Actively Recruiting

Phase Not Applicable
Age: 18Years - 70Years
All Genders
ID07628218

Clinical Effectiveness of Video-Based Exercise Training Compared With Physician-Led Face-to-Face Exercise Instruction in Patients With Plantar Fasciitis: A Randomized Non-Inferiority Trial

Led by Balikesir Ataturk City Hospital · Updated on 2026-06-04

300

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating two different methods of exercise instruction for adults with plantar fasciitis, a common cause of chronic heel pain that can limit function and reduce quality of life. The study compares face-to-face exercise guidance by an orthopedic physician with video-based exercise instruction delivered via a QR code or web link. Both methods provide the same exercise content, aiming to determine if the video-based approach is not worse than the physician-led method in improving foot function. Participants will be randomly assigned to one of two groups. One group receives in-person training, where the physician demonstrates exercises including plantar fascia stretching, calf stretching, self-massage, toe raises, and towel pull exercises. The other group receives access to a standardized exercise video to perform the same exercises at home. All participants also receive standard education on plantar fasciitis management, including footwear advice, weight control, pain relief options, and support devices. Participants will be assessed at the start, 1 month, and 3 months after starting the exercise program. Researchers will measure changes in foot function using the Foot Function Index and pain levels with a numeric rating scale. They will also track exercise knowledge, adherence, education time, video viewing habits, any additional treatments needed, and patient satisfaction. The primary outcome is the change in foot function score from baseline to 3 months.

CONDITIONS

Brief Title

Video-Based Versus Physician-Led Exercise Training for Plantar Fasciitis

Who Can Participate

Age: 18Years - 70Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 to 70 years
  • Clinical diagnosis of plantar fasciitis
  • Plantar heel pain lasting for at least 3 months
  • Heel pain most prominent with first steps in the morning or after rest
  • Tenderness on palpation of the medial calcaneal tubercle
  • Baseline heel pain score of 4 or higher on a 0-10 scale
  • Functional capacity to perform prescribed exercises
  • Access to a smartphone, tablet, or computer to view exercise video
  • Ability to provide written informed consent
Not Eligible

You will not qualify if you...

  • Previous foot or ankle surgery on the affected side
  • History of foot fracture, tumor, advanced neuropathy, Charcot arthropathy, or tarsal tunnel syndrome
  • Interventional treatments for plantar fasciitis within the last 6 months (e.g., corticosteroid injection, shock wave therapy, platelet-rich plasma)
  • Inflammatory arthritis or systemic rheumatologic disease affecting the foot
  • Severe knee or hip osteoarthritis limiting exercise
  • Severe cognitive impairment preventing participation or questionnaire completion
  • Pregnancy
  • Inability or unwillingness to comply with the study protocol

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 3 months

Participants receive standardized education about plantar fasciitis and perform a home exercise program either through physician-led face-to-face instruction or via video-based exercise instruction.

1 baseline visit and 2 follow-up visits at 1 and 3 months

Trial Site Locations

Total: 1 location

1

Balikesir Ataturk City Hospital

Balıkesir, Turkey (Türkiye), +90(543)673-3113

Actively Recruiting

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Research Team

G

gunes SARIKAYA

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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