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NCT Number: NCT02487576

The CLOCK Study - A Human Dietary Intervention Study on Peripheral Circadian Clocks and Energy Metabolism

This human dietary intervention study with a cross-over design aims to investigate the effect of two different diurnal patterns of meal composition on peripheral circadian clocks and energy metabolism in healthy men.

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Key information

Age range

18 year–70 year

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

German Institute of Human Nutrition

Potsdam, 14558, Germany

About this study

In this cross-over study, healthy male participants are randomly allocated to one of two study groups: In study group (A) participants consume isocaloric carbohydrate-rich meals (65% Carbohydrates; 20% Fat; 15% Protein) in the morning and fat-rich meals (35% Carbohydrate; 50% Fat; 15% Protein) in the evening for four weeks. After a washout-phase participants consume isocaloric fat-rich meals in the morning and carbohydrate-rich meals in the evening for another four weeks. Study group (B) receives the same interventions in the reversed order.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • BMI between 22 kg/m² and 34,9 kg/m²
  • Normal glucose tolerance determined in a 75g-oral glucose tolerance test
  • Impaired fasting glucose determined in a 75g-oral glucose tolerance test
  • Impaired glucose tolerance determined in a 75g-oral glucose tolerance test

Exclusion criteria

  • Shift workers or history of shift work
  • Men suffering from diseases or conditions that might influence the outcome of the study. Of special interest are diseases that influence body weight regulation (enteropathy, malabsorption, hepatopathy, renal disease, endocrine disorders, diabetes mellitus, eating disorders, heart disease etc.). Also men suffering from coagulopathy, apoplexy and myocardial infarction are excluded from the study.
  • Men suffering from psychiatric disease
  • Planned changes in physical activity during the study
  • Participation in other clinical studies within the last three months
  • Weight changes > 2 kg within 2 months prior to screening day
  • Men unable to give an informed consent
  • Men unable to engage in the dietary interventions
  • Men following a special diet

Treatment and study plan

Carbohydrate-rich (HC)

Other

65% Carbohydrate; 20% Fat; 15% Protein

Fat-rich (HF)

Other

35% Carbohydrate; 50% Fat; 15% Protein

Primary outcomes

  1. Dietary-induced changes of glucose and lipid metabolism

    Time frame: week 4

  2. Effect of different diurnal patterns of meal composition on peripheral circadian clocks in blood cells and subcutaneous adipose tissue

    Time frame: week 4

Secondary outcomes

  1. Dietary-induced changes of satiety and hunger scores

    Time frame: week 4

    Measured via visual analogue scales

  2. Effect of different diurnal patterns of meal composition on Lipopolysaccharide-induced cytokine expression

    Time frame: week 4

  3. Dietary-induced changes of the human adipose tissue lipidome

    Time frame: week 4

  4. Integrative analysis of dietary-induced changes of the human adipose tissue transcriptome

    Time frame: week 4

    Microarray Analysis of adipose tissue samples

Sponsors and collaborators

Lead sponsor

German Institute of Human Nutrition

Other

Collaborators

  • Charite University, Berlin, Germany
  • German Federal Ministry of Education and Research
  • Heidelberg University
  • Max-Planck Institute of Molecular Cell Biology and Genetics

Registry information

Official study title

Interplay of Peripheral Circadian Clocks With Energy Balance and Body Weight Regulation

Acronym: CLOCK

Important dates

Study start
2014
Primary completion
2015
Study completion
2015
First posted
Jul 1, 2015
Registry last updated
Aug 26, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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