Plantar heel pain. A pragmatic randomized single blinded clinical trial comparing the use of customized insoles, night splints and a barefoot technology shoe.
Recruiting
- Conditions
- heel pain syndrome heelspur10013361
- Registration Number
- NL-OMON34189
- Lead Sponsor
- Slotervaartziekenhuis
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 70
Inclusion Criteria
Patients 18 years old or older
Pain and tenderness under the heel on weight bearing with associated limitation of activity.
Pain should be present for a minimum of 6 weeks.
Patients must be willing and able to sign the informed consent
Exclusion Criteria
Achilles tendon injury
Acute traumatic rupture of the plantar fascia
Patients with a rigid hindfoot valgus or varus
Patients with ankle or foot arthritis
Patients with chronic ankle instability
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Pain Visual Analog Scale<br /><br>Foot Function Index-5pt (Verbal Rating Scales). </p><br>
- Secondary Outcome Measures
Name Time Method <p>Satisfaction VAS</p><br>