To assess whether the provision of a tension night splint (TNS) device has any additional benefit in patients with chronic plantar fasciitis, compared to routine care comprising physiotherapy \& podiatry alone.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
40
this is the use of a commercially available tension night splint device, to be worn by the patient
this is the standardised structured rehabilitation programme of home exercises given to patients, with supporting literature, and instructions on how to progress the regime themselves
University Hospitals of Leicester NHS Trust
Leicester, United Kingdom
Reduction in pain as assessed by a 0-10 visual analogue scale (VAS)
Time frame: primary outcome time = 3 months
improvement in function as assessed by validated PROMs as described below
several validated Patient rated Outcome Measures (PROMS) are used in this study, including: FFI-r, FAAM, and MOXFQ
Time frame: 3 months - end point
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