- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04249986
Backpack Weight Impacts
August 1, 2024 updated by: University of California, San Francisco
Backpack Weight Impacts on Perceived Exertion and Heart Rate Variability
Backpacking is an increasingly popular outdoor recreational activity.
The base pack weight (BPW) includes gear that is not consumed or worn on the body: shelter, sleep system, weather-proofing layers and personal gear to ensure a degree of comfort and safety.
As such, reducing BPW is one of the most important tasks a backpacker manages when preparing for a trip.
Available recommendations for ideal BPW are currently inconsistent, lack clear parameters, and rely on anecdotal evidence.
The study aims to collect field data on perceived exertion and heart rate (HR) in relation to BPW during a day-long interval of hiking.
Such findings can have implications on the cost and safety profiles extending from recreational backpacking to military and wilderness rescue operations.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
20
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
-
-
California
-
Fresno, California, United States, 93703
- UCSF Fresno
-
-
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 to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Only adult (age 18-65)
- Have gone on at least two overnight backpacking trips in the past 5 years
- Have hiked at least 8 miles in a day on one of those trips
Exclusion Criteria:
- Lower extremity injuries or surgeries in the past 6-months
- Daily Smokers
- Chronic medical problems:
- Hypertension
- High cholesterol
- Diabetes
- Heart attack
- Heart surgery, cardiac catheterization, or coronary angioplasty
- Pacemaker/implantable cardiac defibrillator/rhythm disturbance
- Heart valve disease
- Heart failure
- Heart transplantation
- Congenital heart disease
- Kidney disease
- Back pain
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: Supportive Care
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: The Borg Rating of Perceived Exertion between 17 and 19 lb BPW
Participants will be randomized to both 17 and 19 pounds for the first hike and the alternate condition for the second hike.
A random number generator will create 1 block that includes 10 participants in each block to ensure comparable numbers to subjects starting at different base backpack weight.
Participants assignments will then be included in a sealed manila envelopes.
|
Participants who satisfy the exclusion criteria and health assessment instrument are categorized in the lowest risk group for cardiac events and does not require medical screening for mild to moderate exercise per ACSM guidelines.
|
|
Active Comparator: The Borg Rating of Perceived Exertion between 19 and 17 lb BPW
Participants will be randomized to both 19 or 17 pounds for the first hike and the alternate condition for the second hike.
A random number generator will create 1 block that includes 10 participants in each block to ensure comparable numbers to subjects starting at different base backpack weight.
Participants assignments will then be included in a sealed manila envelopes.
|
Participants who satisfy the exclusion criteria and health assessment instrument are categorized in the lowest risk group for cardiac events and does not require medical screening for mild to moderate exercise per ACSM guidelines.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The Borg Rating of Perceived Exertion During the Total Hike
Time Frame: 2 weeks
|
Participants will report their perceived exertion towards the end of both hikes.
The Borg Rating of Perceived Exertion scale ranges from 6 to 20. 6 being the lowest score of no exertion and 20 being the highest of maximal exertion.
|
2 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Heart Rate
Time Frame: 2 weeks
|
Difference between participants' heart rate during both 17 and 19 pound base backpack weight.
|
2 weeks
|
|
The Borg Rating of Perceived Exertion During Incline and Decline Sections of the participant
Time Frame: 2 weeks
|
Participants will report the perceived exertion mid-hike and towards the end.
The Borg Rating of Perceived Exertion scale ranges from 6 to 20. 6 being the lowest score of no exertion and 20 being the highest of maximal exertion.
|
2 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Susanne Spano, MD, University of California, San Francisco
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)
February 21, 2020
Primary Completion (Actual)
July 1, 2024
Study Completion (Actual)
July 1, 2024
Study Registration Dates
First Submitted
January 24, 2020
First Submitted That Met QC Criteria
January 28, 2020
First Posted (Actual)
January 31, 2020
Study Record Updates
Last Update Posted (Actual)
August 5, 2024
Last Update Submitted That Met QC Criteria
August 1, 2024
Last Verified
August 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- 2019126
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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