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| Sponsor: | Cleveland Chiropractic College |
|---|---|
| Information provided by: | Cleveland Chiropractic College |
| ClinicalTrials.gov Identifier: | NCT00401050 |
Purpose
The purpose of this study is to compare outcomes of combined chiropractic care in anterior knee pain patients with patellofemoral pain syndrome.
| Condition | Intervention |
|---|---|
|
Patellofemoral Pain Syndrome |
Procedure: chiropractic manipulative therapy Procedure: knee exercises Procedure: Graston Instrument Soft Tissue Mobilization (GISTM) |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Single Blind (Outcomes Assessor) Primary Purpose: Treatment |
| Official Title: | A Randomized Clinical Trial Comparing Two Chiropractic Protocols for Patellofemoral Pain Syndrome: a Pilot Study |
| Enrollment: | 31 |
| Study Start Date: | June 2006 |
| Study Completion Date: | December 2007 |
| Primary Completion Date: | December 2007 (Final data collection date for primary outcome measure) |
Exercise is standard of care for PFPS but gives limited pain reduction and functional improvement. Previous manipulative therapy for PFPS (with and without exercise) has been limited to the patellofemoral joint alone. However, literature suggests additional manipulative therapy with exercise and soft-tissue treatment may give a better outcome. Further research is needed.
Therefore, this project is a pilot study to inform a future randomized controlled trial to determine if chiropractic adjusting of the full lower extremity (lumbosacral through foot) combined with exercise and soft tissue treatment (Protocol and group A) is superior to chiropractic adjusting of the knee (alone) combined with exercise and soft tissue treatment (Protocol and group B) in the treatment of patellofemoral pain syndrome. We will use the Anterior Knee Pain Scale (AKPS) and Visual Analogue Scale (VAS) as valid and reliable primary outcome measures, a functional measure (step-ups, step-downs and squats) and a Patient Satisfaction Scale (PSS - discharge or refer) as secondary outcome measures. This study will help establish the feasibility of conducting quality research at Cleveland Chiropractic College Los Angeles.
In this pilot study there will be two groups of 10 subjects each
Enrolled subjects will receive a total of 6 treatments. The primary endpoint will be a 2 month follow-up after the 6th treatment.
Eligibility| Ages Eligible for Study: | 18 Years to 45 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| United States, California | |
| Cleveland Chirpractic College Los Angeles | |
| Los Angeles, California, United States, 90004 | |
| Principal Investigator: | James W. Brantingham, D.C., PhD. | Cleveland Chiropractic College Los Angeles |
More Information
| Responsible Party: | James W. Brantingham, DC, PhD, Cleveland Chiropractic College |
| ClinicalTrials.gov Identifier: | NCT00401050 History of Changes |
| Other Study ID Numbers: | 06-15-06 |
| Study First Received: | November 16, 2006 |
| Last Updated: | April 16, 2010 |
| Health Authority: | United States: Institutional Review Board |
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patellofemoral pain syndrome chiropractic knee pain chiropractic manipulation Graston Instrument Soft Tissue Mobilization(GISTM) |
|
Somatoform Disorders Patellofemoral Pain Syndrome Mental Disorders Joint Diseases Musculoskeletal Diseases |