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A Clinical Study on the Efficacy of Electric-Heated Bian Stone Combined with Fascial Manipulation in the Treatment of Plantar Fasciitis

A Clinical Study on the Efficacy of Electric-Heated Bian Stone Combined with Fascial Manipulation in the Treatment of Plantar Fasciitis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026001578
Enrollment
Unknown
Registered
2026-06-23
Start date
2026-06-22
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Plantar fasciitis

Interventions

1: Electric-Heated Bian Stone Combined with Fascial Manipulation
2:Fascial Manipulation

Sponsors

Guizhou Hospital of Guangdong Provincial Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
21 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1) Age 21–70 years; 2) Meets the diagnostic criteria for plantar fasciitis as outlined in the clinical practice guidelines of the International Classification of Functioning, Disability and Health-Heel Pain/Plantar Fasciitis: 2014 Revision, primarily including pain on the medial aspect of the sole, heel pain triggered by a recent increase in weight-bearing activities, tenderness on palpation at the proximal attachment of the plantar fascia, and a positive Windlass test. 3) Duration of symptoms exceeding 3 months; 4) No oral or injectable use of steroids or nonsteroidal anti-inflammatory drugs (NSAIDs) within the past 3 months; 5) No history of lower limb surgery within the past year; 6) Agreement to participate in this study and signing of the informed consent form.

Exclusion criteria

Exclusion criteria: 1) Fractures of the ankle or strains of tendons and ligaments, or symptoms of nerve compression in the lower extremities; 2) Patients with lumbar disc herniation compressing the nerve roots; 3) Calcaneal osteomyelitis; 4) Patients with infections, tumors, severe osteoporosis, tuberculosis, or cardiac or renal insufficiency; 5) Patients with cognitive impairment or those who are unable to cooperate or unwilling to participate in the trial.

Design outcomes

Primary

MeasureTime frame
Visual Analogue Scale (VAS);Foot and Ankle Ability Measure (FAAM);

Secondary

MeasureTime frame
Numerical Rating Scale;Treatment duration (t);

Countries

China

Contacts

Public ContactDuan Chunxing

Guizhou Hospital of Guangdong Provincial Hospital of Traditional Chinese Medicine

duancx10@126.com+86 18565436609

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Aug 10, 2026