ClinicalTrials.Veeva

Menu

This Study Will Compare Force Production in Double-leg Squats of College Students Before and After a Standardized Foam Rolling Session

U

University of Redlands

Status

Completed

Conditions

Force Production
Pain Intensity Assessment

Treatments

Device: foam roller

Study type

Interventional

Funder types

Other

Identifiers

NCT06974409
Protocol #2025-003-Redlands

Details and patient eligibility

About

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.

Full description

The invetigators will compare independent bilateral double-leg squat force productions before and after a structured foam rolling routine. Participants will first be measured for height, weight, and dorsiflexion ROM (SADS; standing ankle dorsiflexion screen). Quadriceps muscle belly length will be determined by measuring from the ASIS to the superior pole of the patella and marking the middle 2/3 of the region. Participants will then stand on VALD ForceDecks for normalization. (The ForceDecks use sensors embedded within separate plates to record the forces exerted by each leg.) With hands on hips, participants will perform three body weight double leg squats (squatting above 90 degrees of knee flexion). Participants will then watch a demonstration of single leg quadriceps foam rolling which will consist of 3-point contact in a plank position with the targeted leg not having contact with the ground. Participants will be cued for continuous motion on a count of 3 seconds in each direction without pausing. Participants will be asked to respond to a visual analog scale for pain at 30 seconds and at 2 minutes (end of session). Participants will be given a 30-second rest between sides. Upon completion, participants will return to the ForceDecks and perform 3 additional body weight double-leg squats with hands on hips (approximate same depth of squat as the initial set).

Enrollment

21 patients

Sex

All

Ages

18 to 22 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria: university student; 18-22 years of age -

Exclusion Criteria: unable to get up from the ground without assistance; current lower extremity injury; prior lower extremity surgery in the past 10 years

-

Trial design

Primary purpose

Prevention

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

21 participants in 1 patient group

Foam Rolling Regime
Experimental group
Description:
2-minute quadriceps foam rolling regime
Treatment:
Device: foam roller

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems