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NCT04531306 · ClinicalTrials.gov registry record · NA
An Analysis of Kinesio® Tape on Myofascial Pain Syndrome of the Iliotibial Band
A NA study of Myofascial Trigger Point Pain, sponsored by North Dakota State University.
- Completed
- Registry status
- NA
- Development phase
- 50
- Enrollment target
- 1
- Study location
NCT04531306: Completed NA study of Myofascial Trigger Point Pain, sponsored by North Dakota State University.
NCT04531306 is a NA study of Myofascial Trigger Point Pain that has completed, run by North Dakota State University. The registered enrollment target is 50 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT04531306, a NA study of Myofascial Trigger Point Pain, has completed, sponsored by North Dakota State University.
- COMPLETED
- Registry status
- NA
- Development phase
- 50 participants
- Enrollment target
- 1
- Study location
Study Summary
Participants will report for two research sessions. Prior to arrival, membership to a club sports team will be confirmed via email. The first session will require one hour, while the second will require 30 minutes. Maximum amount of time expected is one and a half hours, over two sessions in 48 hours. The 1st and 2nd sessions will be separated by 48 hours. Upon arrival for session 1, informed consent will be obtained along with the following demographic information: age, sex, height, weight, dominant leg, and sport. Next, the participant will complete the Musculoskeletal Questionnaire (MQ) in regard to the last 12 months. Participants will then be assessed for trigger points in their dominant side iliotibial band via palpation. Diagnostic criteria for trigger point will be modeled after Travell and Simons: taut band, pain upon palpation, referred pain, and a local twitch response. Up to four trigger points will be marked on the subject's skin with marker or pen. Pain pressure threshold will be obtained via algometer, using the terminology "Tell me the first moment you experience pain by verbalizing 'pain' ". Then, three pain pressure threshold readings will be taken per trigger point and then averaged by the researcher. Kinesiology tape will then be applied to the identified trigger points using the Fascial Technique. Pain pressure threshold will be obtained again with the same protocols 10 minutes after the tape is applied. The participant will be asked to wear the tape for 48 hours. Upon arrival for session 2, the application of the tape will be confirmed. With the participant's choice to continue in the study, a third and fourth measurement of pain pressure threshold will be obtained: one with the tape remaining on, and another 10 minutes after removal of the tape. Again, three pain pressure threshold readings will be taken per trigger point and then averaged by the researcher.
Primary Outcome
measured by pain pressure threshold (N/s2) via algometer
Conditions Studied
Interventions
- OTHER Kinesio® Tape
Study Locations (1)
North Dakota
- North Dakota State University - Fargo
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2020-10-04 |
| Est. Completion | 2020-11-01 |
| Phase | NA |
What the finished NCT04531306 record still lists
NCT04531306 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).
The record links to 1 condition, with Myofascial Trigger Point Pain appearing as the primary indexed condition, and to 1 intervention - of which Kinesio® Tape is the first listed.
NCT04531306 reports a single indexed study location in North Dakota.
Frequently Asked Questions
What is clinical trial NCT04531306 about?
NCT04531306 is a clinical study titled "An Analysis of Kinesio® Tape on Myofascial Pain Syndrome of the Iliotibial Band". Participants will report for two research sessions. Prior to arrival, membership to a club sports team will be confirmed via email. The first session will require one hour, while the second will require 30 minutes. Maximum amount of time expected is one and a half hours, over two sessions in 48 hour...
What is the current status of trial NCT04531306?
This trial is currently completed. It is a NA study. The enrollment target is 50 participants. The study started on 2020-10-04. Estimated completion is 2020-11-01.
What conditions does trial NCT04531306 study?
This clinical trial studies the following conditions: Myofascial Trigger Point Pain.
What interventions are being tested in trial NCT04531306?
The interventions under investigation include: Kinesio® Tape (OTHER).
Who is sponsoring clinical trial NCT04531306?
This trial is sponsored by North Dakota State University, which has 16 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT04531306 being conducted?
This trial has 1 study location across North Dakota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Where NCT04531306's enrollment target sits among peer trials
50 1279th of 2000 higher than 622 of 2,000 other NA trials
participants (enrollment target), bucketed by value
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