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Effects of Music and Vibration on Morning Muscle Strength and Cognitive Measures in Males

23 de abril de 2026 atualizado por: Joao Pedro Saes Agulhari, Liverpool John Moores University

Effects of Preferred Music Tempi and Whole-body Vibration on Morning Muscle Strength and Cognitive Measures in Males: A Standardized Approach.

Athletes often compete in the morning when they are biologically weaker; normally in competition heats or quarterfinals to qualify for the finals scheduled in the evening. Some athletes may even choose to perform at submaximal levels in these qualifying rounds, especially when they are expected to perform multiple times in the same day (such as weightlifting at the Olympic Games). Gross muscular performance such as power output or force production is greater in the evening than the morning (~3-14% variation. Similarly, time-trial performance and repeated sprint performance (RSP) a good measure of performance in team sport) is ~3 and 5 % greater in the evening than the morning. To the best of our knowledge, no study has yet investigated combined effect of vibration technology after a warm-up or music of different frequencies during testing on cognitive and physiological performance. As a daily variation in muscle strength has been widely reported in a similar population the aims of the present study are to investigate if we can improve morning muscle performance by vibration technology after a warm-up or music of different frequencies during testing on cognitive and physiological performance.

Visão geral do estudo

Descrição detalhada

Fifteen male adults. Through interviews, it was established that the volunteers had minimal knowledge of the effects of time-of-day or time-since-sleep on human performance. Verbal explanation of the experimental procedure was provided to everyone; this included the aims of the study; the possible risks associated with participation and the experimental procedures to be utilized. Any questions were answered. Individuals then provided written, informed consent before participating in the study. The experimental procedures were approved by the Human Ethics Committee at Liverpool John Moores University (ETHICS CODE: 251108LJMUREC75). The study was conducted in accordance with the ethical standards of the journal and complied with the principles of the Declaration of Helsinki.

All participants were required to visit the biomechanics laboratory (Liverpool, UK) on eight occasions. Participants completed (i) one maximum repetition (1RM) for bench press and back squat, ii) three familiarization sessions of strength and cognitive performance tests one week prior to the experimental protocol. During familiarizations participants completed a 7-day food diary that was analyzed using Nutritics® analysis software (2026, Education Edition, version 6.20, Ireland) by a SENr registered Sports and Exercise Nutritionist. The remaining sessions consisted of iii) three experimental sessions, all at least 72-h apart as a standardized recovery period. The experimental part comprised three experimental trials a) preferred music at original tempo (MUS), b) preferred music accelerated 15% (MUS15) and c) No-Music (CON)] between 07:00 and 08:40 h. Participants retired the previous night around 22:30 h, woke up at 06:30 h and arrived at the laboratory at 07:00 h in a fasted state. Participants were instructed to avoid training or intense physical activity 48 h prior to any of the visits, otherwise, participants maintained their normal daily routines. Music was delivered during strength and power measures and whilst resting through participant's own headphones in both music conditions. Loudness was normalized for both track-set and played at ~75dB to avoid practical and auditory-health concerns. Researchers and participants were blinded to intervention and conditions, track-sets were labeled MUS1 and MUS 2 and duration were matched by adding and empty track at the end of MUS15 to match duration removing biases. The order of treatment was revealed at the end of the by a researcher responsible for anonymization and randomization (JA).

All trials were performed with only one participant at a time, but with a staggered start so one participant came in at 06:45, the next 07:00 h and the last for that morning's session at 07:15 h. This scheduling for participants was kept consistent for all sessions. All participants lived no more than 15 mins away from the University laboratories. Participants were equally allocated, based on their 1RM for bench press and back squat into three groups (A, B and C), by listing 1RMs from highest to lowest and assigning letters A, B and C in order. The incidence of the learning effect was minimized by assigning the experimental conditions in counterbalanced order. The present study was carried out between the months of November to February (UK Autumn to Winter), with morning sunlight exposure limited to <80 Lux before arriving at the laboratory. The sunrise range for the duration of the study was 07:12 to 07:03 h.

2.3. Music intervention The music intervention was designed using a structured protocol informed by findings from previous experimental studies. Existing research has examined music across multiple dimensions, including preferred versus non-preferred music, fast versus slow tempo, high versus low volume, self-selected versus researcher-selected tracks, explicit versus censored content and genre differences. Based on this literature, the present intervention was developed based on modes of music selection and levels of intensity previously associated with beneficial effects on strength-endurance, maximal strength, and affective responses.

2.3.1. Post-session - Brunel music rating inventory-2 (BMRI-2) To ensure MUS was highly motivational and to understand how time-stretching may affect MUS15, participants were required to complete the BMRI-2 (BMRI PAPER REFERENCE HERE) assessing each track-set's characteristic.

2.4. Protocol and measurements: familiarization sessions The participants completed three familiarization sessions of all the strength, cognitive and questionnaire measures, before being considered as ready to participate in the study. Familiarization sessions took place at 09:30 h over a three-week period and finished one week before the study commenced to minimize learning effects. Participants arrived 0.5 hours before the start of the test and rested in a seated position, to minimize the influence of prior muscle activity. Participants completed the familiarization in the following order: i) cognitive battery of tests, ii) isometric maximal voluntary contraction (MVC) with and without percutaneous electrical stimulation, iii) back squat and bench press.

i) Cognitive battery of tests Trail Making Test (TMT; parts A and B) Rey Auditory Verbal Learning Test Stroop word-colour interference test

ii) Isometric maximal voluntary contraction Participants performed isometric MVCs of the quadriceps muscles (3 s duration), both with and without twitch interpolation percutaneous stimulation.

Twitch interpolation The quadriceps were electrically stimulated using two moistened surface electrodes which were positioned proximally over the vastus lateralis and distally over the vastus medialis. The skin was prepared prior to placement of each electrode by shaving and light abrasion of the skin, followed by cleaning with an isopropyl alcohol swab.

Voluntary Activation = = [1 - (Size of interpolated twitch / Size of resting twitch)] x 100

During familiarization sessions, participants alternated between performing MVCs with and without twitch interpolation, so that approximately three trials of each were performed within each session. Standardized strong verbal encouragement during each familiarization session/trial and real-time visual feedback of their performance was provided to the participants via the computer display onto a large screen placed in front of them.

iii) Back squat and bench press Participants were familiarized with back squat and bench press three times prior to commencement of the testing cycle. Each participant was asked to perform the back squat with incremental loads (40, 60, 80% 1RM) for one repetition at each load and 5-min rest was allowed between each effort. Likewise for bench press, each participant performed one repetition against each incremental load (40, 60 and 80 % 1RM) and again 5-min rest was given between each working effort. This was done so that the upper loads required for the experimental trials were known to be comfortably within each of the participants' physical capabilities and as such there was minimal likelihood of them failing to perform the required efforts for data collection.

2.4. Experimental Protocol and Measurements The experimental sessions took place a week after the last familiarization with 72 h recovery between the three experimental conditions. Upon arrival at the laboratory, they were asked to insert a soft flexible rectal probe, approximately 10 cm beyond the external anal sphincter. Participants then rested for 30 min in seated position to assess resting rectal temperature (Trec). Skin temperature (Tsk) was assessed simultaneously by skin thermistors, which were placed at four locations on the left side of the body. The average of the last 5 min of the 30 min resting period was recorded for resting Trec and Tsk temperatures.

Participants completed profile of mood states questionnaire, their subjective rating of sleep (using sleep questions from the Liverpool Jet lag Questionnaire; effort and rating of perceived exertion (RPE). After the initial rest measurements, participants warmed up on a cycle ergometer for 5 min at 150 W. Post warm-up, participants removed rectal probes in private and skin thermistors were taken off. After which, MVC and bench press and back squat exercises were then undertaken.

Tipo de estudo

Intervencional

Inscrição (Real)

14

Estágio

  • Não aplicável

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Locais de estudo

    • Merseyside
      • Liverpool, Merseyside, Reino Unido, L3 3AF
        • Tom Reilly Building (LJMU)

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Sim

Descrição

Inclusion Criteria:

  • Healthy adults
  • 18-35 years old
  • Injury-free
  • ≥ 2 years of weight/strength training experience
  • Not receiving any pharmacological treatment (including non-steroidal anti-inflammatory drugs, NSAIDs) throughout the study period
  • Low habitual caffeine consumers (≤ 150mg per day)
  • No preference to training regarding time-of-day

Exclusion Criteria:

  • Depressed mood (from the Beck depression inventory)
  • Poor sleep quality (a Pittsburgh sleep quality index global score >5
  • Recent shiftwork or travel across multiple time-zones
  • 'Extreme' chronotype (assessed via the Composite Morningness Questionnaire
  • Risk factors and/or symptoms of cardiovascular disease.
  • Minimal knowledge of the effects of time-of-day or time-since-sleep on human performance

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição cruzada
  • Mascaramento: Dobro

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: Group 1
i) NoMusic, ii) MUS, iii) MUS15, iv) Vibration, v) Vibration and Music
~20 Self-selected preferred "generally" motivational music between 110 to 130 bpm
Same as 'Original Music' but time stretched by 15%
No Music
Whole body vibration, for 15 minutes at 60Hz
Whole-body vibration for 15 minutes at 60Hz, plus Original music intervention during performance
Outros nomes:
  • VIB+MUS
Experimental: Group 2
i) MUS15, ii) Vibration, iii) NoMusic, iv) Vibration and Music v) MUS
~20 Self-selected preferred "generally" motivational music between 110 to 130 bpm
Same as 'Original Music' but time stretched by 15%
No Music
Whole body vibration, for 15 minutes at 60Hz
Whole-body vibration for 15 minutes at 60Hz, plus Original music intervention during performance
Outros nomes:
  • VIB+MUS
Experimental: Group 3
i)Vibration and music, ii) MUS, iii) MUS15, iv) NoMusic, v) Vibration
~20 Self-selected preferred "generally" motivational music between 110 to 130 bpm
Same as 'Original Music' but time stretched by 15%
No Music
Whole body vibration, for 15 minutes at 60Hz
Whole-body vibration for 15 minutes at 60Hz, plus Original music intervention during performance
Outros nomes:
  • VIB+MUS

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Morning peak force production (N) measured via the Biodex Isometric MVC, with and without percutaneous stimulation.
Prazo: From familiarisation to the final experimental session (~4 weeks)
To assess the effect of music on morning peak force production (N) measured via the Biodex Isometric MVC, with and without percutaneous stimulation.
From familiarisation to the final experimental session (~4 weeks)
Average and peak velocity
Prazo: From familiarisation to the final experimental session (~4 weeks)
Average and peak velocity, measure in meter per second (ms-1), for bench press and back squat at 40, 60 and 80% 1RM (maximum repetition). Body mass was factored into the back squat exercise, as this is a whole-body movement, but not into the bench press using the MuscleLab force-velocity linear encoder (Muscle Lab, Ergotest version 4010, Norway)
From familiarisation to the final experimental session (~4 weeks)
Average force
Prazo: From familiarisation to the final experimental session (~4 weeks)
Average force, measured in Newtons (N) for bench press and back squat at 40, 60 and 80% 1RM (maximum repetition). Body mass was factored into the back squat exercise, as this is a whole-body movement, but not into the bench press using the MuscleLab force-velocity linear encoder (Muscle Lab, Ergotest version 4010, Norway)
From familiarisation to the final experimental session (~4 weeks)
Average and peak power
Prazo: From familiarisation to the final experimental session (~4 weeks)
Average and peak power, measured in Watts (W) for bench press and back squat at 40, 60 and 80% 1RM (maximum repetition). Body mass was factored into the back squat exercise, as this is a whole-body movement, but not into the bench press using the MuscleLab force-velocity linear encoder (Muscle Lab, Ergotest version 4010, Norway)
From familiarisation to the final experimental session (~4 weeks)
time to peak velocity and power
Prazo: From familiarisation to the final experimental session (~4 weeks)
time to peak velocity and power, measured in seconds (s) bench press and back squat at 40, 60 and 80% 1RM (maximum repetition). Body mass was factored into the back squat exercise, as this is a whole-body movement, but not into the bench press using the MuscleLab force-velocity linear encoder (Muscle Lab, Ergotest version 4010, Norway)
From familiarisation to the final experimental session (~4 weeks)

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Morning Trail Making Test time to completion in seconds (TMT; parts A and B)
Prazo: From enrolment to last experimental session (4 weeks)
Music effects on morning Trail Making Test time to completion in seconds (TMT; parts A and B). In part A the circles are numbered 1-25, and the participant is instructed to draw lines to connect the numbers in ascending order. In part B, the circles include both numbers (1-13) and letters (A-L) and the participant is instructed to draw lines to connect the circles in ascending pattern but with the added task of alternating between numbers and letters (i.e., 1-A-2-B-3-C etc.). In both parts the participant is instructed to connect to the circles as fast as possible, without lifting the pencil from the paper. If an error is made, this is pointed out immediately and the participant is allowed to correct it. During the test, time to completion is measured, with a higher time indicative of the greater impairment.
From enrolment to last experimental session (4 weeks)
Morning Stroop word-color interference test
Prazo: From familiarisation to final experimental session (~4 weeks)
Stroop word-colour interference test. The participants were asked to read out their responses to words or colours for 45 s as quickly as possible and to leave no errors uncorrected. This was filmed and the number of errors and total amount completed was recorded and analysed. The first sheet had text (red, blue, yellow, black and green) in black ink (naming word test, W). The second sheet had blocks of colour corresponding to the text on the first sheet (naming colour test, C). With the third sheet, the participants had to read out the word (which was coloured differently to the word, e.g., the word was yellow and the colour red, referred to as the naming colour of word test, CW) and for the fourth sheet, the participants had to read out the colon (which was wrongly named, e.g., the colour was yellow but the word was red, referred to as the naming of word not colour test, WC). In this fourth sheet, the words were printed in the reverse order to the third sheet.
From familiarisation to final experimental session (~4 weeks)

Outras medidas de resultado

Medida de resultado
Descrição da medida
Prazo
Consumo habitual de cafeína
Prazo: Linha de Base
O consumo habitual de cafeína foi avaliado através do questionário de consumo de cafeína (CCQ), onde a ingestão de cafeína foi avaliada de manhã, à tarde, à noite e durante a noite. O consumo diário total foi expresso em mg.
Linha de Base
Rectal and Skin Temperature
Prazo: From familiarisation to the final experimental session (~4 weeks)

Rectal temperature by a soft flexible rectal probe (mini-thermistor, Grant instruments, Shepreth, UK) approximately 10 cm beyond the external anal sphincter. Duration in each session no longer than 35 mins.

Skin temperature (Tsk) was assessed simultaneously by skin thermistors (Grant Instruments, Squirrel 2010 series, Shepreth, UK), which were placed at four locations on the left side of the body (chest [ch], forearm [f], thigh [th] and calf [ca]). Duration in each session no longer than 35 mins.

From familiarisation to the final experimental session (~4 weeks)
Sleep questionnaires
Prazo: From familiarisation to the final experimental session (~4 weeks)
Sleep questions from the Liverpool Jet lag Questionnaire: get to sleep, how well slept, waking time and alertness after waking. Measured on a -5 (later or worst) to +5 scale (more or earlier) where ZERO is compared to normal.
From familiarisation to the final experimental session (~4 weeks)
Self-reported food diary
Prazo: Baseline
7-day food diary that was analyzed using Nutritics® analysis software by a SENr registered Sports and Exercise Nutritionist. Data is presented in macro-nutrients and micro-nutrient diet.
Baseline
chronotype
Prazo: Baseline
Extreme chronotype (assessed via the Composite Morningness Questionnaire) to assess morning, intermediate and evening types. Where Evening type scores 22 and less, Intermediate type 22-43 and Morning type 44 and above.
Baseline
Depressed mood
Prazo: Baseline
Depressed mood severity from the Beck depression inventory (BDI).21 questions were answered (with 4 answers, 0= I do not feel and 3 = I am so..). The values summated to scores where 0-9 is minimal depression, 10-18 mild and 19-29 moderate depression. 30-63 severe depression. This takes 60
Baseline

Colaboradores e Investigadores

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Publicações e links úteis

A pessoa responsável por inserir informações sobre o estudo fornece voluntariamente essas publicações. Estes podem ser sobre qualquer coisa relacionada ao estudo.

Publicações Gerais

  • DOI: 10.1111/j.1600-0838.2006.00586.x
  • https://doi.org/10.2147/CIA.S30048
  • DOI: 10.1111/sms.12979
  • DOI: 10.1177/00315125211002406
  • https://doi.org/10.3390/ jfmk6020033
  • http://dx.doi.org/10.1037/bul0000216

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

17 de novembro de 2025

Conclusão Primária (Real)

19 de dezembro de 2025

Conclusão do estudo (Real)

27 de fevereiro de 2026

Datas de inscrição no estudo

Enviado pela primeira vez

14 de abril de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

23 de abril de 2026

Primeira postagem (Real)

30 de abril de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

30 de abril de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

23 de abril de 2026

Última verificação

1 de abril de 2026

Mais Informações

Termos relacionados a este estudo

Outros números de identificação do estudo

  • 251108LJMUREC75

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

NÃO

Descrição do plano IPD

IPD unavailable due to privacy or ethical restrictions

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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