Effect of Graston Technique on Planter Thickness in Patients With Planter Fasciitis
- Conditions
- Plantar Fascitis
- Interventions
- Other: Garston techniqueOther: exercise program
- Registration Number
- NCT06248853
- Lead Sponsor
- Cairo University
- Brief Summary
this study will be conducted to investigate the effect of Graston Technique on Planter Thickness in Patients With Planter Fasciitis
- Detailed Description
Plantar fasciitis (PF), generally a self-limiting condition, is identified as one of the most common causes of heel pain in adults. It affects both sedentary and athletic populations .
It may be considered that PF emerges due to excessive and prolonged standing or running, which causes an acute inflammation or micro-tears, and degenerative changes plantar fascia. The persistence of these risk factors inhibits the regular repair process thus collagen degeneration occurs, causing the structural changes of the plantar fascia. Numerous interventions have been described for treatment of PF, which include: Stretching calf or plantar region which is performed with the patient stands with staggered legs facing toward a wall, with both hands stretched out .The Graston technique can break up scar tissue and restore soft tissue. The Graston technique is a type of manual therapy in which patented stainless-steel instruments are used to restore soft tissue motion by breaking up scar tissue. fifty patients with planter fasciitis will be assigned randomly to two equal groups; first one will receive graston technique in addition to exercise program, the second one will receive exercise program only for six weeks
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 50
- patients that Clinically diagnosed cases of plantar fasciitis not less than 6 weeks.
- patients willing to precipitate in the study and take treatment for 6 successive weeks.
- Heel pain felt maximally over the plantar aspect of heel
- Pain in the heel on the first step in the morning
- No history of rest pain in the heel
- Subjects with clinical disorders where therapeutic ultrasound is contraindicated such as infective conditions of foot, tumor, calcaneal fracture, metal implant around ankle.
- Subjects with a clinical disorder where myofascial release is contraindicated as dermatitis.
- Subjects with impaired circulation to lower extremities
- Subjects with referred pain due to sciatica and other neurological disorders.
- Arthritis
- Corticosteroids injection in heel preceding 3 months
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Garston technique exercise program the patients will receive graston technique with exercise program three times aweek for six weeks Garston technique Garston technique the patients will receive graston technique with exercise program three times aweek for six weeks exercise program exercise program the patients will receive an exercise program three times a week for six weeks
- Primary Outcome Measures
Name Time Method plantar thickness up to six weeks Ultrasonography will be used to measure planter thickness
- Secondary Outcome Measures
Name Time Method pain pressure threshold up to six weeks The pressure algometer device will be used to measure pain pressure threshold
pain intensity up to six weeks Visual Analogue Scale (VAS) will be used to assess pain intensity: The VAS is a 100-mm horizontal line that may be used to quantify symptoms in a continuous fashion. Patients will instructed to indicate the intensity of their pain by marking on a line anchored by "no pain" on the left and "worst imaginable pain" on the right .
pain intensity at the first step up to six weeks numerical pain rating scale (NPRS) will be used to measure pain intensity at the first step. NPRS is a 10cm horizontal line t. Patients will instructed to indicate the intensity of their pain by marking on a line anchored by "no pain" on the left and "worst imaginable pain" on the right side.
functional levels of foot up to six weeks The Foot and Ankle Ability Measure (FAAM) questionnaire will be used to assess foot function. The FAAM is a self-reported questionnaire that comprehensively assesses the physical function of those with musculoskeletal conditions of the leg, foot, and ankle. It has a 21-item subscale for measuring the function of the individual with his or her activities of daily living (ADLs) and a ten-item subscale for measuring function with sports. The ADL subscale will be used for this study. The instrument is scored on a Likert scale from 4 to 0, with 4 representing ''no difficulty'' as going up stairs and 0 representing ''unable to do.'' The answers are then converted to a scale from 0 to 100, with a higher score representing a higher functional level.