NCT06974409

Brief Summary

This study is a within-subject controlled trial . The investigators will compare unilateral force production in a bodyweight double-leg squat before and after a standardized foam rolling session with the use of Vald ForceDecks. TheForceDecks use sensors embedded within separate plates to record the forces exerted. Participants will have their weight, height, and dorsiflexion range of motion measured prior to performing 3 double-leg squats. Participants will then be instructed on the foam rolling technique. They will perform the technique on each quadriceps group and will state their pain level at 30 seconds and at 2 minutes using the VAS pain scale.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
21

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jun 2025

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

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

May 7, 2025

Completed
8 days until next milestone

First Posted

Study publicly available on registry

May 15, 2025

Completed
27 days until next milestone

Study Start

First participant enrolled

June 11, 2025

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 18, 2025

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

September 30, 2025

Completed
Last Updated

January 12, 2026

Status Verified

January 1, 2026

Enrollment Period

2 months

First QC Date

May 7, 2025

Last Update Submit

January 8, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • Force Production

    Unilateral lower extremity force production during a single-leg squat.

    30 minutes

Study Arms (1)

Foam Rolling Regime

EXPERIMENTAL

2-minute quadriceps foam rolling regime

Device: foam roller

Interventions

foam rollers with grids, knobs, and spikes

Foam Rolling Regime

Eligibility Criteria

Age18 Years - 22 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Redlands

Redlands, California, 92373, United States

Location

Related Publications (6)

  • Hendricks S, Hill H, Hollander SD, Lombard W, Parker R. Effects of foam rolling on performance and recovery: A systematic review of the literature to guide practitioners on the use of foam rolling. J Bodyw Mov Ther. 2020 Apr;24(2):151-174. doi: 10.1016/j.jbmt.2019.10.019. Epub 2019 Nov 2.

    PMID: 32507141BACKGROUND
  • Plisky PJ, Bullock GS, Garner MB, Ricard R, Hayden J, Huebner B, Schwartzkopf-Phifer K, Kiesel K. The Dorsiflexion Range of Motion Screen: A Validation Study. Int J Sports Phys Ther. 2021 Apr 1;16(2):306-311. doi: 10.26603/001c.21253.

    PMID: 33842026BACKGROUND
  • Pardo E, El Behi H, Boizeau P, Verdonk F, Alberti C, Lescot T. Reliability of ultrasound measurements of quadriceps muscle thickness in critically ill patients. BMC Anesthesiol. 2018 Dec 27;18(1):205. doi: 10.1186/s12871-018-0647-9.

    PMID: 30591032BACKGROUND
  • Michalak B, Kopiczko A, Gajda R, Adamczyk JG. Recovery effect of self-myofascial release treatment using different type of a foam rollers. Sci Rep. 2024 Jul 9;14(1):15762. doi: 10.1038/s41598-024-66577-x.

    PMID: 38982124BACKGROUND
  • Junker D, Stoggl T. The Training Effects of Foam Rolling on Core Strength Endurance, Balance, Muscle Performance and Range of Motion: A Randomized Controlled Trial. J Sports Sci Med. 2019 Jun 1;18(2):229-238. eCollection 2019 Jun.

    PMID: 31191092BACKGROUND
  • Healey KC, Hatfield DL, Blanpied P, Dorfman LR, Riebe D. The effects of myofascial release with foam rolling on performance. J Strength Cond Res. 2014 Jan;28(1):61-8. doi: 10.1519/JSC.0b013e3182956569.

    PMID: 23588488BACKGROUND

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
PREVENTION
Intervention Model
SINGLE GROUP
Model Details: Single Group Assessment .
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Doctor

Study Record Dates

First Submitted

May 7, 2025

First Posted

May 15, 2025

Study Start

June 11, 2025

Primary Completion

August 18, 2025

Study Completion

September 30, 2025

Last Updated

January 12, 2026

Record last verified: 2026-01

Data Sharing

IPD Sharing
Will not share

IPD will only be used for this particular study.

Locations