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NCT06234202 Clinical Trial

The Effect of a Bioactive Fabric Sleeve

Recovery Clinical Trial

Official title:
The Effect of a Bioactive Fabric Sleeve on Recovery in Division I Collegiate Baseball Players

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT06234202
Other study ID # 72979
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date February 2024
Est. completion date June 2024

Study information
Verified date January 2024
Source Stanford University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In-season pitch volume have been shown to relate to arm soreness in collegiate baseball players. Arm soreness is a common ailment following a pitching appearance due to the adaptation to soft tissue in response to a repetitive load to the throwing arm. Specifically, ongoing and accumulated fatigue and soreness to the flexor pronator mass region of the arm may be a predecessor for UCL injury. Different recovery modalities such as a bioactive fabric sleeve may give pitchers a recovery advantage throughout a baseball season. The primary purpose of this study is to determine if there is a difference in subjective soreness of the flexor pronator mass the day following a game pitching appearance using a sleeve with bioactive fabric which potentially improves cellular function versus a control sleeve.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 17
Est. completion date June 2024
Est. primary completion date June 2024
Accepts healthy volunteers No
Gender Male
Age group 18 Years and older
Eligibility Inclusion Criteria: - Stanford Baseball Player Exclusion Criteria: - None

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• Bioactive Sleeve
Pitchers will wear a bioactive sleeve immediately post-game through overnight.
• Control Sleeve
Pitchers will wear a non-bioactive sleeve immediately post-game through overnight.

Locations
Country Name City State
United States Stanford University Stanford California

Sponsors (2)
Lead Sponsor Collaborator
Stanford University Challenger Health, LLC

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Subjective Soreness Score Subjective soreness questionnaires to rank soreness, tightness, and discomfort of the medial forearm on a 1 to 10 scale will be collected throughout the baseball seasons. Baseline through 6 months
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