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Ankle Mobilization for Knee Pain
N/A
Recruiting
Led By Everett Lohman, Dsc
Research Sponsored by Loma Linda University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up change between baseline and post intervention on day 1
Awards & highlights
No Placebo-Only Group
Summary
This trial aims to see if improving ankle movement can help people with knee pain perform squats better. Participants will do exercises to increase ankle flexibility and then test their knee function.
Who is the study for?
This trial is for women aged 18-59 with Patellofemoral Pain lasting at least 6 months, who haven't had clinic treatments in that time. They must have limited ankle movement (<45 degrees on a lunge test) and no knee swelling, abnormal limb structures, severe resting pain, or past surgery/fractures affecting leg/spine biomechanics.
What is being tested?
The study examines how limited ankle flexibility affects single-leg squats in those with knee pain. Participants will either receive 'Mobilization with Movement' therapy or just education without mobilization to see which method better improves squat performance.
What are the potential side effects?
Since the interventions involve physical therapy techniques and educational components rather than medication, side effects are minimal but may include temporary discomfort or muscle soreness from the movements performed during the sessions.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ change between baseline and post intervention on day 1
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~change between baseline and post intervention on day 1
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Weight bearing lunge test
Secondary study objectives
Patellofemoral Disability Index
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Primary Intervention GroupExperimental Treatment1 Intervention
The experimental group will receive two interventions to increase dorsiflexion range of motion.
Group II: Minimal Intervention GroupActive Control1 Intervention
The minimal intervention group will read and infographic and complete 5 minutes of treadmill walking.
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
The most common treatments for Patellofemoral Pain Syndrome (PFPS) focus on biomechanical corrections through physical therapy exercises, orthotic devices, and taping techniques. Physical therapy aims to strengthen the quadriceps, improve hip and core stability, and enhance flexibility in the hamstrings and calf muscles, which helps correct patellar tracking and reduce knee joint stress.
Orthotic devices and taping improve foot alignment and reduce abnormal forces on the knee. These treatments are essential for PFPS patients as they address the underlying biomechanical issues, leading to more effective and sustained pain relief.
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Who is running the clinical trial?
Loma Linda UniversityLead Sponsor
316 Previous Clinical Trials
266,641 Total Patients Enrolled
1 Trials studying Patellofemoral Pain Syndrome
43 Patients Enrolled for Patellofemoral Pain Syndrome
Everett Lohman, DscPrincipal InvestigatorLoma Linda University
2 Previous Clinical Trials
79 Total Patients Enrolled
1 Trials studying Patellofemoral Pain Syndrome
43 Patients Enrolled for Patellofemoral Pain Syndrome
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- You have had bone or muscle problems in the limb being tested before.You have severe pain at rest, rated greater than 5 out of 10.You have had surgery or fractures in your leg or lower back that could affect the way you move during the study.You have difficulty moving your foot upwards when standing, as detected by a test called weight bearing lunge test, where you are required to bend your knee and tilt your body forward.
Research Study Groups:
This trial has the following groups:- Group 1: Minimal Intervention Group
- Group 2: Primary Intervention Group
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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