Plantar fasciitis. Plantar fascial fibromatosis
Conditions
Interventions
Intervention 1: Intervention group: designed orthosis based on dynamic plantar pressure distribution + Night splint + Diclofenac 25mlgr, 3times per day (75 mlgr). Intervention 2: Control group: Night
Treatment - Devices
Intervention group: designed orthosis based on dynamic plantar pressure distribution + Night splint + Diclofenac 25mlgr, 3times per day (75 mlgr)
Control group: Night splint + Diclofenac 25mlgr, 3times per days (75 mlgr)
Sponsors
Vice-Chancellor for Research-University of Social Welfare and Rehabilitation Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: early symptoms of chronic plantar fasciitis; age from 18 to 60 years old; no history of leg surgery; no systemic inflammatory diseases ( such as rheumatoid arthritis, ankylosing spondylitis, Reiter 's syndrome and diabetes); no foot fracture; no lower back pain with radicular pain; no deformity heels; no use nonsteroidal anti-inflammatory drugs in the last six months of physiotherapy to treat inflammation of the sheath foot plantar and untreated; no use of nonsteroidal anti-inflammatory drugs during the past six weeks, even for pain and inflammation in other parts of the body. Exclusion criteria: failure to follow the treatment program during the study; inaccuracy in the implementation of the proposed treatment; use other treatments along with treatment designated in the study; it is diagnosed by the criteria above specialist.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Plantar fascia thickness. Timepoint: Before entering the study - one month after intervention. Method of measurement: Ultrasonography application.;Pain. Timepoint: Before entering the study - one month after intervention. Method of measurement: Foot and Ankle Outcome Score (FAOS)-Pain Subscale.;Quality of Life. Timepoint: Before entering the study - one month after intervention. Method of measurement: Foot and Ankle Outcome Score (FAOS)- Quality of Life Subscale.;Function, Daily living. Timepoint: Before entering the study - one month after intervention. Method of measurement: Foot and Ankle Outcome Score (FAOS)-Function, daily living Subscale.;Maximum plantar pressure. Timepoint: Before entering the study - one month after intervention. Method of measurement: Emed Platform.;Maximum force. Timepoint: Before entering the study - one month after intervention. Method of measurement: Emed Platform.;Pressure-time integrals. Timepoint: Before entering the study - one month after intervention. Method of measurement: Emed Platform.;Force-time integral. Timepoint: Before entering the study - one month after intervention. Method of measurement: Emed Platform.;Contact area. Timepoint: Before entering the study - one month after intervention. Method of measurement: Emed Platform.;Arch Index. Timepoint: Before entering the study - one month after intervention. Method of measurement: Emed Platform. | — |
Secondary
| Measure | Time frame |
|---|---|
| Height. Timepoint: Before entering the study. Method of measurement: Stadiometer.;Weight. Timepoint: Before entering the study. Method of measurement: Bathroom scales.;Body Mass Index. Timepoint: Before entering the study. Method of measurement: BMI Formula.;Standing Duration. Timepoint: Before entering the study. Method of measurement: Patient Self-report.;Direction of pain. Timepoint: Before entering the study. Method of measurement: Physical examination. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMasoomeh Nakhaee
Department of Orthotics and Prosthetics, University of Social Welfare and Rehabilitation Sciences
Outcome results
None listed