Actively Recruiting

Phase Not Applicable
Age: 18Years - 50Years
All Genders
Healthy Volunteers
NCT06997315

Bath Myorhythms Project

Led by University of Bath · Updated on 2026-05-11

30

Participants Needed

1

Research Sites

127 weeks

Total Duration

On this page

Sponsors

U

University of Bath

Lead Sponsor

U

University of Surrey

Collaborating Sponsor

AI-Summary

What this Trial Is About

Human Physiology is coordinated by a circadian timing system that synchronises daily cycles of light-dark, wake- sleep, activity-rest and feeding-fasting. The alignment of these behavioural patterns with underlying biological rhythms is closely linked to physiological function, with misalignment linked to chronic metabolic diseases. The vast majority of evidence about rhythms in metabolism comes from studies of rodents, which is remarkable given that rodents differ fundamentally from humans in both behaviour and metabolic regulation. Moreover, almost no research in any species has examined the effects of muscle contractile activity on 24-h rhythms in metabolism. Skeletal muscle is a key site of metabolic regulation and contractile activity is a powerful stimulus to increase metabolism. The researchers have established a novel protocol for serial muscle sampling throughout 24 hours and pilot work completed in preparation for this grant revealed diurnal transcriptomic and lipidomic rhythms in human skeletal muscle. Further development of that protocol has used enteral feeding via a tube which delivers nutrient directly to the stomach to enable constant nutrient delivery (including during sleep), with preliminary data indicating that underlying rhythms in metabolism are responsive to nutrient availability patterns. The researchers will now capitalise on those findings by incorporating multiple isotope tracers within the protocol, thus finally documenting the nature of rhythmic flux in carbohydrate metabolism and protein turnover in human skeletal muscle, and how those rhythms are aligned with timing and patterns of exercise. In summary, participants will stay in the laboratory for 36 hours with 24 hours of constant feeding via nasogastric tube, and muscle and blood sampling. Participants will be allocated to either the early or late exercise group (involving 1 hour of cycling at either 0800 or 2000 h, respectively) or the control group who will rest for the 24 hours.

CONDITIONS

Official Title

Bath Myorhythms Project

Who Can Participate

Age: 18Years - 50Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Women and men, with targeted recruitment to encourage female volunteers
  • Body mass index between 18 and 35 kg/m²
  • Minimum body mass of 67 kg
  • Age between 18 and 50 years
  • Premenopausal women
  • Metabolically healthy with no diagnosed metabolic illness or family history of type II diabetes
  • Able and willing to give informed oral and written consent
  • Complete and meet pre-study questionnaire and screening criteria
  • Regular sleep cycle with 6 to 8 hours of sleep per night
  • No extreme morning or evening preference
  • Agree to keep a consistent 8-hour sleep schedule within 30 minutes for one week before the study
  • Obtain 15 minutes of sunlight within 1.5 hours of waking and nap only within a 4-hour designated window for one week prior
  • Agree to wear ActiHeart and light monitors continuously and complete daily sleep and event diaries for one week before the study
  • Agree to avoid alcohol, caffeine, strenuous exercise, and certain foods for one day before the study
  • Agree to weigh and record daily meals for two days before the study
  • Agree to refrain from prescribed and over-the-counter medications and supplements affecting study outcomes for three weeks before and during the study if safe to do so
Not Eligible

You will not qualify if you...

  • Taking regular medications or supplements that cannot be stopped and that affect sleep, alertness, circadian system, metabolic, inflammatory, or endothelial functions
  • History of circadian or sleep disorders, metabolic, cardiovascular, or chronic infectious/inflammatory diseases
  • History of psychiatric or neurological disease or drug and alcohol abuse
  • Donated over 400 ml of blood in the three months before the study
  • Recent shift work involving late hours or travel across more than two time zones within three weeks before the study
  • Irregular sleep-wake cycle
  • Unable to refrain from alcohol, caffeine, strenuous exercise, or certain foods for one day before and during the study
  • Regularly consume more than 4 cups of caffeinated beverages daily
  • Smokers
  • Known allergy to lidocaine

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

University of Bath

Bath, United Kingdom, BA2 7AY

Actively Recruiting

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Research Team

J

James A Betts, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

BASIC_SCIENCE

Number of Arms

3

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