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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04650997
Other study ID # HSEARS20110215003
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 16, 2011
Est. completion date January 1, 2014

Study information

Verified date February 2011
Source The Hong Kong Polytechnic University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Patellar tendinopathy is one of the most common injuries in jumping athletes. Changes in mechanical and physiological properties of tendon are the two proposed forms of pathogenesis. The efficacy of eccentric exercise when applied alone and combined with extrocoporeal shockwave therapy had been reported; however, the underlying treatment mechanisms of pain and dysfunction are not clear. This project aimed to explore the mechanical, physiological and therapeutic effects of eccentric exercise when applied as a single treatment and as an adjunct to extracorporeal shockwave therapy.


Recruitment information / eligibility

Status Completed
Enrollment 43
Est. completion date January 1, 2014
Est. primary completion date January 1, 2014
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Competitive athletes - Pain at the inferior pole of the patella with training for at least 3 months - Tenderness at the inferior pole of the patella on palpation Exclusion Criteria: - Patellofemoral pain syndrome, fat pad irritations, meniscus injury, osteoarthritis, rheumatoid arthritis or infections - History of fracture over lower limbs and inflammatory myopathies - Cortisone injuection and other interventions within 3 months - Contraindication to extracorporeal shockwave therapy

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Eccentric exercise
Knee eccentric exercise with sham or focused extrocorporeal shockwave therapy for 12 weeks

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
The Hong Kong Polytechnic University

Outcome

Type Measure Description Time frame Safety issue
Primary Tendon stress in pascals at baseline Tendon stress measured by ultrasonography and dynamometry Before intervention
Primary Change of tendon stress in pascals at 12 weeks Tendon stress measured by ultrasonography and dynamometry 12 weeks
Primary Change of tendon stress in pascals at 16 weeks Tendon stress measured by ultrasonography and dynamometry 16 weeks
Primary Tendon vascularity index as percentage at baseline Tendon vascularity measured by power doppler ultrasonography Before intervention
Primary Change of tendon vascularity index as percentage at 12 weeks Tendon vascularity measured by power doppler ultrasonography 12 weeks
Primary Change of tendon vascularity index as percentage at 16 weeks Tendon vascularity measured by power doppler ultrasonography 16 weeks
Secondary Tendon related pain on visual analogy scale at baseline Maximal intensity of self-perceived pain in the past 7 days, pain during single-leg declined-squat test Before intervention
Secondary Change of tendon related pain on visual analogy scale at 12 weeks Maximal intensity of self-perceived pain in the past 7 days, pain during single-leg declined-squat test 12 weeks
Secondary Change of tendon related pain on visual analogy scale at 16 weeks Maximal intensity of self-perceived pain in the past 7 days, pain during single-leg declined-squat test 16 weeks
Secondary Tendon related dysfunction by questionnaire at baseline Victorian Institute of Sport Assessment Questionnaire - Patellar Tendon Before intervention
Secondary Change of tendon related dysfunction by questionnaire at 12 weeks Victorian Institute of Sport Assessment Questionnaire - Patellar Tendon 12 weeks
Secondary Change of tendon related dysfunction by questionnaire at 16 weeks Victorian Institute of Sport Assessment Questionnaire - Patellar Tendon 16 weeks
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