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Effect of Exercise on Appetite in Response to Meals

U

University of Glasgow

Status

Enrolling

Conditions

Healthy

Treatments

Other: Bouts of Exercise

Study type

Interventional

Funder types

Other

Identifiers

NCT06096233
200220449

Details and patient eligibility

About

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.

Full description

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.

Enrollment

14 estimated patients

Sex

Male

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

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.

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

14 participants in 3 patient groups

Control
No Intervention group
Description:
The participants will not perform any exercise.
Short Exercise
Experimental group
Description:
The participants will run on the treadmill for 10 minutes.
Treatment:
Other: Bouts of Exercise
Prolonged Exercise
Experimental group
Description:
The participants will run on the treadmill for 30 minutes.
Treatment:
Other: Bouts of Exercise

Trial contacts and locations

1

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Central trial contact

James Dorling, PhD; Sultan Alenezi, MSc

Data sourced from clinicaltrials.gov

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