Study of Quantification of Hyperpronation

NCT ID: NCT01587612

Last Updated: 2014-03-31

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

80 participants

Study Classification

OBSERVATIONAL

Study Start Date

2003-08-31

Study Completion Date

2004-03-31

Brief Summary

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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.

Detailed Description

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Conditions

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Foot Pain Chronic

Keywords

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Pain Foot

Eligibility Criteria

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Inclusion Criteria

* Hyperpronation of foot
* Consent of information

Exclusion Criteria

* Normal gait
* Lack of consent of information
* Unable to speak and read Danish
Minimum Eligible Age

18 Years

Maximum Eligible Age

68 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Northern Orthopaedic Division, Denmark

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Mogens B Laursen, MD

Role: PRINCIPAL_INVESTIGATOR

Northern Orthopaedic Division

Locations

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Northern Orthopaedic Division, Klinik Aalborg

Aalborg, Northern Jutland, Denmark

Site Status

Countries

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Denmark

Other Identifiers

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ON-02-005-OSi

Identifier Type: -

Identifier Source: org_study_id