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Tests a whey protein drink on blood sugar in night shift workers

Tests whey protein against a placebo in night shift workers with type 2 diabetes.

Plain-language title generated from the registry record
Registry title: Effects of an Evening PROtein PrEload on Metabolic Health in Night ShIfT Workers (PROPENSITy)

Key facts

Where
Adelaide, AustraliaSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 35 and 65 years old?

Source: NCT04869098, who can take part

Where in Australia

  • University of AdelaideAdelaide, AustraliaTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
University of Adelaide
Trial code
NCT04869098
Record updated
24 December 2024
Original description
This study will compare the effects of a whey protein supplement or a placebo consumed before the evening meal on health outcomes in night shift workers.Read full original descriptionShow less

Effects of an Evening PROtein PrEload on Blood Glucose, Metabolic Health, and Gut Hormone Release in Night ShIfT Workers (PROPENSITy)

This study will compare the effects of a whey protein supplement or a placebo consumed before the evening meal on health outcomes in night shift workers.

Inclusion: Female; Night shift workers (with a minimum of 6 months in their current shift work schedule); 35-65 years; BMI 28.0-35.0 kg/m2; waist circumference > 80cm; Weight stable in the past 6 months.

Exclusion: Personal history and/or diagnosis of: diabetes, cancer, major psychiatric disorders, liver disease, gastro-intestinal surgery or disease (including malabsorption), eating disorders, anaemia, insomnia or cardiovascular disease, and/or any other condition deemed unstable by the study physician; Participants who are taking stable doses (i.e. > 12 months) of androgenic medications (i.e. testosterone) or SSRI's will not be excluded. Personal history/diagnosis (self-reported) of diabetes (type 1 or 2), major psychiatric disorders (schizophrenia, major depressive disorder, bipolar disorder, eating disorders), gastrointestinal disorders, haematological disorders (i.e. thalassemia, iron-deficiency anaemia) insomnia, or any other medical condition, deemed unstable by the study physician; Taking medications known to alter body composition or metabolism, including (but not limited to): any medication used to lower blood glucose or antidiabetic medications (metformin, sulfonylureas, Glucagon-like peptide-1 (GLP-1) analogues [i.e. exenatide], thiazolidinediones or DPP-IV inhibitors [i.e. 'gliptins']), medications affecting weight, appetite or gut motility (i.e. diuretics, domperidone, cisapride, orlistat, phentermine, topiramate); Those working standard day time hours only, or those who work less than three to four night shifts per fortnight on average; Pregnant, planning a pregnancy or breastfeeding; Those who have lost or gained >5% of body weight in the last 6 months; Those who consume four or more standard drinks on a single occasion at a 'daily or almost daily' occurrence; current smokers of cigarettes/marijuana/e-cigarettes/vaporisers; unable to comprehend the study protocol (i.e. due to English language or cognitive difficulties).

ClinicalTrials.gov NCT04869098