Physiological Variables and Rowing Performance.

May 11, 2021 updated by: Tongyu Ma, Franklin Pierce University

Can Aerobic and Anaerobic Fitness Tests be Used to Track Rowing Performance Changes in Collegiate Rowers?

The purpose of this study is to investigate the association between the changes in physiological variables based on fitness testing and the changes in rowing performance.

Study Overview

Status

Completed

Conditions

Detailed Description

The literature has shown that both aerobic capacity and anaerobic capacity are important for exercise performance in rowing. Simple fitness tests (e.g., the modified Wingate test and the graded exercise test) have been validated to examine aerobic and anaerobic capacities in rowers. However, it remains unclear whether these fitness tests can be used to track rowing performance changes. The purpose of this study is to investigate the association between the changes in fitness test outcomes and the changes in rowing performance. The investigators expect that improvements in rowing performance are closely related to improvements in fitness test outcomes.

Participants will attend two sessions of fitness testing, one in the fall 2020 and one in the spring 2021. Each session will include the modified Wingate test to examine anaerobic capacity, the graded exercise test to examine the aerobic capacity, and the 2,000-meter rowing test on rowing ergometers to assess rowing performance.

Modified Wingate test:

After 3 minutes of warm-up at 40-50% of heart rate reserve, the participants will perform 30 seconds of rowing at maximal effort on the rowing ergometer.

Graded exercise test:

Workload will start from 25 Watts and it will be increased by 25 Watts by each stage until exhaustion. Each stage includes 2 minutes of rowing and 1 minute of rest.

2,000-meter rowing test: A 2,000-meter race simulation will be performed using an indoor rowing ergometer.

Study Type

Observational

Enrollment (Actual)

12

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

    • New Hampshire
      • Rindge, New Hampshire, United States, 03461
        • Franklin Pierce 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

18 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Female

Sampling Method

Non-Probability Sample

Study Population

The study population will be current rowers of a college rowing team.

Description

Inclusion Criteria:

• Collegiate rowers

Exclusion Criteria:

  • Cardiovascular diseases
  • Pulmonary diseases
  • Metabolic diseases
  • Other contraindications to exercise

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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Rowing performance
Time Frame: six months
Time to complete the 2,000-meter indoor rowing test
six months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Maximal oxygen consumption
Time Frame: six months
The highest oxygen consumption during a graded exercise test.
six months
Maximal anaerobic power
Time Frame: six months
The maximal power output during a 30-second anaerobic test.
six months

Collaborators and Investigators

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

Investigators

  • Study Director: Tongyu Ma, Ph.D., Franklin Pierce 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)

October 21, 2020

Primary Completion (ACTUAL)

May 10, 2021

Study Completion (ACTUAL)

May 10, 2021

Study Registration Dates

First Submitted

October 11, 2020

First Submitted That Met QC Criteria

October 15, 2020

First Posted (ACTUAL)

October 22, 2020

Study Record Updates

Last Update Posted (ACTUAL)

May 12, 2021

Last Update Submitted That Met QC Criteria

May 11, 2021

Last Verified

May 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • YB09042020

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

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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