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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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28 November 2016 |
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Main ID: |
NCT02674841 |
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Date of registration:
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01/02/2016 |
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Prospective Registration:
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Yes |
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Primary sponsor: |
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Public title:
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Live Feedback to Increase Adherence in Adolescents With Patellofemoral Pain
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Scientific title:
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Efficacy of Live Feedback to Increase Objectively Monitored Adherence to Prescribed, Home-based, Exercise Therapy-dosage in 15 to 19 Year Old Adolescents With Patellofemoral Pain. A Randomized Controlled Superiority Trial |
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Date of first enrolment:
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February 2016 |
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Target sample size:
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40 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT02674841 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment
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Phase:
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N/A
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Countries of recruitment
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Denmark
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Contacts
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Name:
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Michael S Rathleff, Ph.d. |
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Address:
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Telephone:
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Email:
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Affiliation:
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Aalborg University |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- 15 to 19 years of age
- Anterior knee pain of non-traumatic origin which is provoked by at least two of the
following activities: prolonged sitting with bended knees or kneeling, squatting,
running, jumping or ascending or descending stairs
- Tenderness on palpation of the peripatellar borders
- Pain of more than 6 weeks duration
- Worst pain during the previous week = 30 mm on a 100 mm VAS
Exclusion Criteria:
- Concomitant pain from other structures in the knee (e.g. ligament, tendon or
cartilage), the hip or the lumbar spine
- Previous knee surgery
- Patellofemoral instability
Age minimum:
15 Years
Age maximum:
19 Years
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Joint Diseases
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Musculoskeletal Disorders
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Patellofemoral Pain Syndrome
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Intervention(s)
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Other: No feedback on TUT
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Other: Feedback on TUT
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Other: Exercise
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Primary Outcome(s)
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Mean deviation from the prescribed TUT per repetition in seconds during the course of the intervention
[Time Frame: From 0-6 weeks]
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Secondary Outcome(s)
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Global rating of change
[Time Frame: At the 6 week follow up]
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Kujala Patellofemoral Scale-score
[Time Frame: At baseline and at the 6 week follow up]
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Isometric strength
[Time Frame: At baseline and at the 6 week follow up]
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Summary of resistance
[Time Frame: From 0-6 weeks]
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Pulling force exerted per repetition measured in kilos
[Time Frame: From 0-6 weeks]
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Pain measured on a 100 mm VAS
[Time Frame: From 0-6 weeks]
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The total number of repetitions performed
[Time Frame: From 0-6 weeks]
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Secondary ID(s)
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N-20150070
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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