Not Yet RecruitingNot Applicable

INIT Versus IASTM In Patients With Chronic PF

54 participantsStarted 2024-07-01

Plain-language summary

1. To investigate integrated neuromuscular inhibition versus Instrument assisted soft tissue mobilization on general pain intensity in patient with chronic plantar fasciitis. 2. To investigate integrated neuromuscular inhibition versus Instrument assisted soft tissue mobilization on pain intensity at initial morning step in patient with chronic plantar fasciitis. 3. To investigate integrated neuromuscular inhibition versus Instrument assisted soft tissue mobilization on pain pressure threshold in patient with chronic plantar fasciitis. 4. To investigate integrated neuromuscular inhibition versus Instrument assisted soft tissue mobilization on active dorsiflexion ROM in patient with chronic plantar fasciitis. 5. To investigate integrated neuromuscular inhibition versus Instrument assisted soft tissue mobilization on functional disability in patient chronic plantar fasciitis. 5\) Investigate integrated neuromuscular inhibition versus Instrument assisted soft tissue mobilization on functional disability in patient chronic plantar fasciitis.

Who can participate

Age range40 Years – 60 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Patient with history of plantar fasciitis more than three months ago. * Plantar heel pain with first few steps upon walking in the morning and after prolonged rest. * Patient\'s Age between 40-60 years old. * Patient\'s Body mass index (BMI 18 to 29.9kg/m2). Exclusion Criteria: * Patients with any prior surgery to distal tibia, fibula, ankle joint or rear foot region. * Presence of any red flags i.e., tumor, fracture, and heterotrophic ossification and had acute inflammatory condition at ankle-foot region were excluded from the study. * Deformity of foot and ankle complex and subjects with referred pain due to sciatica and other neurological disorder.

What they're measuring

general pain intensity

Timeframe: change of general pain intensity through 4 weeks

Trial details

NCT IDNCT06493487

SponsorCairo University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-08-01

Contact for this trial

esraa khairy afify esmail, B.Sc

+2(02)01013982552 ekhairy851@gmail.com