The goal of this randomized controlled clinical trial is to evaluate whether Fascial Manipulation (FM) or Dry Needling (DN) can effectively reduce pain, improve functional mobility, and enhance range of motion (ROM) in individuals with chronic Plantar Fasciitis (PF) aged 25-45 years The main questions it aims to answer are: * Does Fascial Manipulation significantly reduce pain intensity in patients with chronic Plantar Fasciitis? * Does Dry Needling provide comparable or superior improvements in functional mobility and ankle-foot ROM compared to Fascial Manipulation? Researchers will compare the Fascial Manipulation group to the Dry Needling group to determine which intervention is more effective in improving pain and functional outcomes in chronic PF. Participants will: Receive either Fascial Manipulation or Dry Needling interventions according to their assigned group. Attend treatment sessions twice a week for six weeks. Undergo baseline, mid, and post-intervention assessments of pain (VAS-100scale), functional mobility (FFI), diagnostic (PFPS, Windlass, and ankle-foot range of motion (goniometric measurements).
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Foot Function Index (FFI):
Timeframe: 3 weeks
Visual Analog Scale (VAS 100):
Timeframe: 3 weeks
Plantar Fasciitis Pain/Disability Scale (PFPS)
Timeframe: 3 weeks
Goniometry
Timeframe: 3 weeks