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Effect of Exercise on Appetite in Response to Meals

Sponsor: University of Glasgow

NCT ID: NCT06096233

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Access to the study treatment being tested
Type of study
Interventional (receives a drug or procedure)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
Bouts of Exercise (other)
How long the study runs
Study runs about 35 months (dates as stated)
About the drug or intervention
Bouts of Exercise — other: The participants will run on the treadmill for 10 minutes (short) or 30 minutes (prolonged).
Patient visit burden
Not specified by the sponsor
Type of study
Testing a treatment
Ages
18 Years to 65 Years
Who
Male
Number of participants
14
Started
2023-11-06
Last checked
2026-01

Plain English Summary

What is this study?

  • • Testing a new treatment for healthy
  • • NA - 14 participants
  • • This clinical trial's primary aim is to investigate the acute effect of two exercise bouts (short \[10 minutes\] and long \[30 minutes\]) on appetite and appetite-regulatory hormone responses to a standard meal test

Who can take part?

  • • Ages 18 Years to 65 Years
  • • Diagnosed with healthy
  • • Male only

Where?

  • • Glasgow - New Lister Building at Glasgow Royal Infirmary

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

This clinical trial's primary aim is to investigate the acute effect of two exercise bouts (short \[10 minutes\] and long \[30 minutes\]) on appetite and appetite-regulatory hormone responses to a standard meal test. The secondary aim is to investigate when the changes in appetite and appetite-regulatory hormones occur during exercise. As an exploratory aim, the researchers will test if the two exercise bouts influence ad libitum energy intake in the periods after the standard meal test. The researchers will compare three groups (control, short exercise, and prolonged exercise) to see if the exercise bouts affect appetite, appetite-regulatory hormones, and energy intake in healthy men.

More detail

Study Design Screening visit Before conducting the main experiments, the participants will attend a screening visit where consent will be obtained, and they will complete questionnaires to assess health, food preferences, and physical activity. The researchers will then measure the participants' height, weight, waist circumference, and body composition. After the researchers confirm the eligibility criteria, participants will take part in two treadmill tests to establish maximum oxygen uptake test (V̇O2 max) (Broom et al. 2017). Experimental design After the screening visit, the participants will complete three main experiments (control, short high-intensity exercise, and prolonged high-intensity exercise) in a counter-balanced design. All experiments began at \~0930, following an overnight fast of at least 10 hours. Participants will consume a prescribed meal in the evening before each main experiment. Following this meal, participants are only allowed to drink water until the start of the main experiments. At the beginning of the exercise conditions, participants will run on the treadmill for 10 minutes (short) or 30 minutes (prolonged) at a speed estimated to elicit a 75% V̇O2 peak, followed by rest in the laboratory. In the control condition, the researchers will follow the same protocols except that the participants will not perform any exercise. The participants will have a standardized meal after exercise and then an ad libitum buffet meal afterward. During each experiment, the researchers will assess appetite ratings using 100 mm visual analog scales (Flint et al. 2000). The researchers will also collect blood samples to examine ghrelin, peptide YY, glucagon-like peptide 1, and possibly other blood-borne measures.

Healthy

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What we know so far

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Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 18 Years - 65 Years
  • Who can join: Male only

What the study is looking for

  • ✓Males aged 18 years or older.
  • ✓Have stable body mass for at least six months (within ±2 kg).

Who cannot take part

  • ✗Females
  • ✗People who are younger than 18 or older than 65 years old.
  • ✗Have food allergies.
  • ✗Have significant contraindications to exercise (e.g., an injury that would inhibit running).
  • ✗Smoking.
See the full criteria
Inclusion Criteria: * Males aged 18 years or older. * Have stable body mass for at least six months (within ±2 kg). Exclusion Criteria: * Females * People who are younger than 18 or older than 65 years old. * Have food allergies. * Have significant contraindications to exercise (e.g., an injury that would inhibit running). * Smoking. * Suffering from metabolic health issues, e.g., history of diabetes, cardiovascular disease, or eating disorders.

Where Is This Study? (1 UK site)

New Lister Building at Glasgow Royal Infirmary

Glasgow G31 2ER, United Kingdom

Recruiting
Site contact (verified)
James Dorling, PhDPrincipal Investigator

How to Get in Touch

Sultan Alenezi, MSc

Sponsor contact

CONTACT

+44 778 653 0734 a.sultan-kheneisr-w.1@research.gla.ac.uk

James Dorling, PhD

Sponsor contact

CONTACT

+44 141 201 6696 James.Dorling@glasgow.ac.uk
Data sourced from ClinicalTrials.gov · Last verified: 2026-01