Alterations in Gait, Strength, and Power After Ruck Marching (SPARTAN)
Primary Purpose
Exercise, Fatigue
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Loaded Walking High
Loaded Walking Mid
Walking
Sponsored by
About this trial
This is an interventional other trial for Exercise
Eligibility Criteria
Inclusion Criteria:
- Healthy, physically active individuals
- 18-39 years old
Exclusion Criteria:
- History of musculoskeletal injury within the last six months or still under a physicians care for an injury occurring more than six month prior
- History of spinal disc injury
- History of cardiovascular, metabolic, respiratory, neural, or renal disease
- No previous history or education of completing resistance exercise
- Hypertensive or tachycardic during the screening visit (SBP > 139 mmHg, DBP > 89 mmHg, heart rate > 100 bpm)
- Taking medication or supplements with a known side effect of affecting physiologic responses to exercise (e.g., beta blockers, omega-3 fatty acids, statins, aspirin)
- Any form of tobacco or nicotine use
- A positive pregnancy test at any point in the study
- Study physician discretion based on any other medical condition or medication
- Gastrointestinal disease or previous surgery prohibiting internal body temperature pill use. Subjects who have any contraindication to internal body temperature pill ingestion will be given the option to insert the pill rectally (as a suppository) or use a rectal probe.
Sites / Locations
- University at Buffalo
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Active Comparator
Experimental
Experimental
Arm Label
Unloaded Walking
Loaded Walking High
Loaded Walking Mid
Arm Description
Walking on a treadmill without wearing a pack
Walking on a treadmill while wearing a 30% body mass load with the weight placed at the high-back
Walking on a treadmill while wearing a 30% body mass load with the weight placed at the mid-back
Outcomes
Primary Outcome Measures
Change in Oxygen Consumption
Oxygen consumption will be measured using indirect calorimetry
Increased muscular jerk
Jerk will be measured using accelerometers placed at the torso and ankle
Secondary Outcome Measures
Full Information
NCT ID
NCT05309603
First Posted
March 24, 2022
Last Updated
August 15, 2023
Sponsor
State University of New York at Buffalo
1. Study Identification
Unique Protocol Identification Number
NCT05309603
Brief Title
Alterations in Gait, Strength, and Power After Ruck Marching
Acronym
SPARTAN
Official Title
Alterations in Gait, Strength, and Power After Ruck Marching
Study Type
Interventional
2. Study Status
Record Verification Date
August 2023
Overall Recruitment Status
Completed
Study Start Date
March 21, 2022 (Actual)
Primary Completion Date
July 21, 2023 (Actual)
Study Completion Date
July 21, 2023 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
State University of New York at Buffalo
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to determine change in injury risk and performance variables in males and females after walking unloaded and carrying a load with two different distributions (high-pack placement and mid-pack placement) to identify differences in injury risk
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Exercise, Fatigue
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
26 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Unloaded Walking
Arm Type
Active Comparator
Arm Description
Walking on a treadmill without wearing a pack
Arm Title
Loaded Walking High
Arm Type
Experimental
Arm Description
Walking on a treadmill while wearing a 30% body mass load with the weight placed at the high-back
Arm Title
Loaded Walking Mid
Arm Type
Experimental
Arm Description
Walking on a treadmill while wearing a 30% body mass load with the weight placed at the mid-back
Intervention Type
Other
Intervention Name(s)
Loaded Walking High
Intervention Description
Walking three miles on a treadmill at a self-selected speed while wearing a backpack with weight carried high on the back
Intervention Type
Other
Intervention Name(s)
Loaded Walking Mid
Intervention Description
Walking three miles on a treadmill at a self-selected speed while wearing a backpack with weight carried on the mid-back
Intervention Type
Other
Intervention Name(s)
Walking
Intervention Description
Walking three miles on a treadmill at a self-selected speed
Primary Outcome Measure Information:
Title
Change in Oxygen Consumption
Description
Oxygen consumption will be measured using indirect calorimetry
Time Frame
Upon completion of 3 miles of walking, an average of 45 minutes
Title
Increased muscular jerk
Description
Jerk will be measured using accelerometers placed at the torso and ankle
Time Frame
Upon completion of 3 miles of walking, an average of 45 minutes
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
39 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Healthy, physically active individuals
18-39 years old
Exclusion Criteria:
History of musculoskeletal injury within the last six months or still under a physicians care for an injury occurring more than six month prior
History of spinal disc injury
History of cardiovascular, metabolic, respiratory, neural, or renal disease
No previous history or education of completing resistance exercise
Hypertensive or tachycardic during the screening visit (SBP > 139 mmHg, DBP > 89 mmHg, heart rate > 100 bpm)
Taking medication or supplements with a known side effect of affecting physiologic responses to exercise (e.g., beta blockers, omega-3 fatty acids, statins, aspirin)
Any form of tobacco or nicotine use
A positive pregnancy test at any point in the study
Study physician discretion based on any other medical condition or medication
Gastrointestinal disease or previous surgery prohibiting internal body temperature pill use. Subjects who have any contraindication to internal body temperature pill ingestion will be given the option to insert the pill rectally (as a suppository) or use a rectal probe.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Riana Pryor, PhD
Organizational Affiliation
University at Buffalo
Official's Role
Principal Investigator
Facility Information:
Facility Name
University at Buffalo
City
Buffalo
State/Province
New York
ZIP/Postal Code
14214
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
We do not plan to share IPD with other researchers.
Learn more about this trial
Alterations in Gait, Strength, and Power After Ruck Marching
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