Status:

COMPLETED

Manual Therapy and Exercise Versus Home Exercises in the Management of Patients Status Post Ankle Sprain

Lead Sponsor:

Franklin Pierce University

Conditions:

Ankle Sprain

Eligibility:

All Genders

16-60 years

Phase:

NA

Brief Summary

A recent study has demonstrated that a physical therapist directed exercise program did not result in greater reductions in disability and pain when compared to a home exercise program. However, no ma...

Eligibility Criteria

Inclusion

  • Inclusion/Exclusion Criteria:
  • A combination of physical examination and self-report measures will be used to assess the patient's potential eligibility according to each inclusion/exclusion criterion.
  • The following inclusion criteria will be used to determine eligibility for this study:
  • Primary complaint of ankle pain, status post inversion ankle sprain.
  • The investigators decided to include patients with both acute and chronic ankle sprains since our previous work has shown that patients from both stage have exhibited positive benefits with manual therapy.66
  • Age between 16-60 years old
  • NPRS score \> 3 points (average score) over past 24 hrs.
  • Does not meet criteria for needing radiographs per the Ottawa Ankle Rules
  • The following exclusion criteria will be used to determine ineligibility for this study:
  • Red flags noted in the patient's Medical Screening Questionnaire (i.e. tumor, fracture, RA, osteoporosis, prolonged history of steroid use, severe vascular disease, etc.)
  • Prior surgery to the distal tibia, fibula, ankle joint, or rearfoot region (proximal to the base of the metatarsals).
  • Grade III ankle sprain (as defined by the West Point Ankle Sprain Grading System and/or tenderness along the anterior medial malleolus as described by,51 fracture, or other absolute contraindications to manual therapy.
  • Insufficient English language skills to complete all questionnaires
  • Inability to comply with treatment and follow-up schedule

Exclusion

    Key Trial Info

    Start Date :

    November 1 2008

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ACTUAL

    End Date :

    June 1 2012

    Estimated Enrollment :

    74 Patients enrolled

    Trial Details

    Trial ID

    NCT00797368

    Start Date

    November 1 2008

    End Date

    June 1 2012

    Last Update

    July 9 2013

    Active Locations (3)

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    Page 1 of 1 (3 locations)

    1

    Colorado University

    Denver, Colorado, United States, 80221

    2

    Regis University

    Denver, Colorado, United States, 80221

    3

    Concord Hospital

    Concord, New Hampshire, United States, 03301