NCT02924259

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
45

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Sep 2016

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
29 days until next milestone

First Submitted

Initial submission to the registry

September 30, 2016

Completed
5 days until next milestone

First Posted

Study publicly available on registry

October 5, 2016

Completed
27 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2016

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2016

Completed
Last Updated

December 1, 2016

Status Verified

November 1, 2016

Enrollment Period

2 months

First QC Date

September 30, 2016

Last Update Submit

November 30, 2016

Conditions

Keywords

muscle sorenesspainmyofascial release

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

EXPERIMENTAL

Subjects will undergo a 2-minute video-guided foam roll intervention on the left quadriceps muscle using the GRID foam roll.

Device: The GRID foam roll

Interventions

Commercial rigid foam roll with an outer foam covering

Foam Roll Group

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

MeSH Terms

Conditions

Myofascial Pain SyndromesMyalgiaPain

Condition Hierarchy (Ancestors)

Muscular DiseasesMusculoskeletal DiseasesNeuromuscular DiseasesNervous System DiseasesMusculoskeletal PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Scott W Cheatham, PhD, DPT

    CSUDH

    PRINCIPAL INVESTIGATOR

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

Locations