The Effect of Quinoa on Strength, VO2max and Athletic Performance

February 20, 2025 updated by: Shibili Nuhmani, Imam Abdulrahman Bin Faisal University

The Effect of Consuming Quinoa on Muscle Strength, VO2max and Athletic Performance Among Adolescent Handball Players

Background: Proper nutrition is essential for sports performance. Quinoa is a gluten-free grain rich in macronutrients such as protein, polysaccharides, and fatty acids and consists of many phytochemicals such as carotenoids, flavonoids, saponins, fiber, vitamins, and minerals. Phytochemicals in quinoa act as antioxidant and anti-inflammatory. This will protect against several oxidative stress related diseases.

Objective: Investigate the effect of 50 g of quinoa for four weeks on muscle strength, VO2max and athletic performance among adolescent athletes.

Study design: A Double blinded randomized control trial with pre-test and post-test design.

Methods :32 subjects will be included in this trial. Subjects will be divided randomly into control and experimental group with a 1:1 ratio; the experimental group will receive two cookies that contain 50 grams of quinoa; the control group will receive the same two cookies that but without quinoa. Strength will be assessed by using hand-held dynamometer (HHD). Maximum oxygen uptake capacity (Vo2max) will be assessed by Queen's College step test (QCT). And for evaluating performance: standing long jump test, ball throw test, and agility T-test will be used. Subjects will be asked to take the cookies 1-4 hours before bedtime daily during the study period.

Statistical Analysis: Shapiro wilk test will be performed to check the normality of the data and Levenes test will be performed to check homogeneity of variance. Cohen's d will be used to check the effect size. The level of significance is set to p ≤ 0.05.

Study Overview

Study Type

Interventional

Enrollment (Actual)

32

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Dammam, Saudi Arabia, 34521
        • Imam Abdulrahman Bin Faisal University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion criteria:

1- Healthy adolescent male athletes aged 15 to 18

Exclusion criteria:

1- Use any dietary supplementation, including protein powder, during the study period.

2. Musculoskeletal, neurological, cardiovascular, or systemic disorders which may affect the testing as reported by the participants

3. Biomechanical abnormalities which may affect the testing as reported by the participants

4. Participants psychological disorders

5. Participants on medication which may affect the measurements as reported by the participants

6. Allergic from any recipe ingredients

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: N/A
  • Interventional Model: Parallel Assignment
  • Masking: Quadruple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Experimental group
the experimental group will receive two cookies that contain 50 grams of quinoa
250 grams of ground quinoa will be mixed with 250 grams of ready-to-use cookie flour and 100 gram of butter, one egg, and 75 gram of chocolate chips will be added. After mixing, the ingredients will be divided into (10) cookies (each cookie will continue 25 grams of quinoa) and bake them in oven for 9-11 mint at 190 °C. The placebo control group will receive cookies that continue the same ingredient but without quinoa and the cookies will look like the experimental group cookies. Cookies delivery will be every 3 to 4 days for each participants.
Placebo Comparator: Control group
control group will receive the same two cookies that but without quinoa
The placebo control group will receive cookies that continue the same ingredient of experimental group but without quinoa and the cookies will look like the experimental group cookies.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
strength of the biceps and triceps by Hand held dynameter
Time Frame: base line measurement and post test after 4 weeks of intervention
base line measurement and post test after 4 weeks of intervention
Maximum oxygen uptake capacity (Vo2max) assessed by Queen's College Step Test (QCT)
Time Frame: base line measurement and post test after 4 weeks of intervention
base line measurement and post test after 4 weeks of intervention
standing long jump test
Time Frame: base line measurement and post test after 4 weeks of intervention
base line measurement and post test after 4 weeks of intervention
Ball throw test
Time Frame: base line measurement and post test after 4 weeks of intervention
base line measurement and post test after 4 weeks of intervention
Agility T-test
Time Frame: base line measurement and post test after 4 weeks of intervention
base line measurement and post test after 4 weeks of intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Shibili Nuhmani, PhD, Imam Abdulrahman Bin Faisal University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

July 25, 2024

Primary Completion (Actual)

September 25, 2024

Study Completion (Actual)

October 10, 2024

Study Registration Dates

First Submitted

May 23, 2024

First Submitted That Met QC Criteria

May 30, 2024

First Posted (Actual)

June 5, 2024

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

February 20, 2025

Last Verified

July 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • IRB-PGS-2023-03-340

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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