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NCT06815367 · ClinicalTrials.gov registry record · NA
Pneumatic Compression vs Blood Flow Restriction for Muscle Recovery
A NA study of Delayed Onset Muscle Soreness, sponsored by University of Southern California.
- Recruiting
- Registry status
- NA
- Development phase
- 33
- Enrollment target
- 1
- Study location
NCT06815367 is a NA study of Delayed Onset Muscle Soreness that is actively recruiting participants, run by University of Southern California. The registered enrollment target is 33 participants, below the 40-participant average among 3 other Delayed Onset Muscle Soreness trials with a reported enrollment target (17% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06815367, a NA study of Delayed Onset Muscle Soreness, is actively recruiting participants, sponsored by University of Southern California.
- RECRUITING
- Registry status
- NA
- Development phase
- 33 participants
- Enrollment target
- 1
- Study location
Study Summary
Both BFR and intermittent pneumatic compression are purported to decrease symptoms associated with exercise induced muscle damage (EIMD) that cause delayed onset muscle soreness (DOMS). Blood flow restriction relies on applying pressurized cuffs to the most proximal portion of the limb. Another form of recovery often relied upon is pneumatic compression. The mechanism by which pneumatic compression works is similar to that of a massage, whereby the device progressively increases the pressure on a portion of the limb before releasing and moving further up the limb.The purpose of this study is determine whether BFR or pneumatic compression can be used to decreased DOMS which may indicate enhanced recovery.
Conditions Studied
Interventions
- DEVICE Pneumatic Compression
- DEVICE Blood Flow Restriction
Study Locations (1)
California
- University of Southern California - Los Angeles
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 33 participants |
| Start Date | 2024-01-15 |
| Est. Completion | 2025-12-01 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06815367
The ClinicalTrials.gov registry entry for NCT06815367 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 33 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 40-participant average among 3 other Delayed Onset Muscle Soreness trials with a reported enrollment target (17% lower). The listed sponsor is University of Southern California, which has 617 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Delayed Onset Muscle Soreness appearing as the primary indexed condition, and to 2 interventions - of which Pneumatic Compression is the first listed.
NCT06815367 reports 1 study location spanning 1 distinct geographic area - top geographies include California.
Frequently Asked Questions
What is clinical trial NCT06815367 about?
NCT06815367 is a clinical study titled "Pneumatic Compression vs Blood Flow Restriction for Muscle Recovery". Both BFR and intermittent pneumatic compression are purported to decrease symptoms associated with exercise induced muscle damage (EIMD) that cause delayed onset muscle soreness (DOMS). Blood flow restriction relies on applying pressurized cuffs to the most proximal portion of the limb. Another form...
What is the current status of trial NCT06815367?
This trial is currently recruiting. It is a NA study. The enrollment target is 33 participants. The study started on 2024-01-15. Estimated completion is 2025-12-01.
What conditions does trial NCT06815367 study?
This clinical trial studies the following conditions: Delayed Onset Muscle Soreness.
What interventions are being tested in trial NCT06815367?
The interventions under investigation include: Pneumatic Compression (DEVICE), Blood Flow Restriction (DEVICE).
Who is sponsoring clinical trial NCT06815367?
This trial is sponsored by University of Southern California, which has 617 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06815367 being conducted?
This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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