Specific Acupuncture Protocol for the Treatment of Plantar Fasciosis

Not Applicable

Completed

• Conditions: Plantar Fascitis
• Interventions: Device: Intervention + Standard of care; Other: Standard of care

• Registration Number: NCT04243343
• Lead Sponsor: brett rasmussen

Brief Summary

Determine if the addition of a specific acupuncture protocol to a standard of care prescribed exercise program is more effective at improving pain and function in adult patients with plantar fasciosis.

Detailed Description

This is a randomized, controlled, multi-site trial investigating whether a specific acupuncture protocol can improve pain and function in adults with plantar fasciosis when added to standard of care treatment. The investigators hypothesize that there will be a significant improvement in both pain and functional outcomes, both acutely and over time, in the experimental group compared to the control group.

Study Timeline

• Study First Submitted: 2020-01-22
• Study First Submitted QC: 2020-01-24
• Study First Posted: 2020-01-28
• Study Start: 2020-06-01
• Primary Completion: 2021-11-02
• Study Completion: 2021-11-02
• Status Verified: 2022-01
• Last Update Submitted: 2022-01-13
• Last Update Posted: 2022-01-28

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 72

Inclusion Criteria

• Male and female DoD beneficiaries, aged 18 to 74 years, who have been diagnosed with plantar fasciosis (in one or both of their feet) OR
• Patients meeting criteria of pain in the bottom of the foot/heel with first steps in the morning & tender to palpation over the medial calcaneal tubercle (where the plantar fascia inserts).

Those with acute and chronic diagnoses will be included.

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Exclusion Criteria

• Pregnant

• Any of the following in the foot being included into the study:

  • Active cellulitis of lower extremity
  • Prior surgery for plantar fasciosis
  • Steroid injections in the last 12 weeks for plantar fasciosis; if received in last 12 weeks subjects will be offered to be involved in the study after they have completed a 12 -week wash out period.
  • If they have every had any prior acupuncture for plantar fasciosis using the defined Deep Ankle Local Periosteal points, any regenerative therapy to include proliferation therapy or platelet rich plasma therapy in the last 12 weeks for plantar fasciosis; if received in last 12 weeks subject will be offered to be involved in the study after they have completed a 12-week wash out period.
  • Botox injections for plantar fasciosis injections in the last 12 weeks for plantar fasciosis; if received in last 12 weeks subject will be offered to be involved in the study after they have completed.

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Intervention + Standard of care	Intervention + Standard of care	Acupuncture with electrostimulation plus standard of care prescribed home exercise program.
Standard of care	Standard of care	Standard of care prescribed home exercise program.

Primary Outcome Measures

Name	Time	Method
Foot function index revised short (FFI-R short)	visit 5 (week 12)	FFI-R short uses a likert questionnaire to document foot pain severity, foot stiffness, difficulty performing activities, activity limitation, and social issues related to affected foot.; It consists of 23 self-reported items divided into 3 subcategories on the basis of patient values: pain, disability and activity limitation.The patient has to score each question on a scale from 0 (no pain or difficulty) to 10 (worst pain imaginable or so difficult it requires help), that best describes their foot over the past week.
Defense and Veterans Pain Rating Scale Supplemental Questions	The DVPRS consists of an 11-point numerical rating scale with 0 indicating no pain and 10 indicating severe pain. visit 5 (week 12)	For clinicians to evaluate the biopsychosocial impact of pain.
Defense and Veterans Pain Rating Scale (DVPRS)	visit 5 (week 12)	The DVPRS consists of an 11-point numerical rating scale with 0 indicating no pain and 10 indicating severe pain. It has been confirmed for reliability and validity in measuring both acute and chronic pain, and is currently the standard for pain measurement throughout DoD and VA health systems. The DVPRS has demonstrated linear scale qualities allowing parametric methods to be used

Trial Locations

Locations (3)

Scott AFB; 🇺🇸 Belleville, Illinois, United States

Mike O'Callaghan Military Medical Center; 🇺🇸 Nellis Air Force Base, Nevada, United States

96th Medical Group; 🇺🇸 Eglin Air Force Base, Florida, United States