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Reliability of Functional Outcome Measures in Plantar Fascitis Patients

Reliability of Functional Outcome Measures in Plantar Fascitis Patients

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01145118
Enrollment
80
Registered
2010-06-16
Start date
2010-07-31
Completion date
2011-05-31
Last updated
2012-01-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Plantar Fasciitis

Keywords

Plantar Fasciitis, Physiotherapy

Brief summary

Plantar Fasciitis (PF) is the most common foot condition treated by healthcare providers, striking approximately 2 million Americans each year. Nevertheless its causes are still not known. The risk factors for PF are known and the diagnosis, which is based on clinical assessment, is relatively simple. Still most of the treatments for PF focus on short term symptoms relief instead of prevention or reduction of recurrence. Physical therapy treatment that focuses on reducing the symptoms for the long run and prevention, should include outcome measures, which if found to be reliable, will make the diagnosis clearer. Diagnosis based on reliable clinical and functional measures will assist the physical therapist to understand the major deficiencies of the patient, and accordingly to help him to make the right decision in choosing treatment. Also comprehensive knowledge of the characteristics of PF may enable selection of appropriate preventive measures.

Detailed description

Objectives: Characterize the unilateral PF syndrome using functional outcome measures, while comparing them to the healthy foot of the same patient. In addition the study will investigate the reliability of these functional outcome measures in PF patients. Methodology: Individuals referred to physiotherapy for PF will be assessed for eligibility and consent for the study. They will undergo two evaluations on the same week to evaluate the test- retest reliability of the functional measurements.

Interventions

None listed

Sponsors

Clalit Health Services
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
21 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Unilateral plantar fasciitis * Painful first step in the morning * Calcaneal soreness in palpation * Insured by Clalit Health Care Services * Signed informed consent

Exclusion criteria

* Ankle or foot surgery * Congenital deformation of foot * Lower limb spasticity * Using assistive devices * Bilateral plantar fasciitis * Refuse to participate or sign informed consent

Design outcomes

Primary

MeasureTime frameDescription
Functional Limitation1 weekMeasurement of Functional Limitation using Foot Function Index (FFI) compared to the healthy foot

Secondary

MeasureTime frameDescription
Pain intensity1 weekMeasurement of pain intensity using visual analog scale (VAS), compared to the healthy foot
Pain threshold1 weekMeasurement of pain threshold using a Pressure Algometer, compared to the healthy foot
Muscle strength1 weekMeasurement of Muscle strength in Plantar Flexion and Dorsi Flexion using Hand Held Dinamometer - compared to the healthy foot.
Range of motion1 weekMeasurement of Range of motion using a Digital inclinometer - compared to the healthy foot

Countries

Israel

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026