Actively Recruiting
Effect of Cognitive Training Combined with Stretching and Strengthening Exercises on Pain, Foot Function, and Balance in Patients With Plantar Fasciitis
Led by Beni-Suef University · Updated on 2026-05-06
80
Participants Needed
1
Research Sites
3 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Plantar fasciitis is a condition caused by degeneration of the plantar fascia due to repetitive stress, leading to heel pain and impaired balance during weight-bearing activities. This trial evaluates whether adding cognitive training exercises to stretching and strengthening exercises improves pain, foot function, and static balance better than stretching and strengthening exercises alone. The study is a randomized controlled trial designed to assess the effects of cognitive and neuromuscular control training on musculoskeletal function in people with plantar fasciitis. Participants will be randomly assigned to one of two groups. The cognitive training group will perform a structured program integrating attention-demanding dual-task exercises with functional movement tasks, alongside stretching and strengthening exercises targeting the plantar fascia and lower limb muscles. The control group will perform only the conventional stretching and strengthening exercises focusing on flexibility and muscle tightness reduction. Exercise sessions will be conducted progressively over the intervention period based on participant performance. During the study, assessments will be made at the start and after 4 weeks of treatment to measure pain intensity using a visual analog scale, foot functional disability, and static balance. Participants must be able to stand and complete basic balance and functional tests. Researchers will monitor outcomes to compare how cognitive training combined with physical exercises affects pain, function, and balance compared to physical exercises alone. The total participation period will last 4 weeks.
CONDITIONS
Brief Title
Cognitive Training for Pain , Balance and Foot Function in Plantar Fasciitis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 18 to 60 years
- Clinically diagnosed with plantar fasciitis by a physician or physiotherapist
- Experiencing heel pain for at least 4 weeks
- Ability to stand and perform basic functional and balance tests
- Willingness to participate and provide informed consent
- Not currently receiving other structured physical therapy or cognitive training programs during the study period
You will not qualify if you...
- History of lower limb surgery or fractures affecting the foot or ankle
- Presence of neurological disorders affecting balance or motor control (e.g., stroke, Parkinson's disease)
- Systemic inflammatory or rheumatologic conditions (e.g., rheumatoid arthritis)
- Severe musculoskeletal deformities of the lower limb or foot
- Recent corticosteroid injection in the heel region within the last 3 months
- Current participation in other structured rehabilitation or exercise programs
- Pregnancy (if applicable due to balance and biomechanical changes)
- Inability to understand or follow instructions related to the intervention
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 4 weeks
Participants receive either a structured cognitive training program combined with functional movement tasks or a conventional stretching and strengthening exercise program targeting the plantar fascia and related lower limb muscles. The interventions focus on improving pain, functional disability, and static balance through progressive exercises over the treatment period.
Multiple visits during the 4-week treatment period
Trial Site Locations
Total: 1 location
1
Outpatient clinics of the Faculty of Physical Therapy, Beni Suef University
Cairo, Egypt
Actively Recruiting
Research Team
S
Sahar M Abdelmutilibe, PHD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
Frequently Asked Questions
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