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IRCT2017080525732N22 IRCT 2017-08-23 Deputy of Research and Technology, Semnan University of Medical Sciences The effect of dry needling on pain and Range of Motion of ankle joint and thickness of plantar fascia in patient with plantar fasciitis The effect of dry needling on pain and Range of Motion of ankle joint and thickness of plantar fascia in patient with plantar fasciitis 2017-08-23 anticipated 30 Complete https://irct.ir/trial/21498 interventional Randomization: N/A, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Prevention. 2 Plantar fasciitis. Intervention 1: Control group: In the control group will not perform any treatments and it just to compare with intervention group for level of thickness plantar fascia, the level of pain and range of motion will be measured at the beginning of the study and one month later. Intervention 2: Intervention group: Patients were undergoing to dry needle (according protocol). After dry needling for four weeks so once a week, examinations of the level of pain and range of motion and thickness plantar fascia will be performed. Also, one month after treatment, the variables will be measured again to follow up the treatment.
public Ziaeddin Safavi-Farokhi
Semnan University of Medical Sciences, Basij Blvd, Semnan
Semnan Iran (Islamic Republic of) 3514799442 +98 23 3345 1336 are20935@gmail.com Semnan University of Medical Sciences scientific Ziaeddin Safavi-Farokhi
Semnan University of Medical Sciences, Basij Blvd, Semnan
Semnan Iran (Islamic Republic of) 3514799442 +98 23 3345 1336 are20935@gmail.com Semnan University of Medical Sciences Iran (Islamic Republic of) Inclusion criteria: Patients with PFs in aged 40 to 60 years; having trigger point in gastro or soleus muscles or both of them; thickness plantar fascia more than 4 mm; foot pain in first steps in the morning and at least six months has passed since the onset of pain; the pain level in visual analog scale is at least four; non-athlete persons; plantar flexion or dorsi flexion is less than normal range. Exclusion criteria: Diabetes; hypersensitivity to needle; fear of needle; pregnancy; infection; peripheral neuropathy; hemophilia or coagulation problems; history of plantar fascia surgery; history of injection in the last three months. 40 years 60 years Both M72.2 Plantar fasciitis Rehabilitation Rehabilitation Control group: In the control group will not perform any treatments and it just to compare with intervention group for level of thickness plantar fascia, the level of pain and range of motion will be measured at the beginning of the study and one month later. Intervention group: Patients were undergoing to dry needle (according protocol). After dry needling for four weeks so once a week, examinations of the level of pain and range of motion and thickness plantar fascia will be performed. Also, one month after treatment, the variables will be measured again to follow up the treatment. Plantar Fascia Thickness. Timepoint: Before and after using a dry needle. Method of measurement: Ultrasonography. Deputy of Research and Technology, Semnan University of Medical Sciences Approved 2017-07-24 Ethics committee of Semnan University of Medical Sciences Semnan University of Medical Sciences, Basij Blvd, Semnan semnan Iran (Islamic Republic of)