NCT06767176

Brief Summary

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

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
21

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jan 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

January 6, 2025

Completed
Same day until next milestone

Study Start

First participant enrolled

January 6, 2025

Completed
3 days until next milestone

First Posted

Study publicly available on registry

January 9, 2025

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 31, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 31, 2025

Completed
Last Updated

May 1, 2026

Status Verified

April 1, 2026

Enrollment Period

3 months

First QC Date

January 6, 2025

Last Update Submit

April 27, 2026

Conditions

Keywords

RamadanFastingVO2maxDietary Nitrate

Outcome Measures

Primary Outcomes (1)

  • VO2 max

    Maximal Oxygen Uptakes will be assessed to analyze aerobic capacity and fitness under fasting conditions.

    One--week differences between before and after 1 week of fasting, nitrate supplementation if in intervention group

Secondary Outcomes (1)

  • Nitrate Concentration levels

    Comparison between blood before and after nitrate supplementation: one week

Study Arms (2)

No Intervention

NO INTERVENTION

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

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.

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

Interventions

7 doses, taken daily, 70 ml shots, consumed in the morning before the start of fasting

Nitrate Supplementation

Eligibility Criteria

Age18 Years - 50 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • 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

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Guelph

Guelph, Canada

Location

Related Links

MeSH Terms

Conditions

Fasting

Condition Hierarchy (Ancestors)

Feeding BehaviorBehavior

Study Officials

  • Phillip Millar, PhD

    University of Guelph

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

January 6, 2025

First Posted

January 9, 2025

Study Start

January 6, 2025

Primary Completion

March 31, 2025

Study Completion

March 31, 2025

Last Updated

May 1, 2026

Record last verified: 2026-04

Data Sharing

IPD Sharing
Will share

IPD used in the results publication

Time Frame
Beginning after publication with no end date
Access Criteria
Phillip Millar, University of Guelph

Locations