Healthy climate-friendly dietary guidelines
BehavioralPersonalised climate-friendly healthy dietary recommendations
NCT Number: NCT05253547
The aim of the study is to provide proof of the effectiveness, acceptability, healthfulness and nutritional adequacy of dietary guidelines to reduce greenhouse gas emissions. The study will compare the effect of dietary advice based on 1) healthy climate-friendly dietary guidelines (intervention group) or 2) standard healthy dietary guidelines (control) on greenhouse gas emissions associated with dietary intake over 12 weeks.
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Notify Me18 year–64 year
All sexes
Interventional
Not applicable
University College Cork, Cork, Ireland
A randomised, parallel controlled trial will recruit n=360 healthy adults (age 18-64) across three research centres. After successful screening and receiving informed consent, participants will be randomised into the intervention or the control group for the duration of the 12-week trial described in detail in the text and figure below. The intervention group will receive dietary advice based on climate friendly eating recommendations. The control group will receive dietary recommendations based on Healthy Ireland's Healthy Eating Guidelines and Food Pyramid (FSAI, 2019).
Prior to their first onsite visit, participants will be asked to complete a Health and Lifestyle questionnaire and dietary assessment. The dietary assessment will include
Baseline, Visit 1 (Week 0): We will collect blood and urine samples from participants and record anthropometric measurements. Participants will be asked to complete a Stage of Change questionnaire to assess their openness to a diet change. All participants will complete a Food Waste Questionnaire at baseline for later comparison at endpoint. At the end of Visit 1 participants will receive a personalised feedback report and advice from nutritionists based on their habitual diet.
Week 6: Participants will be asked to complete a second dietary assessment during week 6. 3 24-hour recalls and a food frequency questionnaire will be hosted on Foodbook24, a web-based dietary recall tool.
Week 11: Before attending endpoint onsite visit, participants will complete a final dietary assessment. The same assessment as Pre-baseline and Week 6 will be used.
Endpoint, Visit 2 (Week 12): At the end of 12 weeks, participants will be invited back for a follow-up assessment. Blood and urine samples and anthropometrics will be collected/recorded. Participants will complete the Stage of Change questionnaire and Food Waste questionnaire. A Tolerance questionnaire will be administered to see how willing participants would be to continue with their prescribed diet.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Personalised climate-friendly healthy dietary recommendations
Personalised healthy dietary recommendations
Time frame: 12 weeks
Participants will record their diet at baseline (habitual diet) and endpoint (intervention diet) using an online 24-hour recall method. Diet-related greenhouse gas emissions will be estimated using food, nutrient and food-related greenhouse gas emissions databases (measured as kilograms of carbon dioxide equivalents). The primary outcome measure is the change in diet-related greenhouse gas emissions (kgCO2-eq/day) as a result of the intervention diet.
Time frame: 12 weeks
Calcium intake will be calculated using dietary intake records (3x 24-hour recalls) at baseline and endpoint (intervention diet). The secondary outcome measure is the change in calcium intake (mg/day) as a result of the intervention diet.
Time frame: 12 weeks
Iron intake will be calculated from dietary intake records (3x 24-hour recalls) at baseline and endpoint (intervention diet). The secondary outcome measure is the change in iron intake (mg/day) as a result of the intervention diet.
Time frame: 12 weeks
Participants will provide urine samples at baseline (Week 0) and endpoint (Week 12). Urinary iodine concentrations (ug/L) will be measured. The secondary outcome measure is the change in urinary iodine as a result of the intervention diet.
Time frame: 12 weeks
Participants will provide blood samples at baseline (Week 0) and endpoint (Week 12). 25(OH)D will be measured (nmol/L) as a marker of vitamin D status. The secondary outcome measure is the change in vitamin D as a result of the intervention diet.
Time frame: 12 weeks
Participants will provide blood samples at baseline (Week 0) and endpoint (Week 12). Serum lipids, including total cholesterol, HDL cholesterol and triglycerides (mmol/L) will be measured. The secondary outcome measure is the change in lipid profile as a result of the intervention diet.
Time frame: 12 weeks
Participants will provide blood samples at baseline (Week 0) and endpoint (Week 12). Fasting blood glucose will be measured (mmol/L). The secondary outcome measure is the change in fasting glucose as a result of the intervention diet.
University College Dublin
Other
Acronym: SuHeGuide
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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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