Skip to content

The effect of red meat consumption on human metabolic and gut health in free living adults.

Investigation of the metabolic impact and gut response to regular (18% total fat) and premium (5% total fat) quality beef mince intake as part of the normal diet in healthy adults: A Pilot Study

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12619000896178
Enrollment
24
Registered
2019-06-26
Start date
2019-07-08
Completion date
Unknown
Last updated
2019-07-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

This study will investigate the effects of regular and premium grade beef mince consumption on indicators of metabolic and gut health in healthy human participants. The specific aims of this study will determine the effects of two, 1-week intervention periods on either regular or premium grade beef mince consumed at in low (65g /day) and high (130g/day) amounts. The specific aims of the study will seek to determine the metabolic and gut response to red meat as part of the habitual diet in free living healthy adults; and how the quantity (serving size) and quality (fat content) of red meat mediates these responses. By answering these questions the study will aim to generate clinically relevant results and knowledge.

Interventions

This pilot study will use a two arm randomized controlled trial design. The twenty-four (n=24) participants will be randomly split into two groups of twelve (n=12). Treatment for group 1: regular grade (18% fat) beef mince Treatment for group 2: premium grade (5% fat) beef mince All of the following study protocols are common to both groups: For the duration of the trial, free-living participants will be required to refrain from consuming any red or processed red meat, except for the red mea

This pilot study will use a two arm randomized controlled trial design. The twenty-four (n=24) participants will be randomly split into two groups of twelve (n=12). Treatment for group 1: regular grade (18% fat) beef mince Treatment for group 2: premium grade (5% fat) beef mince All of the following study protocols are common to both groups: For the duration of the trial, free-living participants will be required to refrain from consuming any red or processed red meat, except for the red meat (raw beef mince) provided to them. Red meat includes beef, veal, lamb, mutton, pork, and kangaroo. Red meat does not include poultry (e.g. chicken, turkey) or fish. Participants will be provided with an in-depth table outlining what constitutes processed red meat foods. Participants may consume processed white meat foods. To monitor adherence to the intervention, participants will be advised to record their daily food and beverage intake in food diaries for the duration of the study. The food diaries will be collected weekly. Participants will be provided with either regular grade (18% fat) or premium grade (5% fat) raw beef mince. The raw beef will be pre-portioned and provided to participants during the study along with food safety handout, however the cooking style is up to the participant. Participants will be required to cook and consume 65g of cooked mince a day in week 2, and 130g a day of cooked mince in week 3. As this is a study of habitual diet, participants can cook the meat in any way they choose. No mince is consumed in weeks 1 and 4. Week 1: Normal diet with omission of all red and processed red meat Week 2: Normal diet with 65g/day of cooked beef mince. Week 3: Normal diet with 130g/day cooked beef mince. Week 4: Normal diet with omission of al red and processed meat

Sponsors

RMIT University
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Primary purpose
Prevention

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

Healthy weight (body mass index 18.5 - 25kg/m2) males and females adults (aged 18 to 50) who are deemed eligible to participate as indicated by not meeting one or more of the exclusion criterion.

Exclusion criteria

Participants will be excluded from participating within the project for the following reasons: Individuals with presence of chronic diseases related to the metabolism of energy and nutrients (i.e. hyperthyroidism, diagnosed diabetes), pathologic eating disorders, individuals with the presence of gastrointestinal disorders and diseases (i.e. inflammatory bowel disease, irritable bowel syndrome, coeliac disease, gastroenteritis), pregnant, menopausal/post-menopausal, taking contraindicated medication (i.e. psychotropic drugs, antibiotics, immunosuppressive drugs, or appetite suppressants), the use of any dietary/nutritional supplement that might interfere with the results of the study, weight unstable in the past 3 months, or irregular bowel patterns.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026