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Music ExposureNCT07558408

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

A study testing Original Music, Music intervention and Whole-body vibration in people with Music Exposure and NoMusic - Control, run by Liverpool John Moores University at 1 site in United Kingdom.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record

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Trial summary

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… Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
What is being tested?
Original Music, Music intervention and Whole-body vibration
Could I receive a placebo?
No, everyone receives an active treatment
How many people
14 participants
Where
1 siteUnited Kingdom
Study dates
17 Nov 2025to 27 Feb 2026
Phase
Interventional

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • 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

Who cannot join

  • 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

Trial locations and contacts

1 site in 1 country.

United Kingdom1 site
  • Tom Reilly Building (LJMU)

    Liverpool, Merseyside, L3 3AF

Other trials in United Kingdom

About this study

Official title: 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.

Read the detailed description

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.

  1. 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.

Being tested
Original Music, Music intervention, Control, Whole-body vibration, Whole-body vibration and music
Keywords
Music, Morning strength, Morning cognitive performance, WBV, Whole body vibration

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Original MusicOther

    ~20 Self-selected preferred "generally" motivational music between 110 to 130 bpm

  • Music interventionOther

    Same as 'Original Music' but time stretched by 15%

  • ControlOther

    No Music

  • Whole-body vibrationDevice

    Whole body vibration, for 15 minutes at 60Hz

  • Whole-body vibration and musicDevice

    Also called VIB+MUS

    Whole-body vibration for 15 minutes at 60Hz, plus Original music intervention during performance

Study groups in NCT07558408
Study groupRoleWhat they receive
Group 1Experimentali) NoMusic, ii) MUS, iii) MUS15, iv) Vibration, v) Vibration and Music
Receives: Other: Original Music; Other: Music intervention; Other: Control; Device: Whole-body vibration; Device: Whole-body vibration and music
Group 2Experimentali) MUS15, ii) Vibration, iii) NoMusic, iv) Vibration and Music v) MUS
Receives: Other: Original Music; Other: Music intervention; Other: Control; Device: Whole-body vibration; Device: Whole-body vibration and music
Group 3Experimentali)Vibration and music, ii) MUS, iii) MUS15, iv) NoMusic, v) Vibration
Receives: Other: Original Music; Other: Music intervention; Other: Control; Device: Whole-body vibration; Device: Whole-body vibration and music

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Morning peak force production (N) measured via the Biodex Isometric MVC, with and without percutaneous stimulation.

    To assess the effect of music on morning peak force production (N) measured via the Biodex Isometric MVC, with and without percutaneous stimulation.

    Measured: From familiarisation to the final experimental session (~4 weeks)

  2. Average and peak velocity

    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)

    Measured: From familiarisation to the final experimental session (~4 weeks)

  3. Average force

    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)

    Measured: From familiarisation to the final experimental session (~4 weeks)

  4. Average and peak power

    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)

    Measured: From familiarisation to the final experimental session (~4 weeks)

  5. time to peak velocity and power

    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)

    Measured: From familiarisation to the final experimental session (~4 weeks)

Secondary outcomes (2)
  1. Morning Trail Making Test time to completion in seconds (TMT; parts A and B)

    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.

    Measured: From enrolment to last experimental session (4 weeks)

  2. Morning Stroop word-color interference test

    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.

    Measured: From familiarisation to final experimental session (~4 weeks)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted30 Apr 2026
  2. Study start17 Nov 2025
  3. Primary completion19 Dec 2025
  4. Study completion27 Feb 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Crossover
Model description
Double blinded counterbalanced design with three conditions
Masking
Double blind
Who is masked
Participant, Investigator
Enrolment
14 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07558408
Sponsor's protocol ID
251108LJMUREC75
Status last verified
Apr 2026
First submitted
14 Apr 2026
Last updated
30 Apr 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: IPD unavailable due to privacy or ethical restrictions

Publications

  • 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

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