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Search / Trial NCT05742373

Role of Fasted Exercise on Improving Cardiometabolic Health

Launched by MANCHESTER METROPOLITAN UNIVERSITY · Feb 23, 2023

Trial Information

Current as of August 19, 2025

Recruiting

Keywords

Cardiovascular Disease Diabetes Mellitus Obesity Cardiometabolic Health Exercise Fasted Sirtuins

ClinConnect Summary

This clinical trial is studying the effects of exercising on an empty stomach (fasted exercise) compared to exercising after eating (fed exercise) and not exercising at all (control group) on heart and metabolic health. Participants will be assigned to one of these three groups and will engage in moderate cycling exercises for four weeks, three times a week. Researchers will measure changes in health indicators, such as weight and heart health, before and after the exercise period to see how different exercise conditions affect overall health.

To be eligible for the study, participants should be between the ages of 65 and 74, non-smokers, and generally healthy, with a body mass index (BMI) over 18.5. They should not be regular exercisers, meaning they should not do more than one exercise session per week. Participants should also be free from certain health conditions and injuries that could interfere with the exercise or the study's safety. If you join the study, you can expect to complete cycling exercises while receiving support from the research team, and your health will be monitored throughout the trial.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Male or female
  • Non-smokers
  • Physically inactive (partake in no more than one exercise session per week on average)
  • Body mass index \>18.5 kg/m2
  • Healthy as assessed by medical screening questionnaire
  • Prior recipient of local anaesthetic with no known adverse effects, no known hypersensitivity or no other health issue that may constrain the administration of lidocaine hydrochloride
  • Free from musculoskeletal injury and able to perform cycling exercise
  • Capacity to give informed consent
  • Exclusion Criteria:
  • Regular exerciser
  • BMI \< 18.5 kg/m2
  • Pregnant
  • Allergy or intolerances to test meal products/ingredients (such as wheat or dairy products).
  • Recent major body weight change (+/- 3 kg in the past month)
  • Known hypersensitivity to Lidocaine Hydrochloride
  • Cardiovascular disease - complete heart block or hypovolaemia
  • Adam's-Stokes Syndrome
  • Wolff-Parkinson-White Syndrome
  • Porphyria
  • Epilepsy
  • Myasthenia Gravis
  • Other chronic medical condition or diagnosis including respiratory (eg asthma), endocrine, cardiovascular, neuromuscular disorders.
  • Taking medications or receiving treatment that may constrain the administration of lidocaine or local anaesthesia.

About Manchester Metropolitan University

Manchester Metropolitan University is a leading institution in the UK, renowned for its commitment to advancing research and innovation across various disciplines, including health and clinical sciences. The university actively engages in clinical trials aimed at improving patient outcomes and enhancing healthcare practices. With a focus on collaboration and interdisciplinary approaches, Manchester Metropolitan University leverages its diverse expertise and state-of-the-art facilities to conduct rigorous research that addresses pressing health challenges. Its dedication to ethical standards and community involvement ensures that clinical studies not only contribute to scientific knowledge but also prioritize participant welfare and societal benefit.

Locations

Manchester, Greater Manchester, United Kingdom

Patients applied

0 patients applied

Trial Officials

Adora Yau, PhD

Principal Investigator

Manchester Metropolitan University

Gethin Evans, PhD

Study Director

Manchester Metropolitan University

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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