Impact of Dietary Nitrate Supplementation on VO2max During Ramadan Fasting in Healthy Adults

University of Guelph

Status: Not yet enrolling

Conditions: Ramadan Fasting

Treatments: Dietary Supplement: Beetroot Juice (Beet-It Stamina Shot) & Supervised Exercise Training

Study type: Interventional

Funder types: Other

Identifiers

NCT06767176

25-01-006

Details and patient eligibility

About

The goal of this clinical trial is to determine if beetroot juice supplementation changes exercise performance following one week of Ramadan fasting in young, healthy adults. The main question it aims to answer is:

Does daily beetroot juice supplementation change VO2 max in fasting individuals during the first week of Ramadan?

Participants will:

Visit the lab before the start of Ramadan and after one week of fasting If assigned to intervention group, consume daily shots of beetroot juice (70ml) during the first week of Ramadan fasting Perform maximal exercise testing on a cycle ergometer

Full description

Recent literature demonstrates data showing a decrease in VO2max during the first week of Ramadan fasting. This is a practice observed by millions around the world every year, where individuals abstain from food and water from sunrise to sunset, dictated by the lunar calendar. Dietary nitrate consumption has been shown to increase VO2max and exercise performance. Therefore, the primary purpose of this study is to investigate whether dietary nitrate, in the form of beetroot juice, can help mitigate the decrease in VO2 max during the first week of Ramadan fasting.

24 young healthy adults will be recruited to undergo these two visits. The first visit will assess maximal oxygen uptake to determine aerobic fitness and metabolic exercise intensity zones under non-fasting conditions. The second visit will be completed after one week of Ramadan fasting. If assigned to the intervention group, participants will consume one shot (70ml) of Blonyx - Beet It Sport Nitrate 400 beetroot juice every day. Each shot contains 400mg of nitrates. Urine Specific Gravity will be measured after each visit to assess hydration status. The intervention group will also undergo Single Blood Draws after each visit to assess nitrate concentrations before and after a week of consumption.

Enrollment: 24 estimated patients

Sex: All

Ages: 18 to 50 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Free of known cardiovascular or metabolic diseases or sleep disorders
• No history of smoking (within the past 3 months)
• Able to engage in physical activity assessed through the physical activity readiness questionnaire (PAR-Q+)
• No prescription of chronic medications other than oral contraceptives
• Able to abide by fasting protocols for all visits
• Individuals who are not allergic to ultrasound gel or beetroot juice
• Individuals who are not pregnant

Exclusion criteria

• Individuals diagnosed with cardiovascular or metabolic disease or sleep disorders
• Has a history of smoking (within the past 3 months)
• Not ready to engage in physical activity as assessed by the PAR-Q+
• Individuals prescribed chronic medications other than oral contraceptives
• Unable to abide by fasting protocols for any testing visit
• Allergic to ultrasound gel or beetroot juice
• Pregnancy

Trial design

Primary purpose: Basic Science

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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24 participants in 2 patient groups

No Intervention

No Intervention group

Description:

Normal Fasting, no intervention. During this arm, participants will be asked to complete an exercise test before and after 1 week of Ramadan fasting.

Nitrate Supplementation

Experimental group

Description:

Participants will be asked to consume daily nitrate supplementation (70ml) in the form of beetroot juice for 7 days. Participants will then complete a maximal exercise test as they fast.

Treatment:

Dietary Supplement: Beetroot Juice (Beet-It Stamina Shot) & Supervised Exercise Training