitioners born as female
|
Hamstrings maximal voluntary isometric contraction (MVIC) will be measured with an isometric dynamometer (3 reps x 5 sec work x 10 sec rest).
The best rep will be used.
Whenever the third one was the best, additional measurements will be taken until a decrease in torque will be obtained to determine the maximum.
Quadriceps maximal voluntary isometric contraction (MVIC) will be measured with an isometric dynamometer (3 reps x 5 sec work x 10 sec rest).
The best rep will be used.
Whenever the third one was the best, additional measurements will be taken until a decrease in torque will be obtained to determine the maximum.
|
Male CrossFitters
Crossfit practitioners born as male
|
Hamstrings maximal voluntary isometric contraction (MVIC) will be measured with an isometric dynamometer (3 reps x 5 sec work x 10 sec rest).
The best rep will be used.
Whenever the third one was the best, additional measurements will be taken until a decrease in torque will be obtained to determine the maximum.
Quadriceps maximal voluntary isometric contraction (MVIC) will be measured with an isometric dynamometer (3 reps x 5 sec work x 10 sec rest).
The best rep will be used.
Whenever the third one was the best, additional measurements will be taken until a decrease in torque will be obtained to determine the maximum.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Hamstrings maximal voluntary isometric contraction
Time Frame: Day 1
|
Hamstrings force generated by the patient during a maximal voluntary isometric contraction, measured by an isometric dynamometer with load cell and computer interface. The best of the 3 repetitions will be considered. Whenever the third one is the best, additional measurements will be taken until a decrease in torque is obtained in order to determine the maximum. Unit: Newtons |
Day 1
|
Quadriceps maximal voluntary isometric contraction.
Time Frame: Day 1
|
Quadriceps force generated by the patient during a maximal voluntary isometric contraction, measured by an isometric dynamometer with load cell and computer interface. The best of the 3 repetitions will be considered. Whenever the third one was the best, additional measurements will be taken until a decrease in torque is obtained in order to determine the maximum. Unit: Newtons |
Day 1
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Hamstring / Quadriceps Ratio
Time Frame: Day 1
|
The ratio between hamstrings and quadriceps muscles has a strong correlation with lower limb injuries. This ratio, known as "H:Q" has proved to be the most reliable indicator to quantify a neuromuscular decompensation that causes an injury and, in addition, it is used as a prognostic indicator. Minimum value: -1 Maximum value: 1 A value below 0.6 indicates risk of injury. |
Day 1
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (ANTICIPATED)
Primary Completion (ANTICIPATED)
Study Completion (ANTICIPATED)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 5738
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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