Heel pain showdown: which therapy wins for plantar fasciitis?
NCT ID NCT07426783
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested two treatments—fascial manipulation and dry needling—in 36 women aged 25-45 with chronic plantar fasciitis (long-term heel pain). Participants received one of the treatments twice a week for six weeks. The goal was to see which method better reduces pain and improves foot function and movement.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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36 people
The number who actually took part.
- Started
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Oct 2025
- Finished
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Mar 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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25 to 45 years
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: Participants falling in this category would be recruited into the study. * Females aged 25-45 years with chronic heel pain with symptoms persisting for more than one month. * Having a heel pain on the first step during the last week with the rate of at least 40 mm on visual analogue scale. * Presence of morning heel pain, tenderness at the medial calcaneal tubercle, and heel spur, or pain exacerbated by prolonged standing, walking, or dorsiflexion * Patients accepting to discontinue analgesics, non-steroidal anti-inflammatory medications and oral/topical paracetamol during the study period. * Patients diagnosed with plantar fasciitis using Plantar fasciitis questionnaire. Exclusion Criteria: Participants fall in this category would be excluded of the study. * History of foot or ankle fractures, surgeries, or inflammatory conditions like RA. * Presence of any neurological disorders affecting gait. * Participants with diagnosed tendinopathies, including Achilles tendinopathy, posterior tibial tendinopathy, etc. will be excluded from the study to ensure the specificity of plantar fasciitis. * Participants with metabolic disorders (e.g., osteomalacia, osteoporosis, rheumatoid arthritis, diabetes) affecting bone and soft tissue integrity will be excluded to prevent confounding effects on pain, healing, and treatment outcomes * Active infections, open wounds, or skin conditions at the treatment site. * Diabetic neuropathy or vascular insufficiencies that may affect healing and sensations. * Patients with bleeding disorders like hemophilia and those on anti-coagulant therapy. * Patients with hypersensitivity reactions to needles or specific metals used in needles. * Patients with needle phobia. * Patients with history of epilepsy or seizures. * Use of corticosteroid injections, shockwave therapy, or other invasive treatments for PF in the last 3 months. * Participation in another clinical trial or conflicting therapy during the study period
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Railway General Hospital
Rawalpindi, Punjab Province, Pakistan
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Other studies related to the condition(s) this trial covers.
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