Does Self-myofascial Release With a Foam Roll Change Pressure Pain Thresholds in Lower Extremity Muscles
1 other identifier
interventional
45
1 country
1
Brief Summary
The purpose of this study was to examine the effects of a foam rolling intervention on pressure pain thresholds (PPT) of the ipsilateral antagonist and contralateral muscle groups. Through this research we sought to gather data to further develop the methodology for future studies of this intervention.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Sep 2016
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 1, 2016
CompletedFirst Submitted
Initial submission to the registry
September 30, 2016
CompletedFirst Posted
Study publicly available on registry
October 5, 2016
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 1, 2016
CompletedStudy Completion
Last participant's last visit for all outcomes
November 1, 2016
CompletedDecember 1, 2016
November 1, 2016
2 months
September 30, 2016
November 30, 2016
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change from baseline pressure pain threshold to immediate post intervention.
Pressure pain threshold will be tested immediately before the intervention and immediately after the intervention on the left hamstring and right quadriceps muscle groups.
baseline and immediately post intervention
Study Arms (1)
Foam Roll Group
EXPERIMENTALSubjects will undergo a 2-minute video-guided foam roll intervention on the left quadriceps muscle using the GRID foam roll.
Interventions
Eligibility Criteria
You may qualify if:
- Healthy adults
You may not qualify if:
- Musculoskeletal, systemic, or metabolic disease that would affect lower extremity joint ROM or tolerance to pressure pain threshold testing and the inability to avoid medications that may affect testing.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Cal State University Dominguez Hills
Carson, California, 90747, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Scott W Cheatham, PhD, DPT
CSUDH
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
September 30, 2016
First Posted
October 5, 2016
Study Start
September 1, 2016
Primary Completion
November 1, 2016
Study Completion
November 1, 2016
Last Updated
December 1, 2016
Record last verified: 2016-11
Data Sharing
- IPD Sharing
- Will not share