ClinicalTrials.gov
ClinicalTrials.gov Menu

Hip Strengthening Versus Quadriceps Based Training for Patellofemoral Pain Syndrome

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT02114294
Recruitment Status : Unknown
Verified April 2014 by Sorlandet Hospital HF.
Recruitment status was:  Recruiting
First Posted : April 15, 2014
Last Update Posted : March 5, 2015
Sponsor:
Information provided by (Responsible Party):
Sorlandet Hospital HF

Brief Summary:
This is a Randomized Controlled Trial (RCT) regarding conservative treatment of Patellofemoral Pain Syndrome (PFPS). Patellofemoral Pain Syndrome (PFPS) is a very common cause of knee pain in young active adults with a high rate of recurrent and/or chronic occurrence. PFPS is notoriously difficult to treat and has been referred to as "one of the most vexatious clinical challenges in rehabilitative medicine". Its etiology is unclear but is commonly thought to be related to pathomechanics in the patellofemoral joint (PFJ). There are many factors that can influence PFJ mechanics. Among these, quadriceps strength and timing has been shown to be important. As such, treatment of PFPS has traditionally been based on correction of pathomechanics through influencing quadriceps strength and timing. However, a growing body of evidence is revealing the importance of strength and control of hip abduction and external rotation in PFPS. Hip strength in ab/adduction and rotation is thought to influence femoral positioning in the patellofemoral joint, thereby affecting PFJ mechanics. Several cohort and smaller RCT studies within the last 7 years have shown that additional exercises for hip strength and control give an improved effect in pain and function compared with quadriceps based training alone. A smaller RCT from 2012 compared isolated hip strengthening exercises to a control group and found surprisingly good results on pain in function in the hip strengthening group. The investigators plan a RCT in which isolated hip strengthening will be compared to traditional quadriceps training and a control group which will receive no structured training. Primary outcomes will be pain and function. This high-quality study will include 40-50 patients in each group, making it one of the largest of its kind on conservative treatment for PFPS. In contrast to the vast majority of studies of this type, this study will also include men, which will potentially help to fill a significant gap in the literature on this subject. The investigators study will therefore be an important contribution to elucidating the etiology of PFPS and improving treatment options for both men and women in the future. As well, the role of psychometric parameters will be examined and a standardized clinical test for hip abduction endurance will be developed.

Condition or disease Intervention/treatment Phase
Patellofemoral Pain Syndrome Other: Isolated hip strengthening Other: Quadriceps based training Other: Active control Not Applicable

Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 150 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double (Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Official Title: Does Isolated Hip Strengthening for Patellofemoral Pain Syndrome Give Better Long Term Results Than Traditional Quadriceps Based Training? A Randomised Controlled Trial.
Study Start Date : October 2014
Estimated Primary Completion Date : May 2017
Estimated Study Completion Date : May 2018

Arm Intervention/treatment
Experimental: Isolated hip strengthening
Isolated hip strengthening (abduction, external rotation, extension)
Other: Isolated hip strengthening
Exercise program that is carried out by subjects under supervision once a week and then performed at home 2 additional times without supervision for a total of 6 weeks. Hip strengthening group will train hip abduction, hip external rotation and hip extension.

Active Comparator: Quadriceps based training
Quadriceps based training (mini-squat, straight leg raising, terminal extensions)
Other: Quadriceps based training
Exercise program that is carried out by subjects under supervision once a week and then performed at home 2 additional times without supervision for a total of 6 weeks. Quadriceps group will train mini-squat, straight leg raising, terminal extensions.

Active control
Patients receive standardised information concerning patellofemoral pain syndrome, but receive no prescribed exercise regime. They are encouraged to remain active.
Other: Active control
Patients receive standardised information concerning patellofemoral pain syndrome, but receive no prescribed exercise regime. They are encouraged to remain active.




Primary Outcome Measures :
  1. Anterior knee pain score [ Time Frame: 3 months ]
    Anterior Knee Pain Score (AKPS) is a measurement of subjective symptoms and functional limitations in patellofemoral pain, and has been validated for use in this patient population. The AKPS consists of a 13-point questionnaire with categories related to different levels of function in the knee. The categories within each question are weighted, and the responses are summed for an overall index where 100 represents perfect function. The mean clinically important difference (MCID) has been determined to be 10 points. This questionnaire will be translated to Norwegian and validated according to standard scientific procedures with approval from Kuala et al.


Secondary Outcome Measures :
  1. Visual Analog Scale (VAS) [ Time Frame: 3 months ]
    Visual Analog Scale (VAS) for pain (0-10cm)

  2. Global Score Global Score [ Time Frame: 3 months ]
    An 18-point likert scale for measuring patients' global assessment of change compared with baseline will be carried out at 3 and 12 months. The scale ranges from -9 (maximum deterioration) to +9 (maximum improvement).

  3. Step-down test [ Time Frame: 3 months ]
    The step down as performed according to standardised instruction will be used to quantify changes in patients' function. The measure is number of repetitions in 30 seconds.

  4. Hip abduction, external rotation and knee extension strength [ Time Frame: 3 months ]
    Isometric strength will be measured for hip abduction, hip external rotation and knee extension.

  5. Hip abduction endurance [ Time Frame: 3 months ]
    Testing is carried out in side-lying position with a 5kg weight around the ankle of the upper leg, which is abducted to 30 degrees above the horizontal plane. Time successfully held in target area is measured in seconds.

  6. EQ 5D 5L [ Time Frame: 3 months ]
    EQ-5D-5L is calculated on the basis of five questions about daily activities, pain and psychological status with five possible answers for each question. In addition the subject scores his/her overall health on a 1-100 scale. The results are translated to a single summary index value through the use of a table

  7. Tampa scale for kinesiophobia [ Time Frame: 3 months ]
    The Tampa scale for kinesiophobia (TSK) is a 13 -item questionnaire aimed at the assessment of fear of movement/re-injury. Each item is scored on a 4-point Likert scale with alternatives ranging from "strongly disagree" (0) to "strongly agree". This gives a possible total score range from 0 to 52.

  8. HSCL-10 [ Time Frame: 3 months ]
    The Hopkins Symptom Checklist (HSCL) is a symptom inventory which measures symptoms of anxiety and depression.

  9. Knee self-efficacy score (K-SES) [ Time Frame: 3 months ]
    K-SES is a self-administered instrument consisting of in total four sections in which patients score how certain they are about specific activities currently and in the future.

  10. Pain drawing with number of painful regions [ Time Frame: 3 months ]
    An adaptation of the Standardised Nordic Questionnaire will be used to register the number of painful areas.



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   16 Years to 40 Years   (Child, Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Age 16-40 years
  • Insidious onset of symptoms not related to trauma
  • Symptoms more than 3 months
  • A minimum of VAS 3 on VAS-W
  • Peri- or retropatellar pain during or after at least two of the following: Stair ascent or descent, hopping, running, prolonged sitting, squatting, kneeling.
  • Pain on one of the following: Compression of the patella, palpation of the patellar facets

Exclusion Criteria:

  • Clinical findings indicative of meniscal or other intraarticular injury
  • Clinical findings indicative of injury to or increased laxity of cruciate or collateral ligaments
  • Findings on MRI indicative of other intraarticular pathology.
  • Clinical and/or x-ray findings (plain anterior-posterior, lateral and skyline view) indicative of osteoarthritis, Osgood-Schlatter or Sinding-Larsen-Johanssen syndrome
  • Clinical findings indicative of knee joint effusion
  • Significant pain from hip or lumbar spine on clinical evaluation, with potential for causing referred pain to the knee or hindering the patient's ability to perform the prescribed exercises.
  • Recurrent patellar subluxation or dislocation.
  • Previous surgery to the knee joint
  • NSAID or cortisone use over an extended period of time
  • Having suffered trauma to the knee joint judged during clinical evaluation to have a significant effect on the presenting clinical condition.
  • Physiotherapy or other similar treatment for patellofemoral pain syndrome within the previous 3 months

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02114294


Contacts
Contact: Alexandra C Hott, MD +4738149300 alexandra.hott@sshf.no
Contact: Sigurd Liavaag, MD, PhD +4737014000 sigurd.liavaag@sshf.no

Locations
Norway
Sorlandet hospital Recruiting
Kristiansand, Vest Agder, Norway, 4633
Principal Investigator: Alexandra C Hott, MD         
Sub-Investigator: Sigurd Liavaag, MD, PhD         
Sponsors and Collaborators
Sorlandet Hospital HF
Investigators
Study Director: Sigurd Liavaag, MD, PhD Sørlandet sykehus HF
Principal Investigator: Alexandra C Hott, MD Sørlandet sykehus HF

Publications:

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: Sorlandet Hospital HF
ClinicalTrials.gov Identifier: NCT02114294     History of Changes
Other Study ID Numbers: 2013/1860REK
First Posted: April 15, 2014    Key Record Dates
Last Update Posted: March 5, 2015
Last Verified: April 2014

Keywords provided by Sorlandet Hospital HF:
Patellofemoral pain syndrome
Anterior knee pain
Randomised controlled trial
Exercise intervention
Hip strengthening
Quadriceps based training
Anterior knee pain score

Additional relevant MeSH terms:
Syndrome
Somatoform Disorders
Patellofemoral Pain Syndrome
Disease
Pathologic Processes
Mental Disorders
Joint Diseases
Musculoskeletal Diseases