Patellofemoral Pain Syndrome Clinical Trial
Official title:
The Use of Wii Fit ™ to Increase Compliance With Home Exercises for Treatment of Patellofemoral Syndrome in Adolescent Females
Verified date | June 2010 |
Source | University of Manitoba |
Contact | n/a |
Is FDA regulated | No |
Health authority | Canada: Ethics Review Committee |
Study type | Interventional |
To determine the utility of the Wii Fit TM interactive video game program in patellofemoral symptom resolution, development of increased muscle strength and flexibility as a result of increased compliance with home exercises in adolescent females with patellofemoral syndrome.
Status | Terminated |
Enrollment | 22 |
Est. completion date | September 2010 |
Est. primary completion date | September 2010 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 11 Years to 17 Years |
Eligibility |
Inclusion Criteria: - Female between ages of 11 and 17 years of age - A diagnosis of patellofemoral syndrome with one or more of the following symptoms: anterior knee pain, positive theater sign, stairs provoking knee pain. - No physiotherapy or regular, structured home exercise program is being followed - Parental/guardian consent to participate - Patient assent to participate Exclusion Criteria: - Patients participating in physiotherapy at the time of initial assessment or have had physiotherapy in the last 6 months for patellofemoral syndrome - Patients performing regular home exercise program prescribed by physician, physiotherapist, or other allied health professional for patellofemoral syndrome at time of initial assessment - Patients who have additional knee pathology (e.g. acute patellar dislocation; acute internal knee derangement (i.e. meniscal, ligament injury); osteochondritis dissecans; severe apophysitis or tendinitis) that could interfere with rehabilitation exercises due to pain or instability from these conditions - Individuals with history of knee surgery - Individuals that have a Wii Fit TM video game at home - Individuals for whom consent and assent is not obtained |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Canada | Legacy Sport Medicine | Winnipeg | Manitoba |
Lead Sponsor | Collaborator |
---|---|
University of Manitoba |
Canada,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Percentage of Exercise Days Completed. | Calculated for the 12 week period as daily exercise completion rate as percentage | 3 months | No |
Secondary | Changes in Patellofemoral Symptoms | 3 months | No | |
Secondary | Change in Hamstring Flexibility | 3 months | No | |
Secondary | Change in Quadriceps Flexibility | 3 months | No | |
Secondary | Change in Vastus Medialis Oblique Muscle Strength | 3 months | No |
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