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NCT06724692Completed

Acute Effects of Ultra-processed Versus Unprocessed Foods on Glucocorticoid Secretion in Healthy Individuals

Source: ClinicalTrials.gov · Last updated 3 Mar 2026

Brief summary (registry, in English)

The investigators aim to understand whether the acute cortisol response to food differs between differently processed foods. In this monocentric, randomized, cross-over, open-label study, 20 healthy volunteers will receive two differently processed meals of similar caloric content and composition. The study will primarily focus on changes in blood cortisol levels, but other metabolic parameters will also be compared.

Status (registry)
Completed
Study type
Interventional
Enrollment
20 (actual)
First submitted
27 Sept 2024
Start date
30 Oct 2024
Primary completion date
4 Jul 2025
Lead sponsor
Eleonora Seelig
Diseases
Obesity
NCT number
NCT06724692

What you commit to

  • Study type: Interventional
  • Participants enrolled: 20
  • From 30 Oct 2024 to the primary completion date, 4 Jul 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previous enrollment in a clinical trial within the past two months
  • Intake of any steroid-containing drugs, including topical steroids and inhalers, within four weeks of the study initiation

Other illness

  • Severe acute or chronic disease
  • Severe food allergy

Other

  • Lactose intolerance
  • Casual smoking (more than six cigarettes per day)
  • Frequent, heavy alcohol consumption (more than 30g/day)
  • Frequent, heavy caffeine consumption (more than 4 caffeinated drinks/day)
  • Regular physical exercise (more than 4hrs per week)
  • Shift work
  • Contradictions to undergo the investigated intervention
  • Inability or unwillingness to provide informed consent

Who the study is looking for

  • Males aged 18 to 40 years
  • BMI 18.5-29.9 kg/m2

Age in the registry: 18 years to 40 years · Sex: Male · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
University Hospital Basel
Coordinator of this site? Confirm its status
BaselSwitzerlandUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.