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Behavioural Intervention

Intervention: Knee KG informed physical therapy for Patellofemoral Pain Syndrome

N/A
Waitlist Available
Led By Don L Goss, DPT, PhD
Research Sponsored by Womack Army Medical Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
* Age 18-50
* Active Duty Service Member stationed at Fort Liberty and Schofield Barracks
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 12 weeks
Awards & highlights

Summary

This is a randomized clinical trial investigating the use of the Emovi Knee Kinesiography information in the treatment of anterior knee pain in physical therapy.

Eligible Conditions
  • Patellofemoral Pain Syndrome

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~12 weeks
This trial's timeline: 3 weeks for screening, Varies for treatment, and 12 weeks for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Patient-Reported Outcomes Measurement Information System (PROMIS) Physical Function
Secondary study objectives
Anterior Knee Pain Scale (AKPS)
Patient-Reported Outcomes Measurement Information System (PROMIS) Pain Interference
Provider Satisfaction
+2 more

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Intervention: Knee KG informed physical therapyExperimental Treatment1 Intervention
Participants in this group will receive care guided by the impairments identified with the KneeKG. The KneeKG exam results in recommended exercises that target the specific biomechanical impairments identified. The exercises and dose given to the participant will be based on what the KneeKG device recommends after the exam. The participant will be seen twice a week for 4 weeks.
Group II: Control: Standard of care physical therapyActive Control1 Intervention
Participants in this arm will have their KneeKG data captured, but this information will not be provided to the physical therapist to inform their care. Instead, physical therapists will deliver care as they normally do in routine clinical practice. The participant will be seen twice a week for 4 weeks.

Find a Location

Who is running the clinical trial?

Womack Army Medical CenterLead Sponsor
20 Previous Clinical Trials
16,475 Total Patients Enrolled
Medical Technology Enterprise ConsortiumUNKNOWN
2 Previous Clinical Trials
160 Total Patients Enrolled
The Geneva FoundationOTHER
35 Previous Clinical Trials
12,998 Total Patients Enrolled
~120 spots leftby Oct 2025
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