The main goal of this study is to determine if a specific acupuncture technique-targeting a "heel pain point" located on the hand-is an effective and safe way to treat heel pain. Specifically, the researchers want to: Measure Pain Relief: Evaluate how effectively the treatment reduces pain levels. Check Physical Function: Determine if the treatment helps patients walk and move more comfortably. Ensure Safety: Track any side effects or adverse reactions to confirm the treatment is safe for patients. Target Population The study is looking for participants who meet the following criteria: Age: Adults between 40 and 70 years old. Diagnosis: Individuals diagnosed with heel pain (plantar fasciitis). Duration: People who have had the pain for less than two months and have not recently received other related treatments. Typical Symptoms: Individuals who experience significant pain during their first few steps in the morning or after sitting for a long time. Exclusions: The study excludes people with recent foot injuries, gout, or serious underlying health conditions such as severe diabetes or heart disease. Primary Research Endpoint The "Primary Endpoint" is the specific result the researchers use to decide if the treatment was successful: The 50% Reduction Goal: The study measures the "response rate," which is the percentage of patients whose pain score decreases by at least 50% compared to their starting pain level. Evaluation Timing: This success measure is evaluated after the patient completes one full course of treatment, which consists of 10 sessions given over approximately 20 days.
Age range
40 Years – 70 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
The response rate after one course of acupuncture intervention (defined as the proportion of subjects achieving a ≥50% reduction in VAS score from baseline)
Timeframe: 20 days