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Impact of Reducing Dietary Intake of Red and Processed Meat Intake on Fasting Lipemia in Healthy Participants (ELM)

23 marca 2020 zaktualizowane przez: Elizabeth Simpson, University of Nottingham
Excessive meat consumption, particularly of red and processed meat, is associated with increased risk of developing a range of chronic diseases. Meat production also significantly contributes to the production of global greenhouse gasses (GHG). Given the predicted global increase in the human population, coupled with the rise in demand for meat within emerging economies, it has been suggested that strategies to alter dietary patterns and reduce meat intake should be devised. With the provision of appropriate non- or reduced-meat alternatives, this study aims to investigate whether free living subjects can significantly reduce their meat intake, and whether such dietary changes positively impact on a range of health measures

Przegląd badań

Status

Zakończony

Warunki

Interwencja / Leczenie

Szczegółowy opis

In UK adults, meat provides approximately 40% of the average daily protein intake and makes a significant contribution to intake of thiamin, niacin, vitamin B12, iron, zinc, potassium, and phosphorus. However, excessive consumption, particularly of red and processed meat, is associated with increased risk of developing a range of chronic diseases, including cardiovascular disease (CVD), obesity, type 2 diabetes and some cancers. Meat production significantly contributes to the production of greenhouse gasses (GHG) and hence global warming. Given the predicted global increase in the human population, coupled with the rise in demand for meat within emerging economies, it has been suggested that concerted efforts should be made to alter dietary patterns and reduce meat intake. Moreover, a number of reports have suggested that replacing meat with non-meat protein-rich products has health benefits. Such products tend to be inherently lower in total and saturated fat and, higher in fibre and as such, could also be cardioprotective.

The aim of this trial will be to investigate whether, with appropriate non/reduced-meat alternatives and motivational support, free living subjects can significantly reduce their meat intake and whether such dietary changes positively impact on a range of cardiovascular risk factors.

Trial design; A non-randomised, single group study design, with an initial control period will be used.

Participants; Forty healthy men and women will be recruited from the general population of Nottinghamshire, UK. All participants will attend the David Greenfield Human Physiology Unit (Queen's Medical Centre, Nottingham, UK) for an initial medical screening visit to confirm health status. In addition, blood pressure (BP) will be measured at the left upper arm (after lying semi-supine for 5min) using automated oscillometry, and body mass index (BMI) will be calculated from measured height and weight. If participants are suitable to take part with regards to their health questionnaire and BMI measures, a venous blood sample will then be taken to assess full blood count, urea, and electrolytes. Those taking lipid-lowering medication, or who report using nutritional strategies to lower their cholesterol, will be excluded. Participants will be accepted onto the trial if they report habitual consumption of 4-5 portions of red and/or processed meat per week (with 3-4 of these being consumed as main meals), they do not have food allergies related to soya or mycoprotein, and do not demonstrate any clinically significant abnormalities on screening.

Study Protocol; After recruitment, participants will be asked to record all food intake (including snacks and drinks) in a diet diary, for 4 days (3x week or work days, and 1x weekend or rest day) prior to assessment visit 1, for baseline assessment of macronutrient and energy intake. Individuals will be asked to complete further 4-day diet diaries in the week before assessment visits 2,3 and 4 (weeks 4, 10, and 16), to assess any changes in macronutrient or energy intake and meat consumption which may have occurred as a consequence of the intervention. Household measures will be used to estimate portion size, and diaries will be analysed using a food composition database. To calculate habitual diet composition, a mean daily intake will obtained from all 4 days of each recording period, and these data will be combined to produce group means.

Assessment visits will take place in the morning after the individual has fasted from midnight the night before. Initially, measurement of body mass will be made to the nearest 0.1kg using a Seca 882 Digital Scale, and waist and hip circumference will be assessed (with the participant standing) mid-way between the lowest rib and the iliac crest, and at the greater trochanters, respectively. Participants will then be asked to rest, semi-supine, on a couch for >5min before having their resting BP measured, and estimation of body composition made using bioelectrical impedance. A 5ml fasting blood sample will be taken for determination of serum insulin, total cholesterol, high density lipoprotein cholesterol (HDL), low density lipoprotein cholesterol (LDL), triacyl glycerides (TAG) and whole blood glucose. In a subset of the cohort (n=26, 13 Male:13 Female), flow mediated dilatation (FMD) will also be measured on the laboratory visits when fasted, after resting semi-supine for 1 and 2 hours.

Intervention; After visit 1 (week 0) assessment, participants will be asked not to make any changes to their lifestyle and to continue their habitual diet until visit 2 (week 4) when a second assessment will be made ('control' period). The 12 week 'intervention' period will begin on the day after the second study visit. Participants will be given information regarding how meat intake can safely be reduced in their diet, including a recipe book containing ideas for meals using meat analogues and other protein sources. A range of frozen meat-free (soya or mycoprotein 'mince', mycoprotein sausages, meatballs and 'steak strips') and reduced meat products (pork sausages, beef meatballs, beef mince and beef burgers made with 50% meat and 50% soya or mycoprotein) are available for the participants to use to aid this reduction in red meat intake. In addition, a range of dried beans (red kidney, haricot, black turtle), pulses (chick peas, green and red lentils) and grains (quinoa) will also be offered. Weekly telephone contact with the study participants will be maintained over the intervention period to improve compliance, to identify any problems and to arrange further food deliveries.

Typ studiów

Interwencyjne

Zapisy (Rzeczywisty)

37

Faza

  • Nie dotyczy

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Lokalizacje studiów

    • Notts
      • Nottingham, Notts, Zjednoczone Królestwo, NG72UH
        • David Greenfield Human Physiology Unit

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

21 lat do 50 lat (Dorosły)

Akceptuje zdrowych ochotników

Tak

Płeć kwalifikująca się do nauki

Wszystko

Opis

Inclusion Criteria:

BMI 18 - 28 kg/m2 Healthy Females should be premenopausal Good spoken and written English Consume 4-5 portions of red and/or processed meat per week consumption of greater than 70g per day

Exclusion Criteria:

Smoking Chronic diseases Hypertension Pregnancy / Breast feeding Chronic medication use (excluding oral contraceptives) Participation in any other research study three months prior to the screening or during study duration Clinically significant findings at screening

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Główny cel: Podstawowa nauka
  • Przydział: Nielosowe
  • Model interwencyjny: Zadanie dla jednej grupy
  • Maskowanie: Brak (otwarta etykieta)

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Brak interwencji: Control
Participants to continue on their habitual diet for 4 weeks
Eksperymentalny: Meat Reduction
Participants asked to reduce their red and processed meat intake by 50% for 12 weeks
Advice, Motivational material and food products provided to participants

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Fasting Serum total cholesterol concentration
Ramy czasowe: Week 0, 4,10 and 16
Fasting Serum total cholesterol concentration
Week 0, 4,10 and 16

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
Fasting Serum LDL cholesterol concentration
Ramy czasowe: Week 0, 4,10 and 16
Fasting Serum LDL cholesterol concentration
Week 0, 4,10 and 16
Fasting Serum HDL cholesterol concentration
Ramy czasowe: Week 0, 4,10 and 16
Fasting Serum HDL cholesterol concentration
Week 0, 4,10 and 16
Fasting whole blood glucose concentration
Ramy czasowe: Week 0, 4,10 and 16
Fasting whole blood glucose concentration
Week 0, 4,10 and 16
Fasting Serum Insulin concentration
Ramy czasowe: Week 0, 4,10 and 16
Fasting Serum Insulin concentration
Week 0, 4,10 and 16
Resting, supine blood pressure
Ramy czasowe: Week 0, 4,10 and 16
Resting, supine blood pressure (systolic and diastolic)
Week 0, 4,10 and 16
Body mass index calculated from measured height and weight (BMI)
Ramy czasowe: Week 0, 4,10 and 16
Body mass index calculated from measured height and weight (BMI)
Week 0, 4,10 and 16
% body fat determined by Bio-electrical Impedance
Ramy czasowe: Week 0, 4,10 and 16
% body fat determined by Bio-electrical Impedance
Week 0, 4,10 and 16
Flow-mediated dilatation
Ramy czasowe: Week 0, 4 and 16
Flow mediated dilatation at the brachial artery, measured using ultrasound (in a subset of participants)
Week 0, 4 and 16
Quality of Life Questionnaire
Ramy czasowe: Week 0, 4,10 and 16
WHOQOL Questionnaire
Week 0, 4,10 and 16
Dietary macro-nutrient intake
Ramy czasowe: Week 0, 4,10 and 16
Macro-nutrient intake of the diet determined from diet diaries
Week 0, 4,10 and 16
Dietary energy intake
Ramy czasowe: Week 0, 4,10 and 16
Energy intake of the diet determined from diet diaries
Week 0, 4,10 and 16
Meat intake
Ramy czasowe: Week 0, 4,10 and 16
daily red and processed meat intake determined from diet diaries
Week 0, 4,10 and 16
Full blood count
Ramy czasowe: Week 0,10 and 16
blood cell count, including haemoglobin
Week 0,10 and 16

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Śledczy

  • Główny śledczy: Andrew Salter, PhD, University of Nottingham

Publikacje i pomocne linki

Osoba odpowiedzialna za wprowadzenie informacji o badaniu dobrowolnie udostępnia te publikacje. Mogą one dotyczyć wszystkiego, co jest związane z badaniem.

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Rzeczywisty)

1 lipca 2015

Zakończenie podstawowe (Rzeczywisty)

1 września 2016

Ukończenie studiów (Rzeczywisty)

1 września 2016

Daty rejestracji na studia

Pierwszy przesłany

15 września 2016

Pierwszy przesłany, który spełnia kryteria kontroli jakości

19 września 2016

Pierwszy wysłany (Oszacować)

20 września 2016

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

25 marca 2020

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

23 marca 2020

Ostatnia weryfikacja

1 marca 2020

Więcej informacji

Terminy związane z tym badaniem

Inne numery identyfikacyjne badania

  • TS/L005891/1

Plan dla danych uczestnika indywidualnego (IPD)

Planujesz udostępniać dane poszczególnych uczestników (IPD)?

NIE

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