search  
 


Home

Who are we?

Why
register?


Signup for
registration


Online registration

Log in to register
your trial


Search a trial

NRT en CCMO

Contact

NEDERLANDS





MetaRegister
van CCT (UK)


ISRCTN-Register
van CCT (UK)


Effect of a six week functional hip strengthening program on running biomechanics in runners with patellofemoral pain


- candidate number22990
- NTR NumberNTR5553
- ISRCTNISRCTN no longer applicable
- Date ISRCTN created
- date ISRCTN requested
- Date Registered NTR22-okt-2015
- Secondary IDsMETc2015/361 M15.178467
- Public TitleEffect of a six week functional hip strengthening program on running biomechanics in runners with patellofemoral pain
- Scientific TitleEffect of a six week functional hip strengthening program on running biomechanics in runners with patellofemoral pain
- ACRONYM
- hypothesis
- Healt Condition(s) or Problem(s) studiedPatellofemoral pain
- Inclusion criteriaMale and female subjects with the following criteria are eligible for inclusion:
1. Anterior or retropatellar kneepain in at least two of the following activities: ascending and descending stairs, hopping, and running, squatting, kneeling and prolonged sitting.
2. Insidious onset of symptoms not related to trauma
3. Pain with compression of the patella
4. Pain on palpation of patellar facets
5. Involvement in at least 30minutes of physical activity 3days a week consisting of at least one time running
- Exclusion criteria1. Symptoms present for less than 2 months
2. Self reported clinical evidence of other knee pathology
3. History of knee surgery
4. Self reported history of patella dislocations or subluxations
5. Current significant injury affection other lower extremity joints
- mec approval receivedyes
- multicenter trialno
- randomisedno
- group[default]
- TypeSingle arm
- Studytypeobservational
- planned startdate 10-nov-2015
- planned closingdate1-okt-2016
- Target number of participants13
- InterventionsPatients receive six sessions of physical therapy with a one week interval. These sessions will consist of a standardized training progressing in difficulty and resistance over time. In between the physical therapy sessions the patients will be performing a home training program three times a week, which progresses in difficulty and resistance over time.
- Primary outcome• Running biomechanics of the knee and hip. Expressed in peak angles of external knee abduction, hip adduction and contralateral pelvicdrop measured with a motion capture system.
• Hip strength. Expressed in KG normalized to the patients’ body composition. Measured with a hand held dynamometer.
- Secondary outcomePain on a Visual Analogue Scale (VAS) in which 0 represents no pain, and 100 maximal pain:
• Directly after running, during measurement of running biomechanics
- Timepoints1. Intake measurement
2. Measurement after a six week training period
3. Follow-up measurement: ten weeks after initial intake
- Trial web siteN/A
- statusplanned
- CONTACT FOR PUBLIC QUERIES Mark Korte
- CONTACT for SCIENTIFIC QUERIES Mark Korte
- Sponsor/Initiator University Medical Center Groningen (UMCG), Avans Plus Hogeschool
- Funding
(Source(s) of Monetary or Material Support)
University Medical Center Groningen (UMCG), AVANS PLus
- PublicationsN/A
- Brief summaryRelevance: Patellofemoral pain is a common diagnose in young adults and adolescents. In running it is the most common knee injury, recorded up to 46%.

In despite of the high prevalence there is not much literature available regarding treatment on the topic. In a couple studies it has been shown that runners with PFP have changed running biomechanics and a strength deficit at the affected side. Currently there is evidence that a hip strengthening program reduces pain. Also there is evidence that gait retraining reduces pain. For the physical therapist it is important to understand what to expect from a particular intervention.

Objective: The aim of this study is to explore the effects of a functional training program for hip strengthening on running biomechanics.

Study design: A pre experimental design study with the number of at least n=13 subjects. An intake measurement will be followed by a six-week training program. A second measurement will take place after the six weeks of training. A follow-up measurement is planned four weeks after the second measurement.
- Main changes (audit trail)
- RECORD22-okt-2015 - 27-feb-2016


  • Indien u gegevens wilt toevoegen of veranderen, kunt u een mail sturen naar nederlands@trialregister.nl