Muslce Oxygenation of the Quadricep Relative to Angle and Load

NCT ID: NCT06638788

Last Updated: 2024-10-15

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: NA
• Total Enrollment: 20 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-09-30
• Study Completion Date: 2024-11-30

Brief Summary

The purpose of the present study is to determine if the amount of oxygen in muscles during resistance exercise with different weights is related to changes in torque or knee joint angle. Participants will need to come to the lab three times over three weeks. On their first visit, we will test how strong their muscles are by testing the maximal weight that can be lifted in a single repetition of a knee extension referred to as a 1 repetition maximal (1RM) followed by exercise interventions during the second and third weeks. Each exercise session will have participants lift different amounts of weight. They will use two machines: the Biodex dynamometer, that maintains constant force during a knee extension and a standard weighted knee extension machine which has variable force outputs. Participants will perform these exercises against three levels of weight, making six tests in total. Their first exercise session will take about 70 minutes and the following sessions around 55-60 minutes. They will be provided a 5-minute break between each set of lifts to ensure they are fully rested. In total, participants will be exercising for about 25-30 minutes each visit, with the rest of the time spent resting. The weights will be different percentages of the heaviest weight participants can lift.

Detailed Description

Visit 1 (70 minutes) Informed Consent and Baseline Testing Session 1

After verbal consent for participation an in-person visit will be scheduled with the associate investigator which will take place in our research space at the Chan Gunn Pavilion.

You will be asked to bring comfortable exercise clothes to this visit.

The consent form will be reviewed with you to ensure you completely understand each aspect of your involvement in the trial. If you wish to participate, you will provide written consent by signing this document in person.

Upon registration into this trial, you will complete the CSEP-Get Active Questionnaire (CSEP-GAQ), in person, which will assess your ability to safely perform exercise, as well as a general activity questionnaire to assess your exercise habits over the past 12-months. The CSEP-GAQ you complete today will be the same as the version used during your initial phone call/email screening with the study coordinator (Jacob Sanders or Ashlesh Mathrani).

Weekly physical activity will also be recorded now.

The exercise training history form will be filled out. This form will ask on average how many lower-body resistance training sets are completed per week, and on average how many minutes of lower-body moderate to vigorous physical activity are completed per week.

You will be asked to refrain from strenuous lower-body exercise for 48 hours or alcohol 12 hours before the visit, and every following visit.

We will then familiarize you with the diet and sleep forms which you will fill out at the start of every exercise intervention visit.

You will also state your dominant leg which will be used for all testing conditions

We will then randomize you to complete either variable load standard knee extensions or constant torque Biodex knee extensions in your second and third visit

You will then also be sequenced to randomly complete 20, 40, and 60% 1RM variable load standard knee extensions or constant torque Biodex knee extensions in visit 2 and 3

Upon completion of the study related forms, and randomization, height and weight will be recorded

Following these recordings, you will perform a one-repetition maximum (1RM) assessment for the knee-extension exercise on your dominant leg. This test involves slowly working up to a weight that you can move for a maximum of one full range of motion repetition.

Following the 1RM assessment, you will perform maximal isokinetic contractions on the Biodex on your dominant leg. This test involves maximum effort knee extensions at a fixed speed. This test is conducted 3 times on your dominant leg with a 2-minute rest in between tests.

Visits 2 and 3 (55/60 minutes each) Exercise Condition Visits

Visits 2 and 3 will involve a standardized warmup, filling out the sleep and diet questionnaires, and the exercise conditions in a random order. You will be asked to bring shorts and your choice of exercise top. The conditions for these visits are listed below:

Knee-extension exercises:

Dominant leg 18 repetitions at 20% 1RM set

Dominant leg 12 repetitions at 40% 1RM set

Dominant leg 6 repetitions at 60% 1RM set

Biodex exercises

Dominant leg 18 repetitions at 20% max torque set

Dominant leg 12 repetitions at 40% max torque set

Dominant leg 6 repetitions at 60% max torque set

You will arrive at the lab and will be fitted with near-infrared oxygen sensors (NIRS) on the outside of your thighs at the bottom 2/3rds between the top of the hip and the knee measuring muscle oxygenation.

You will then undergo calibration of the NIRS sensors by laying face up on a therapy table where we will then calculate your personal tourniquet pressure (PTP) on your dominant leg, a measurement used to determine pressure for a blood pressure cuff specific to your systolic blood pressure, and lower extremity limb occlusion pressure (LOP) which will determine the amount of pressure that is required for full occlusion of the arteries which will involve the cuff inflating and deflating for 20-30 seconds.

120% LOP is being used to ensure arterial flow is completely occluded. You will remain occluded until your oxygen saturation plateaus for 10 seconds (this takes between 3-5 minutes - during this time you may experience coldness/numbness in your leg and if at any point you wish to stop you can inform the research staff and the cuffs will be immediately deflated).

NIRS procedures will be performed by Jacob Sanders or Ashlesh Mathrani with specific experience and training in the procedure. These staff are not necessarily medical professionals, and it is possible that no medical professional will be in the room at the time of the procedure. Dr. Cameron Mitchell has reviewed and continues to review the performance of these procedures.

Following this plateau in saturation, the cuffs will be rapidly deflated, and you will remain face up on the therapy table until your oxygen saturation returns to resting values for two minutes.

You will then perform a general warmup on a stationary bike which will consist of 3-5 minutes of low intensity cycling at a load between 20-50W (this load will be self-selected and recorded during visit 1 and used during visits 2 and 3).

Following the general warmup you will then perform an exercise specific warmup

Six exercise tests will be performed for the variable load knee extension and constant torque Biodex knee extension split evenly with 5 minutes of rest separating sets.

Variable Load Standard Knee Extension

You will perform the knee extension exercises mentioned prior on your dominant leg and subsequently rest for 5-minutes, during which you may sit up from the leg extension machine, walk around, or use your phone/computer.

After 5 minutes of rest, you will perform the next variable load knee extension exercise test condition but this time on the dominant leg, and subsequently rest another 5 minutes.

You will repeat this procedure for the third exercise test condition as well.

All equipment used on these visits will be cleaned with disinfectant wipes before use by the next participant.

Constant Torque Biodex Dynamometer

You will perform constant torque Biodex knee extension exercises mentioned prior on your dominant leg and subsequently rest 5 minutes, during which you may sit up from the Biodex machine, walk around, or use your phone/computer.

After 5 minutes of rest, you will perform the following constant torque Biodex knee extension exercise condition and subsequently rest another 5 minutes.

After 5 minutes of rest, you will repeat the same procedure for the third exercise test condition.

All equipment used in these visits will be cleaned with disinfectant wipes following use and prior to use by the next participant.

Conditions

Healthy

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: BASIC_SCIENCE
• Blinding Strategy: NONE

Study Groups

Constant Torque Biodex Dynamometer

Participants will perform their intervention on the constant torque Biodex Dynamometer

Group Type: EXPERIMENTAL

Knee extension

Intervention Type: OTHER

Participants will perform 20, 40, and 60% of thier 1 rep maximum (1RM) at 18, 12, and 6 reps respectively.

Variable Torque Standerd Knee Extension

Participants will perform their intervention on the variable torque standerd knee extension machine

Group Type: EXPERIMENTAL

Knee extension

Intervention Type: OTHER

Participants will perform 20, 40, and 60% of thier 1 rep maximum (1RM) at 18, 12, and 6 reps respectively.

Interventions

Knee extension

Participants will perform 20, 40, and 60% of thier 1 rep maximum (1RM) at 18, 12, and 6 reps respectively.

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

1. Able to understand and communicate in English

2. All "No" answers on the CSEP Get Active questionnaire

Exclusion Criteria

1. Current use of cigarettes or other nicotine devices

2. Any major uncontrolled cardiovascular, muscular, metabolic, and/or neurological disorders

3. Any medical condition impacting the ability to participate in maximal exercise

4. Type one or type two diabetes

5. Diagnosis of cancer or undergoing cancer treatment in the past 12 months

6. Drug therapy with any drugs that alter skeletal muscle metabolism (i.e., Metformin, Benzodiazepines, hormone replacement therapy drugs)

• Minimum Eligible Age: 19 Years
• Maximum Eligible Age: 30 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

University of British Columbia

OTHER

Sponsor Role: lead

Responsible Party

Cameron Mitchell

Assistant Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Cameron Mitchell, B.kin, MSc, PhD

Role: PRINCIPAL_INVESTIGATOR

University of British Columbia

Central Contacts

Cameron Mitchell, B.kin, MSc, PhD

Role: CONTACT

cameron.mitchell@ubc.ca

604-827-2072

Other Identifiers

H24-01632

Identifier Type: -

Identifier Source: org_study_id