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

23 de abril de 2026 actualizado 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.

Descripción general del estudio

Descripción detallada

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 estudio

Intervencionista

Inscripción (Actual)

14

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

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

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

Sí

Descripción

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

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación cruzada
  • Enmascaramiento: Doble

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
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
Otros nombres:
  • 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
Otros nombres:
  • 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
Otros nombres:
  • VIB+MUS

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Morning peak force production (N) measured via the Biodex Isometric MVC, with and without percutaneous stimulation.
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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 resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Morning Trail Making Test time to completion in seconds (TMT; parts A and B)
Periodo de tiempo: 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
Periodo de tiempo: 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)

Otras medidas de resultado

Medida de resultado
Medida Descripción
Periodo de tiempo
Consumo habitual de cafeína
Periodo de tiempo: Línea base
El consumo habitual de cafeína se evaluó mediante el cuestionario de consumo de cafeína (CCQ), donde se evaluó la ingesta de cafeína por la mañana, por la tarde, por la noche y durante la noche. La ingesta diaria total se expresó en mg.
Línea base
Rectal and Skin Temperature
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Publicaciones y enlaces útiles

La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.

Publicaciones Generales

  • 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

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

17 de noviembre de 2025

Finalización primaria (Actual)

19 de diciembre de 2025

Finalización del estudio (Actual)

27 de febrero de 2026

Fechas de registro del estudio

Enviado por primera vez

14 de abril de 2026

Primero enviado que cumplió con los criterios de control de calidad

23 de abril de 2026

Publicado por primera vez (Actual)

30 de abril de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

30 de abril de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

23 de abril de 2026

Última verificación

1 de abril de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • 251108LJMUREC75

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Descripción del plan IPD

IPD unavailable due to privacy or ethical restrictions

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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