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Effect of Graston Technique on Planter Thickness in Patients With Planter Fasciitis

Not Applicable
Not yet recruiting
Conditions
Plantar Fascitis
Interventions
Other: Garston technique
Other: 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
Inclusion Criteria
  • 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
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Exclusion Criteria
  • 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
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Garston techniqueexercise programthe patients will receive graston technique with exercise program three times aweek for six weeks
Garston techniqueGarston techniquethe patients will receive graston technique with exercise program three times aweek for six weeks
exercise programexercise programthe patients will receive an exercise program three times a week for six weeks
Primary Outcome Measures
NameTimeMethod
plantar thicknessup to six weeks

Ultrasonography will be used to measure planter thickness

Secondary Outcome Measures
NameTimeMethod
pain pressure thresholdup to six weeks

The pressure algometer device will be used to measure pain pressure threshold

pain intensityup 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 stepup 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 footup 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.

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