Impact of Protein Content of Milk on Post-Exercise Appetite and Energy Intake

NCT07050017 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 16

Last updated 2025-10-06

No results posted yet for this study

Summary

This study aims to investigate the acute effects of consuming milk beverages with different protein content on subjective appetite and energy intake in healthy adults following endurance exercise. Participants will complete an endurance exercise protocol and then consume one of three beverages: a high-protein milk, a regular-protein milk, or an isoenergetic and isovolumetric carbohydrate control drink. Subjective appetite ratings will be assessed using visual analogue scales (VAS) at multiple time points after beverage consumption. Appetite-related hormonal responses, including insulin and acylated ghrelin, will be measured via blood samples. Energy intake will be assessed through an ad libitum test meal. This study will help determine whether different types of milk consumed post-exercise influence appetite regulation, hormonal response, and subsequent energy intake.

Conditions

  • Appetite
  • Energy Intake
  • Post-exercise
  • Negative Energy Balance

Interventions

BEHAVIORAL

The study will investigate how different amounts of protein (0 g, 15 g, and 30 g) in post-exercise beverages affect appetite and energy intake following endurance exercise.

The study will investigate how different amounts of protein (carbohydrate control drink : 0 g, reguler milk : 15 g, and high-protein milk : 30 g) in post-exercise beverages affect appetite and energy intake following endurance exercise.

Sponsors & Collaborators

  • Hacettepe University

    lead OTHER

Principal Investigators

  • muhammed atakan, Associate Professor · Hacettepe University

  • zeynep ergün, PHD student · Hacettepe University

  • süleyman bulut, Associate Professor · Hacettepe University

  • hüsrev turnagöl, professor · Hacettepe University

  • tahir hazır, professor · Hacettepe University

  • yiğitcan karanfil, Assistant professor · Hacettepe University

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
39 Years
Sex
MALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-05-29
Primary Completion
2025-07-29
Completion
2025-09-29

Countries

  • Turkey (Türkiye)

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07050017 on ClinicalTrials.gov