Skip to main content
Clinical Trials/NCT07571122
NCT07571122RecruitingNot Applicable

Effect of Cognitive Training on Pain , Foot Function, and Balance in Patients With Planter Fasciitis : A Randomized Controlled Trial

Beni-Suef University1 site in 1 country80 target enrollmentStarted: February 3, 2026Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
80
Locations
1
Primary Endpoint
Pain by VAS

Study Overview

Brief Summary

This randomized controlled trial aims to compare the effects of cognitive training exercises versus stretching and strengthening exercises on pain, functional dilatability, and static balance. Participants will be assigned to two groups: a cognitive training group or a stretching and strengthening exercise group. The cognitive training group will perform exercises targeting cognitive and neuromuscular control plus stretching and strengthening exercise , while the control group will perform stretching and strengthing exercises only. Outcome measures will include pain intensity, foot functional disability , and static balance. The results of this study will provide evidence regarding the effectiveness of cognitive training with stretching and strengthing exercises compared to stretching and strengthIng only exercises in improving musculoskeletal function and balance.

Detailed Description

and impaired balance. It is characterized by degeneration of the plantar fascia due to repetitive stress, leading to pain, especially during weight-bearing activities. In addition to local tissue pathology, alterations in neuromuscular control and sensorimotor function may contribute to persistent symptoms and functional limitations.

Recent approaches in rehabilitation have highlighted the role of cognitive training in enhancing motor control, attention, and sensorimotor integration. Cognitive training, particularly when combined with movement tasks (dual-task training), may improve postural control and functional performance by optimizing central nervous system processing. However, there is limited evidence regarding its effectiveness in patients with plantar fasciitis.

This randomized controlled trial aims to investigate the effect of cognitive training on pain intensity, functional disability, and static balance in individuals with plantar fasciitis. Participants will be randomly assigned into two groups. The experimental group will receive a cognitive training program incorporating attention-demanding and dual-task exercises integrated with functional movements plus stretching and strengthing exercises . The control group will perform a conventional stretching and strengthing exercise program targeting the plantar fascia and related lower limb musculature.

Outcome measures will include pain intensity, functional disability, and static balance. Assessments will be conducted at baseline and after completion of the intervention period.

The results of this study are expected to provide evidence on the effectiveness of cognitive training as a rehabilitation approach for improving pain, functional outcomes, and balance in patients with plantar fasciitis.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Participant)

Masking Description

the participant don not know in which group and the type of treatment

Eligibility Criteria

Ages
18 Years to 60 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • 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.

Exclusion Criteria

  • 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.

Arms & Interventions

Cognitive Training Group

Experimental

Participants in this group will receive a structured cognitive training program integrated with functional movement tasks. The training will focus on improving attention, motor control, and sensorimotor integration through dual-task and task-oriented exercises designed to enhance postural control and functional stability. Sessions will be conducted over the intervention period with progressive difficulty based on participant performance.

Intervention: cognitive training (Behavioral)

Cognitive Training Group

Experimental

Participants in this group will receive a structured cognitive training program integrated with functional movement tasks. The training will focus on improving attention, motor control, and sensorimotor integration through dual-task and task-oriented exercises designed to enhance postural control and functional stability. Sessions will be conducted over the intervention period with progressive difficulty based on participant performance.

Intervention: stretching and strengthing exercises (Behavioral)

stretching and strengthing exercises

Experimental

Participants in this group will receive a conventional stretching and strengthing exercise program targeting the plantar fascia and related lower limb muscles. The exercises will focus on improving flexibility and reducing tissue tightness. Stretching will be performed in a standardized manner over the intervention period.

Intervention: stretching and strengthing exercises (Behavioral)

Outcomes

Primary Outcomes

Pain by VAS

Time Frame: at baseline and post treatment (4 weeks)

Pain intensity will be assessed using the Visual Analogue Scale (VAS), a 10 cm scale ranging from 0 (no pain) to 10 (worst imaginable pain). Participants will be asked to rate their current level of heel pain.

functional disability

Time Frame: at baseline and post treatment (4 weeks)

Functional disability will be assessed using the Foot Function Index (FFI), which evaluates pain, disability, and activity limitation in individuals with foot disorders. Higher scores indicate greater disability.

static balance

Time Frame: at baseline and post treatment ( 4 weeks)

Static balance will be assessed using a standardized balance test (e.g., single-leg stance test). Participants will be evaluated based on their ability to maintain a stable posture for a specified duration under controlled conditions.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Sahar Mowad Abdelmutilibe

Principal Investigator

Beni-Suef University

Study Sites (1)

Loading locations...

Similar Trials