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OpenTrials
Completed

NCT Number: NCT02506218

Optimizing Meal and Snack Timing to Promote Health

This study will be conducted using standardized techniques to collect blood samples via an acute, randomized, cross-over design. Subjects will be provided all of their meals the day prior to testing and participate in 3 testing days with a minimum of 1 week break between testing days and a maximum time commitment of 7 weeks. A trained phlebotomist will place a catheter and collect blood samples from an antecubital vein using sterile techniques.

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Key information

Age range

25 year–39 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Purdue University

West Lafayette, Indiana, 47907, United States

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

25-39 years old

  • BMI between 22-37 kg/m2
  • Weight stable (± 4.5 kg) for the previous 3 months
  • Not currently (or within the past 6 months) following a vigorous exercise regimen or weight loss program
  • No acute illness
  • Not smoking
  • Not diabetic
  • Not pregnant or planning pregnancy in the next 3 months
  • Lactose tolerant
  • Willing to limit purposeful activity for 48 hours prior to each testing day
  • Willing to consume study foods and beverages.

Exclusion criteria

  • <25 or >39 years old, BMI <22 or >37 kg/m2
  • Currently (or within the past 6 months) following a vigorous exercise regimen greater than -3 - 45 minute exercise sessions per week
  • Currently following a weight loss program where subject has lost greater than 4.5 kg
  • Acute illness
  • Smoking
  • Diabetic
  • Pregnant or planning pregnancy in the next 3 months
  • Lactose intolerant
  • Unwilling to consume study foods and beverages
  • Peri and post-menopausal women.

Treatment and study plan

10 + 20 g protein consumption

Dietary Supplement

whey isolate

30 g protein breakfast

Other

30 g mixed meal breakfast

10 g protein breakfast

Other

10 g mixed meal breakfast

Primary outcomes

  1. Plasma amino acid concentration

    Time frame: 7 weeks

    Peak plasma concentration of amino acids

Secondary outcomes

  1. Blood glucose concentration

    Time frame: 7 weeks

    Area under the curve of blood glucose

Sponsors and collaborators

Lead sponsor

Purdue University

Other

Registry information

Acronym: S43

Important dates

Study start
2015
Primary completion
2016
Study completion
2016
First posted
Jul 23, 2015
Registry last updated
Jan 12, 2018

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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