HIIT With an Eccentric Hamstring Exercise Program in Futsal Players

May 2, 2023 updated by: University of Valencia

Effects of High-intensity Interval Training With an Eccentric Hamstring Exercise Program in Futsal Players

Physiotherapy protocols based on high-intensity interval training (HIIT) or eccentric hamstring exercises like Nordic Curl (NC) have been scarcely studied in futsal players. The hypothesis of this study is that a HIIT combined with an NC exercise program is more effective than a HIIT-only program in improving physical and functional characteristics in futsal players.

Study Overview

Detailed Description

The objective of this study was to compare the effectiveness of a HIIT combined with an NC exercise program versus a HIIT-only program in futsal players. Therefore, a randomized controlled trial will be carried out. Futsal players will be divided into 1) HIIT+NC group and 2) HIIT group. The HIIT+NC group will perform a HIIT circuit combined with 3 sets of 10 NC repetitions for 4 weeks, while the HIIT group will perform the same protocol without NC exercise. BMI, intermittent work performance, vertical jump performance without and with arms, isometric strength of quadriceps and hamstrings, and the isometric H/Q ratio, will be assessed before and after the interventions.

Study Type

Interventional

Enrollment (Actual)

21

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

      • Valencia, Spain, 46010
        • University of Valencia

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

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Futsal players, over 18 years of age.

Exclusion Criteria:

  • Those who had a medical condition that prevented them from performing any of the evaluations.
  • Those who declined to participate

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: Factorial Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: HIIT and Nordic Curl exercise group
The participants will perform a weekly 50 minutes session for four weeks.
The training program in the HIIT+NC group was divided into the following parts: i) warm-up (10 minutes); ii) HIIT (25 minutes) consisting of a circuit of eight exercises; iii) Nordic curl exercise (10 mintues); and iv) stretching.
Active Comparator: HIIT-only group
The participants will perform a weekly 40 minutes session for four weeks.
The HIIT group performed the same exercises in the warm-up, HIIT and stretching sections as the HIIT+NC group, however, they did not perform the NC eccentric exercises.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Intermittent work performance
Time Frame: Baseline
Intermittent work performance will be assessed with the 30x15 Intermittence Test (30x15IFT). The speed of the test will be recorded in km/h. The higher the speed achieved, the better work performance.
Baseline
Intermittent work performance
Time Frame: After the intervention (4 weeks)
Intermittent work performance will be assessed with the 30x15 Intermittence Test (30x15IFT). The speed of the test will be recorded in km/h. The higher the speed achieved, the better the work performance.
After the intervention (4 weeks)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Vertical jump performance without arm impulse
Time Frame: Baseline
Vertical jump performance without arm impulse will be measured with the Counter Movement Jumping Test (CMJ). The jump height was calculated using the My Jump 2 program (My Jump Lab, Madrid, Spain) in cm. The higher the height achieved, the better the vertical jump performance.
Baseline
Vertical jump performance without arm impulse
Time Frame: After the intervention (4 weeks)
Vertical jump performance without arm impulse will be measured with the Counter Movement Jumping Test (CMJ). The jump height was calculated using the My Jump 2 program (My Jump Lab, Madrid, Spain) in cm. The higher the height achieved, the better the vertical jump performance.
After the intervention (4 weeks)
Vertical jump performance with arm impulse
Time Frame: Baseline
Vertical jump performance with arm impulse will be measured with the Counter Movement Jumping Test (CMJ). The jump height was calculated using the My Jump 2 program (My Jump Lab, Madrid, Spain) in cm. The higher the height achieved, the better the vertical jump performance.
Baseline
Vertical jump performance with arm impulse
Time Frame: After the intervention (4 weeks)
Vertical jump performance with arm impulse will be measured with the Counter Movement Jumping Test (CMJ). The jump height was calculated using the My Jump 2 program (My Jump Lab, Madrid, Spain) in cm. The higher the height achieved, the better the vertical jump performance.
After the intervention (4 weeks)
Maximal quadriceps isometric strength
Time Frame: Baseline
Maximal quadriceps isometric strength will be measured using the Adapted Quadriceps Sphygmomanometer Test in mmHg. The higher the pressure (mmHg) achieved, the better the quadriceps isometric strength.
Baseline
Maximal quadriceps isometric strength
Time Frame: After the intervention (4 weeks)
Maximal quadriceps isometric strength will be measured using the Adapted Quadriceps Sphygmomanometer Test in mmHg. The higher the pressure (mmHg) achieved, the better the quadriceps isometric strength.
After the intervention (4 weeks)
Maximal hamstrings isometric strength
Time Frame: Baseline
Maximal hamstrings isometric strength will be measured using the Adapted Hamstrings Sphygmomanometer Test in mmHg. The higher the pressure (mmHg) achieved, the better the hamstrings isometric strength.
Baseline
Maximal hamstrings isometric strength
Time Frame: After the intervention (4 weeks)
Maximal hamstrings isometric strength will be measured using the Adapted Hamstrings Sphygmomanometer Test in mmHg. The higher the pressure (mmHg) achieved, the better the hamstrings isometric strength.
After the intervention (4 weeks)
Isometric hamstrings/quadriceps ratio
Time Frame: Baseline
Isometric hamstrings/quadriceps (H/Q) ratio will be calculated by dividing the values obtained previously in the maximum isometric strength test of the hamstrings by those obtained in the quadriceps test. The value closer to 1, the greater the balance between the hamstrings and quadriceps muscles.
Baseline
Isometric hamstrings/quadriceps ratio
Time Frame: After the intervention (4 weeks)
Isometric hamstrings/quadriceps (H/Q) ratio will be calculated by dividing the values obtained previously in the maximum isometric strength test of the hamstrings by those obtained in the quadriceps test. The value closer to 1, the greater the balance between the hamstrings and quadriceps muscles.
After the intervention (4 weeks)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Elena Marqués Sulé, Dr, Univeristy of Valencia

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the 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 (Actual)

January 1, 2021

Primary Completion (Actual)

April 30, 2021

Study Completion (Actual)

April 30, 2021

Study Registration Dates

First Submitted

May 2, 2023

First Submitted That Met QC Criteria

May 2, 2023

First Posted (Estimate)

May 11, 2023

Study Record Updates

Last Update Posted (Estimate)

May 11, 2023

Last Update Submitted That Met QC Criteria

May 2, 2023

Last Verified

April 1, 2023

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • IE1541414

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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