NCT07050017

Brief 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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
16

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started May 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

May 29, 2025

Completed
19 days until next milestone

First Submitted

Initial submission to the registry

June 17, 2025

Completed
16 days until next milestone

First Posted

Study publicly available on registry

July 3, 2025

Completed
26 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 29, 2025

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

September 29, 2025

Completed
Last Updated

October 6, 2025

Status Verified

October 1, 2025

Enrollment Period

2 months

First QC Date

June 17, 2025

Last Update Submit

October 2, 2025

Conditions

Keywords

milkhigh-protein milkproteinpost-exerciseappetiteenergy intake

Outcome Measures

Primary Outcomes (1)

  • energy intake

    Energy intake will be measured through an ad libitum meal provided after the exercise.

    From enrollment to the end of treatment at 3 weeks.

Secondary Outcomes (3)

  • acylated ghrelin (pg/mL)

    From enrollment to the end of treatment at 3 weeks.

  • Insulin (pmol/L)

    From enrollment to the end of treatment at 3 weeks.

  • subjective appetite

    From enrollment to the end of treatment at 3 weeks.

Study Arms (3)

carbohydrate control drink: isoenergetic and isovolumetric with milk beverages.

ACTIVE COMPARATOR

Isoenergetic and isovolumetric with milk beverages

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.

regular milk

EXPERIMENTAL

containing 15 g protein

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.

high-protein milk

EXPERIMENTAL

containing 30 g protein

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.

Interventions

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.

carbohydrate control drink: isoenergetic and isovolumetric with milk beverages.high-protein milkregular milk

Eligibility Criteria

Age18 Years - 39 Years
Sexmale(Gender-based eligibility)
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • The study will include healthy, physically active male participants aged 18-39 years who have been engaging in recreational endurance sports (such as cycling, running, triathlon, orienteering, or team sports) for at least one year, with a minimum frequency of 3 sessions per week lasting 60-90 minutes.

You may not qualify if:

  • Current smoker
  • Chronic or excessive alcohol consumption
  • Use of supplements and/or chronic medications that may affect appetite
  • Presence of cardiac, hepatic, renal, pulmonary, neurological, hematological, gastrointestinal, diabetic, thyroid, or psychiatric disorders, and/or musculoskeletal conditions that may limit exercise participation
  • Allergy or intolerance to any of the foods or beverages to be consumed during the study
  • Unstable body weight (e.g., weight loss greater than 1 kg in the past week)
  • Currently following a weight-loss diet
  • Diagnosed eating disorders or individuals who cognitively restrict food intake (to be assessed using the Three-Factor Eating Questionnaire)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Hacettepe University

Ankara, Turkey (Türkiye)

Location

Study Officials

  • muhammed atakan, Associate Professor

    Hacettepe University

    STUDY CHAIR
  • zeynep ergün, PHD student

    Hacettepe University

    STUDY CHAIR
  • süleyman bulut, Associate Professor

    Hacettepe University

    STUDY CHAIR
  • hüsrev turnagöl, professor

    Hacettepe University

    STUDY CHAIR
  • tahir hazır, professor

    Hacettepe University

    STUDY CHAIR
  • yiğitcan karanfil, Assistant professor

    Hacettepe University

    STUDY CHAIR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, CARE PROVIDER
Masking Details
The beverages will be administered in opaque bottles in a randomized order. Both the participants and the researchers will remain blinded to the content of the beverages until the end of the study.
Purpose
OTHER
Intervention Model
CROSSOVER
Model Details: All participants will attend 5 visits. Two of them are pre-screening visits.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Research Assistant

Study Record Dates

First Submitted

June 17, 2025

First Posted

July 3, 2025

Study Start

May 29, 2025

Primary Completion

July 29, 2025

Study Completion

September 29, 2025

Last Updated

October 6, 2025

Record last verified: 2025-10

Data Sharing

IPD Sharing
Will not share

Locations