Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04830306
Other study ID # Pro00108027
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 6, 2022
Est. completion date September 21, 2022

Study information

Verified date November 2021
Source Duke University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To compare cardiorespiratory fitness parameters (oxygen consumption and respiratory ventilation) measured during two sub-maximal exercise tests (six minute step test, 6MST & six minute walk test, 6 MWT) with maximal exercise test (cardiopulmonary exercise test, CPET)


Description:

After enrollment, the subjects will complete each of the following CRF assessments: Sub-maximal exercise test Six Minute Step Test (6MST): A face mask with the VO2 Master expired gas analysis device will be secured in position with head strap. Subjects will rest seated for 5 minutes prior to the start of the test. The subject will be given a standardized set of instructions on how to complete the test by raising each knee to 90 degrees of hip flexion. The total number of steps completed during the timed 6-minute period will be recorded. Sub-maximal exercise test Six Minute Walk Test (6MWT): A face mask with the VO2 Master expired gas analysis device will be secured in position with head strap. Subjects will rest seated for 5 minutes prior to the start of the test. A 30-m unobstructed hallway with turning points marked with small cones will be used. The subject will be given a standardized set of instructions on how to complete the test. The total distance walked during the timed 6-minute period will be recorded. Maximal exercise cardiopulmonary exercise test (CPET): The CPET is performed using an electromagnetically-braked cycle ergometer, 12-lead continuous ECG, continuous pulse oximetry, continuous expired gas analysis (oxygen and carbon dioxide) with ventilation [termed 'metabolic cart'] and intermittent non-invasive blood pressure measurement every 2 minutes. Once the subject is seated comfortably on the bike and adjusted for optimum cycling position, the face mask is fitted. The subjects are instructed on how to perform the incremental ramp test, starting with a baseline rest phase (no leg turnover) for 2 mins followed by reference phase of 2 mins of leg turnover with no resistance (0 watts). The incremental rise in work-rate from baseline is pre-determined by using the equation derived by Wasserman and colleagues in which the same work-rate is increased throughout the test to the limit of tolerance. A work-rate is selected by study staff to aim for a test duration of between 8 and 12 minutes. The subjects are instructed to maintain a cycling cadence of 55 - 65 revolutions per minute (rpm) during the exercise phase. One the limit of tolerance (maximal watts) is reached the resistance on the bike is removed () watts) and the subjects are encouraged to continue cycling for a further 2 mins during the recovery phase. The order in which 6MST and 6MWT are performed will be randomized. Between test the subjects will be allowed to rest in a chair until the heart rate is within 5 beats per min of resting values and blood pressure in within 10 mmHg of resting values. The CPET will be conducted once both 6MWT and 6MST have been completed. If the subject expresses fatigue after either 6MWT and 6MST, then the subject may elect to re-attend on a separate day to complete the evaluation. At completion of exercise evaluations the subjects will be discharged from study participation. No further follow up will be performed. Up to 40 subjects aged 18 or older will be enrolled. Inclusion Criteria: - Age 18 and older - Able to speak English - Ambulatory [assistive devices ok] - Able to provide informed consent Exclusion Criteria: - Any exclusion criteria listed in table 8 American Thoracic Society /American College of Chest Physicians Statement on CPET - Inmate of correctional facility (i.e. prisoner) - Diagnosed history of dementia - Inability to ambulate independently - Considered inappropriate to participate by Principal Investigator


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date September 21, 2022
Est. primary completion date September 21, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age 18 and older - Able to speak English - Ambulatory [assistive devices ok] - Able to provide informed consent Exclusion Criteria: - Any exclusion criteria listed in table 8 American Thoracic Society /American College of Chest Physicians Statement on CPET - Inmate of correctional facility (i.e. prisoner) - Diagnosed history of dementia - Inability to ambulate independently - Considered inappropriate to participate by Principal Investigator

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Exercise
Completion of exercise in accordance with assigned protocol

Locations

Country Name City State
United States Duke University Health System Durham North Carolina

Sponsors (1)

Lead Sponsor Collaborator
Duke University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Total amount of oxygen consumed per minute as measured by wearable face mask Oxygen measured in mL/min Up to 15 minutes
Secondary Total amount of respiratory ventilation per minute as measured by wearable face mask Respiratory ventilation measured in liters per minute Up to 15 minutes
See also
  Status Clinical Trial Phase
Recruiting NCT05496751 - Response Variability to Exercise N/A
Terminated NCT03585335 - Firefighter Cardiorespiratory Fitness (CRF) Pilot Study
Completed NCT03236363 - Effectiveness of MOVI Interventions on Adiposity, Cognition and Motor Competence: MOVI-da10! N/A
Completed NCT03236337 - Effectiveness of MOVI Interventions on Adiposity, Cognition and Subclinical Atherosclerosis: MOVI-daFit! N/A
Recruiting NCT05461001 - Sport-specific Endurance Training on Cardiorespiratory Fitness N/A
Completed NCT02224248 - Effect of Including Fitness Testing in Preventive Health Checks on Cardiorespiratory Fitness and Motivation N/A
Completed NCT06285578 - Effects of Probiotic and HIIT in Obese Women N/A
Recruiting NCT05092126 - Development & Validation of Preoperative Objective Physiological Evaluation N/A
Completed NCT05701943 - Comparison of Home- vs. Gym-based Exercise Delivery Modes N/A
Recruiting NCT06142942 - Effect of Sprint Interval Training Frequency on Improvements in Fitness N/A
Recruiting NCT05608759 - Exercise Prehabilitation for Patients With NSCLC Before Surgery N/A
Completed NCT03823664 - Cardiorespiratory Fitness in Prediabetic,Type 2 Diabetic and Healthy Individuals
Recruiting NCT05932875 - Peanut Consumption to Augment Adaptations to Concurrent Resistance and Aerobic Exercise Training N/A
Completed NCT03159949 - Sprint Snacks: The Effects of Prolonged Rest on Reduced Exertion Interval Training. N/A
Recruiting NCT05229861 - The Influence of HIIT Versus MCT on Cardiorespiratory Fitness in PPMS N/A
Completed NCT05085899 - Physical Fitness Normative Values Among School Going Children
Completed NCT03019796 - Exercise Training Effects on Metabolic Syndrome: Interactions With Medication Early Phase 1
Completed NCT03331679 - Can 2 Weeks of High Intensity Interval Training in Healthy 65-85 Year-olds Improve Cardiorespiratory Fitness? N/A
Withdrawn NCT04304092 - Addressing Individual Variability in Response to Exercise N/A
Completed NCT03194997 - Pilates and Dance to Breast Cancer Patients Undergoing Treatment N/A