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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00952042
Other study ID # Kongsgaard2
Secondary ID
Status Completed
Phase N/A
First received August 3, 2009
Last updated July 18, 2014
Start date July 2009
Est. completion date October 2012

Study information

Verified date July 2014
Source University of Copenhagen
Contact n/a
Is FDA regulated No
Health authority Denmark: The Regional Committee on Biomedical Research Ethics
Study type Interventional

Clinical Trial Summary

The use of eccentric resistance training as management of Achilles tendinopathy is widespread. The investigators have recently demonstrated that heavy slow resistance training was superior in the management of patellar tendinopathy.

Hypothesis: heavy slow resistance training is more effective than eccentric resistance training in the clinical management of Achilles tendinopathy.


Recruitment information / eligibility

Status Completed
Enrollment 47
Est. completion date October 2012
Est. primary completion date October 2012
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- Unilateral Achilles tendon pain,

- Symptoms for at least three months,

- Ultrasonographical tendon abnormalities, AND

- Able to comply with both intervention arms.

Exclusion Criteria:

- Bilateral symptoms,

- Previous surgery below knee,

- Corticosteroid injections below the knee during past year,

- Hypercholesterol,

- Diabetes, OR

- Arthritis.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Other:
Heavy slow resistance training
Heel-raises. 12-6RM. each contraction performed slowly. three times weekly for 12 weeks
Eccentric resistance training
Eccentric heel-raises. 3 x 15 reps performed twice daily for 12 wks.

Locations

Country Name City State
Denmark Institute of Sports Medicine Copenhagen. Bispebjerg Hospital Copenhagen NV

Sponsors (1)

Lead Sponsor Collaborator
University of Copenhagen

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary VISA-A score 0,12 wks + 1yr follow-up No
Secondary Tendon thickness 0,12 wks + 1yr follow-up No
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