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Clinical Trials/ISRCTN47272667
ISRCTN47272667
Completed
N/A

A randomized controlled trial to evaluate the effectiveness of insoles to treat plantar heel pain

SSL International (UK)0 sites150 target enrollmentJuly 31, 2008
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Overview

Phase
N/A
Intervention
Not specified
Conditions
Not specified
Sponsor
SSL International (UK)
Enrollment
150
Status
Completed
Last Updated
9 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
July 31, 2008
End Date
TBD
Last Updated
9 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
SSL International (UK)

Eligibility Criteria

Inclusion Criteria

  • •1\. Male or female participants between the ages of 18 and 65 years old
  • •2\. Participants with self\-reported plantar heel pain with a minimum of 4 weeks duration
  • •3\. Self\-reported plantar heel pain who score at least 40 mm on a 100 mm visual analogue scale (VAS) for pain
  • •4\. Participants with plantar heel pain in the 2 days prior to recruitment
  • •5\. Participants who agree to wear the insoles provided for at least 4 hours each day
  • •6\. Participants who give written informed consent

Exclusion Criteria

  • •1\. Participants reporting acute injury to the foot at the onset of the plantar heel pain
  • •2\. Participants with posterior or medial/lateral heel pain or any secondary pain elsewhere in the foot since the onset of plantar heel pain
  • •3\. Participants with significant musculo\-skeletal disease diagnosed such as rheumatoid arthritis, hip, knee or back pain
  • •4\. Participants with sensory or motor function disease such as diabetes
  • •5\. Participants who are pregnant or breast\-feeding
  • •6\. Participants who have received or self\-administered treatment for the heel pain in the previous 4 weeks
  • •7\. Participants who have received corticosteroid injection therapy in the heel in the previous 3 months
  • •8\. Participants that were previously in this study
  • •9\. Participants that were in another study within the last 3 months

Outcomes

Primary Outcomes

Not specified

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