- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01120808
Prevention Trial Assessing Paper-Tape in Endurance Distances (PreTAPED)
November 21, 2018 updated by: Grant S Lipman, Stanford University
Blisters are a very common complaint in both the general population and also the athlete.
This study's aim is to determine whether applying paper tape (an inexpensive and common component of most foot care kits) to the foot of endurance runners prevents the frequency and severity of friction blisters.
Study Overview
Detailed Description
Participants will be approximately 100 ultra-endurance athletes competing in Racing the Planet's 250 mile/7 day 4 Desert ultra-endurance races.
A convenience sample will be used, with full consent signed before inclusion into the study, with participants being informed that study inclusion is entirely optional and will not affect medical care.
A foot will berandomly selected for each participant, a coin will be flipped to determine which foot is to be taped, heads - right foot, and tails, left foot.
The non-taped foot will be used as a control.
No preventive treatment will be applied to the control foot.
The runner's normal sock/shoe system will be used to reflect natural wilderness conditions.
Runners will be excluded if any blisters, broken blisters, or hot spots are present on either foot at the time of initial taping as determined by visual foot inspection by a study administrator.
The participant will also be excluded if they have a pre-existing blistering condition or known sensitivity to paper tape.
Participants will have demographic data collected prior to the race, including age, gender, country of origin, number of marathons run prior, pack weight, and sock type.
The study endpoint occurs when a hot spot or blister develops on either the treated or untreated foot.
Runners will be instructed to treat suspected blisters or hot spots as they normally would, and to inform the study administrators the same day for visual inspection and final questionnaire to determine if they develop blisters or hot spots, whether they applied or re-applied tape themselves, removed tape, and the reasons for these actions.
Participants will be allowed to have their experimental taped foot re-taped by a physician at any point in the race as deemed necessary by the runner.
Before applying tape, a visual inspection will determine that feet were clean of dirt and no hot spots or blisters / broken blisters were present.
Tape will be applied by trained study physicians.
One inch micropore paper tape from 3M will be applied to each toe in the following manner.
A piece of tape will be placed on each toe longitudinally from the base of the phalanx dorsally to the base of the phalanx on the plantar side.
The tape will be smoothed against the skin.
Any tape extending beyond the tip of the phalanx will be adhered together.
A second piece of one inch paper tape will be applied circumferentially around each toe, with the ends of the tape located on the dorsum of the toe.
In this manner, all five toes on the experimental foot will be taped.
Any "dog ears" (tape extending beyond the phalanges) will be then trimmed with a scissors.
One 2 inch piece of micropore paper tape will be applied horizontally to the posterior heel over the Achilles tendon, extending from the posterior medial malleolus to the posterior lateral malleolus.
One 2 inch piece of micropore tape will be applied perpendicular to the head of the 5th metatarsal, another perpendicular to the 1st metatarsal covering medial as well as plantar aspect.
Study Type
Interventional
Enrollment (Actual)
136
Phase
- Phase 1
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
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Davis, California, United States, 95616
- University of California Davis
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Stanford, California, United States, 94305
- Stanford University School of Medicine
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-
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 75 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- All runners who are enrolled in an RTP 4 deserts event,
- All runners who are 18-75 years old, and
- All runners who speak English. The study will be enrolling only those who speak English, so they can fully understand and have knowledgeable consent to the study enrollment protocols.
Exclusion Criteria:
- Any blisters, broken blisters, or hot spots present on either foot at the time of initial taping as determined by visual foot inspection by a enrolling study physician.
- The runner has a pre-existing blistering condition.
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: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: All Participants
Participants were registered competitors in RacingThePlanet 6 stage 7 day 155mile (250km) ultramarathon.
|
Paper tape assigned to each participant's randomly selected foot.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Count of Participants With Blisters
Time Frame: 1 week
|
1 week
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
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
April 1, 2010
Primary Completion (Actual)
December 1, 2011
Study Completion (Actual)
December 1, 2011
Study Registration Dates
First Submitted
May 7, 2010
First Submitted That Met QC Criteria
May 10, 2010
First Posted (Estimate)
May 11, 2010
Study Record Updates
Last Update Posted (Actual)
December 13, 2018
Last Update Submitted That Met QC Criteria
November 21, 2018
Last Verified
November 1, 2018
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SU-04282010-5782
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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