Participants who were diagnosed with chronic plantar fasciitis Plantar fasciitis
Conditions
Interventions
The intervention involved participants using the Plantar fasciitis device for pain relief. Each participant utilized the device for 12 sessions, spread over one month with a frequency of three times p
Experimental Device
Using Plantar Fasciitis Device
Sponsors
National Science Research and Innovation Fund (NSRF)
Eligibility
Sex/Gender
All
Age
18 Years to 85 Years
Inclusion criteria
Inclusion criteria: 1. Males and females aged 18-85 years with a medical diagnosis of chronic plantar fasciitis in one foot. 2. Body Mass Index (BMI) not exceeding 29.9
Exclusion criteria
Exclusion criteria: 1. Participants with a history of surgery on the ankle of the affected foot with chronic plantar fasciitis. 2. Participants with open wounds on the sole of the affected foot with chronic plantar fasciitis. 3. Participants with other neurological issues, such as stroke (ischemic, hemorrhagic, or occlusive) or movement disorders (e.g., Parkinson's disease). 4. Participants with unsuitable for testing by a physical therapist due to fatigue, fever, or general discomfort.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain Pre- and post-intervention in each session Dolorimeter, Numeric rating scale (NRS) | — |
Secondary
| Measure | Time frame |
|---|---|
| Range of motion (Ankle and Metatarsophalangeal joints ) Pre- and post-intervention in each session Goniometer,Foot ability Pre- and post-intervention Foot and Ankle Ability Measure: FAAM,Foot pain Pre- and post-intervention (Plantar Fasciitis Pain/Disability Scale: PFPS | — |
Countries
Thailand
Contacts
Public ContactKittichai Tharawadeepimuk
College of Sports Science and Technology, MAHIDOL UNIVERSITY
Outcome results
None listed