Lumbar Thrust-mobilization Effects on Hip Strength & Anterior Knee Pain

Status Not yet recruiting

Clinical Trial Summary

The purpose of this study is to investigate changes in lateral hip muscle strength as well as self-reported pain during the performance of three functional tests in patients with anterior knee pain following a lumbopelvic thrust-mobilization.

Hypothesis(es):

Lumbar thrust-mobilization will lead to increased lateral hip strength and decreased anterior knee pain during 3 functional activities (single leg step down, functional squat, drop jump).

Clinical Trial Description

The participant will complete a medical history form and undergo a brief physical exam of the lumbar spine and knees to include: lumbar range of motion and mobility testing, knee range of motion, palpation, and knee mobility testing. The participant will complete a hip strength test utilizing the Biodex System 4 Pro®. The participant will then perform three activities (single leg step down, squat, and drop jump from a 2 foot platform) and provide a self-reported knee pain measure with each activity. A sealed envelope indicating the intervention to be received will be given to the participant. An investigator blinded to the pre and post-measures will open the envelope indicating the intervention to be performed. The participant will be blinded to which intervention group they are categorized to. Th e participant will be positioned on a high-low treatment table to receive the assigned intervention. The participant will be positioned to receive either intervention 1 (thrust mobilization) or 2 (sham mobilization). The participant will either receive the thrust-mobilization or sham mobilization up to 2 times on the left and right side. An immediate re-test of hip strength will be conducted followed by performing the same three functional activities (single leg step down, squat, and drop jump from a 2 foot platform) while providing a self-reported pain measure after each activity. Follow-up measures at 15 minutes post-intervention and the final measure at 30 minutes post-intervention will be performed. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04119310
Study type	Interventional
Source	Messiah College
Contact	Karl Bergmann, PT, ScD
Phone	717-796-1800
Email	kbergmann@messiah.edu
Status	Not yet recruiting
Phase	N/A
Start date	November 1, 2019
Completion date	May 31, 2020

View Details

See also
Status	Clinical Trial	Phase
Completed	`NCT02243332` - Dynamic Quadriceps Muscle Stimulation for Treatment of Patellofemoral Pain	N/A
Completed	`NCT01434966` - Changes in Quadriceps Function Following Local or Distant Interventions in Individuals With Patellofemoral Pain	N/A
Completed	`NCT02750072` - INfrapatellar Versus SUprapatellar Reamed Intramedullary Nailing for Fractures of the Tibia	N/A
Terminated	`NCT01007643` - Use of Wii Fit (TM) to Increase Compliance With Home Exercises in Treating Patellofemoral Syndrome	N/A
Not yet recruiting	`NCT05576064` - Is Gait Analysis for Proposed Rotational Deformities a Useful Resource
Recruiting	`NCT04989023` - Clinical Applications of Blood Flow Restriction and Rehabilitation Outcomes	N/A
Completed	`NCT05778539` - Lateral Retinacular Release in Total Knee Arthroplasty With Patellar Replacement	N/A
Recruiting	`NCT06241053` - Effects of Multimodal Physical Therapy With and Without McConnell Taping in Patients With Anterior Knee Pain.	N/A
Completed	`NCT05055284` - Efficacy of Patellar Taping and Electromyographic Biofeedback Training at Various Knee Angles on Quadriceps Strength and Functional Performance in Patellofemoral Pain Syndrome	N/A
Withdrawn	`NCT00246558` - Tight Achilles Tendon, Hyperpronation and Anterior Knee Pains	N/A
Enrolling by invitation	`NCT05629754` - 10-year Follow-up After Tibial Tubercle Transposition
Terminated	`NCT05617911` - Clinical Comparison of Patellofemoral Pain Syndrome Outcomes After Blood Flow Restriction Therapy	N/A
Completed	`NCT05221060` - Urdu Version of Kujala Questionnaire: A Reliability and Validity Study
Completed	`NCT04752501` - Maladaptive Psychosocial Beliefs and Adolescents With Patellofemoral Pain	N/A
Completed	`NCT03101956` - Lumbar Manipulation for Hip and Muscle Strength	N/A
Completed	`NCT02845869` - Evaluating Light Therapy for Treatment of Overuse Anterior Knee Pain	N/A
Completed	`NCT03615976` - Does Arthroscopic Patellar Denervation With High Tibial Osteotomy Improve Anterior Knee Pain	N/A
Recruiting	`NCT05917080` - Efficacy of Neuromuscular Training and Manual Therapy With Augmented Low-Dye Taping Technique for Correction of Pronated Foot in the Management of Anterior Knee Pain	N/A
Completed	`NCT04134611` - Use of Hyaluronic Acid Injection in Lateral Patellar Compression With Femoral Condylar Degenerative Changes After Arthroscopic Release	N/A
Completed	`NCT06271811` - Flossing Band Integration in Conventional Physiotherapy for Patellofemoral Pain Syndrome	N/A

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

Lumbar Thrust-mobilization Effects on Hip Strength and Anterior Knee Pain

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms