Study of Quantification of Hyperpronation

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT01587612
Recruitment Status : Completed
First Posted : April 30, 2012
Last Update Posted : March 31, 2014
Information provided by (Responsible Party):
Northern Orthopaedic Division, Denmark

Brief Summary:

Hyperpronation is af frequent cause of excessive load in foot and crus. Pain and limited functional ability cause problems with work-related activities, sport activities and leisure activities.

There are only few studies of the frequency of pain related to hyperpronation in foot and the effect of exercises. Medics and physiotherapists need sufficient evidence-based knowledge to treat these patients correctly.

Therefore, the investigators want to study the effect of exercises and inner soles for treatment of patients with chronic pain and hyperpronation of foot.

Condition or disease
Foot Pain Chronic

Study Type : Observational
Actual Enrollment : 80 participants
Official Title: Study of Quantification of Hyperpronation
Study Start Date : August 2003
Actual Primary Completion Date : December 2003
Actual Study Completion Date : March 2004

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Foot Health
U.S. FDA Resources

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 68 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Hyperpronation of foot

Inclusion Criteria:

  • Hyperpronation of foot
  • Consent of information

Exclusion Criteria:

  • Normal gait
  • Lack of consent of information
  • Unable to speak and read Danish

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT01587612

Northern Orthopaedic Division, Klinik Aalborg
Aalborg, Northern Jutland, Denmark
Sponsors and Collaborators
Northern Orthopaedic Division, Denmark
Principal Investigator: Mogens B Laursen, MD Northern Orthopaedic Division

Responsible Party: Northern Orthopaedic Division, Denmark Identifier: NCT01587612     History of Changes
Other Study ID Numbers: ON-02-005-OSi
First Posted: April 30, 2012    Key Record Dates
Last Update Posted: March 31, 2014
Last Verified: March 2014

Keywords provided by Northern Orthopaedic Division, Denmark: