Effects of Trap and Reggaeton Music on Movement Velocity, Power and Muscular Endurance in the Lower Limbs of Physically Active Women

September 29, 2023 updated by: Jimenez-Roldan Manuel Jesus, University of Seville

The influence of music on movement velocity and power during strength training have been poorly investigated, and specifically in women there is no evidence of an increase in strength performance due to the influence of music.

Hypothesis: Listening to trap or reggaeton music will improve jumping ability, as well as movement velocity and power, muscular endurance, motivation and perception of effort in trained women during the performance of back-squats.

Study Overview

Status

Completed

Detailed Description

The investigators pretend to conduct an experimental trial with a randomised crossover design in 28 participants physically active young adults with strength training experience aged 18-30 years. The study will be conducted in the laboratory of Physical Activity and Sport Sciences of the University School of Osuna.

In this way, at the end of the study the investigatos will have contrasted scientific information on the effects of music on the following variables of speed of execution in the back squat exercise.

back.

Study Type

Interventional

Enrollment (Actual)

14

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

      • Seville, Spain, 41013
        • Education Faculty

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

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • more than 6 months performing strength training programmes
  • familiarity with back squat exercises
  • no consumption of any type of nutritional supplement or anabolic substances in the three months prior to or during the same study period; v) absence of musculoskeletal injuries that may interfere with the exercise protocol during the investigation
  • absence of musculoskeletal injuries that may interfere with the exercise protocol during the investigation
  • normal hearing ability

Exclusion Criteria:

  • in addition to the above inclusion criteria, the following shall be excluded from the study participants who do not sign the informed consent form.

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: Other
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: Triple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Music

The "music" group will carry out an initial familiarisation session of the main study variables. Subsequently, through an incremental test, MR will be evaluated through the control of execution speed.

The heaviest load at which each participant could correctly lift with full knee extension shall be considered as their 1RM.

For lighter loads (average speed> 1.0 m-s-1), there will be 3 attempts per load.There shall be two attempts with medium loads(0.50 m-s-1 ≥ average speed ≤ 1.0 m-s-1); and only one for close to maximum loads (average speed < 0.50 m-s-1).

After the first 1RM visit described above, participants will complete two additional random counterbalanced visits, each with a different condition.

The music group started the whole evaluation process with the music conditioning factor present. After completion of the measurements and the necessary rest time, the measurement was repeated in the non-music condition.

After the first 1RM visit, described above, each participant will complete 2 additional randomised, counterbalanced visits, each with one condition: Music (MUS) and No Music (No-MUS). The participants will be instructed to attend the laboratory to perform the screening test in different environmental conditions that do not impact on their health status.

During the MUS session, participants will perform a back squat test and a CJM test while listening to music. The chosen songs will be at least 120 beats per minute (BPM) 15. The tempo of the music for each of the tracks will be calculated using bpm software (Tangerine!v.1.4). The music will be played using an iPhone X (Apple Inc., Cupertino, CA, USA) connected to a portable speaker (Sony MHC-V02, Sony Co., Tokyo, Japan). The sound intensity will be adjusted and standardised for all participants to 75 dB (at ear level) using the Decibel X-dBA sound level meter. Trap and reggaeton music will be played before, during and after the test.

Experimental: Non-music
The "non-music" group developed the same protocol but started the measurements without the presence of music.

After the first 1RM visit, described above, each participant will complete 2 additional randomised, counterbalanced visits, each with one condition: Music (MUS) and No Music (No-MUS). The participants will be instructed to attend the laboratory to perform the screening test in different environmental conditions that do not impact on their health status.

During the MUS session, participants will perform a back squat test and a CJM test while listening to music. The chosen songs will be at least 120 beats per minute (BPM) 15. The tempo of the music for each of the tracks will be calculated using bpm software (Tangerine!v.1.4). The music will be played using an iPhone X (Apple Inc., Cupertino, CA, USA) connected to a portable speaker (Sony MHC-V02, Sony Co., Tokyo, Japan). The sound intensity will be adjusted and standardised for all participants to 75 dB (at ear level) using the Decibel X-dBA sound level meter. Trap and reggaeton music will be played before, during and after the test.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Jumping Ability (CMJ Test)
Time Frame: up to 4 weeks

Day 1 (First situation: Music or non-music) Before assessing the participants, a warm-up with familiarisation with the CMJ will be performed. This will be followed by a short specific warm-up of 5 jumps.

After a couple of minutes of rest, the test will be performed with 3 CMJs. The jumping technique consists of a flexion-extension of hips and knees at the highest possible speed to jump as high as possible; the knee angle at maximum flexion should be close to 90° and then return to the starting position. Participants will be encouraged to perform the maximum jump height in the concentric phase of each repetition to ensure maximum muscular strength.

So, this test shall be performed at baseline and after maximal effort.

Day 2: Second situation: The same protocol but in the other situación allocated.

up to 4 weeks
Movement Velocity and Power in Back-Squat at 50% and 75% 1RM (Mean and Peak Measurements)
Time Frame: Up to 4 weeks

Day 1 (First situation: Music or non-music)

Each participant will be given the same warm-up protocol as for assessing 1RM.

After 3 min rest: Two back squats will be performed using a Smith machine while movement speed and power will be measured.

The first test will consist of 2 repetitions at 50% of 1RM.

After 3 minutes rest: The second test will be performed. It will consist of 2 repetitions at 75% of 1RM.

Both tests shall be performed at maximum speed. Participants shall be encouraged to perform the best possible effort in the concentric phase of each repetition to ensure maximum muscular strength. The average speed in m/s will be recorded for both repetitions, as well as the maximum speed of both squats (at 50% and 75% of 1RM). The velocity of movement will be monitored by the researchers using a validated linear position transducer.

Day 2: Second situation: The same protocol but in the other situación allocated.

Up to 4 weeks
Muscular Endurance
Time Frame: Up to 4 weeks

Day 1 (First situation: Music or non-music)

After 3 minutes rest, a test shall be performed to calculate the maximum number or repetitions to concentric failure at 75% of 1RM.

Day 2: Second situation: The same protocol but in the other situación allocated.

Up to 4 weeks
Participants motivation through an Analogic Visual Scale (AVS)
Time Frame: Up to 4 weeks

Day 1 (First situation: Music or non-music)

The AVS will consist of a 100 mm straight line where 0 mm indicates "no motivation", while 100 mm indicates "extremely motivated". Participants will mark on the line how motivated they feel during the exercise. Researchers will then record the distance between 0 mm and the mark participants place on the line.

Day 2: Second situation: the same protocol but in the other situación allocated.

Up to 4 weeks
Participants Perceived Effort
Time Frame: Up to 4 weeks

Day 1 (First situation: Music or non-music)

As soon as participants complete the muscular endurance test, perceived exertion will be assessed on a scale of 0 (minimun) to 10 (maximum). The answers given will be recorded by the researchers.

Day 2: Second situation: the same protocol but in the other situación allocated.

Up to 4 weeks

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 (Actual)

June 1, 2023

Primary Completion (Actual)

June 15, 2023

Study Completion (Actual)

June 30, 2023

Study Registration Dates

First Submitted

September 5, 2023

First Submitted That Met QC Criteria

September 29, 2023

First Posted (Actual)

October 6, 2023

Study Record Updates

Last Update Posted (Actual)

October 6, 2023

Last Update Submitted That Met QC Criteria

September 29, 2023

Last Verified

September 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • Trap_Strength_women

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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