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Cognitive Training for Pain , Balance and Foot Function in Plantar Fasciitis

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

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07571122
Acronym
COG-PLANT
Enrollment
80
Registered
2026-05-06
Start date
2026-02-03
Completion date
2026-05-25
Last updated
2026-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Planter Fasciitis

Keywords

Plantar Fasciitis, cognitive training, Heel Pain, stretching exercises, strengthIng exercises

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.

Interventions

BEHAVIORALcognitive training

Participants will receive a structured cognitive training program incorporating dual-task and task-oriented exercises. The intervention focuses on enhancing attention, motor planning, and sensorimotor integration during functional activities. Exercises are progressively advanced based on participant performance to improve postural control and functional stability.

BEHAVIORALstretching and strengthing exercises

Participants will perform a standardized stretching and strengthing program targeting the plantar fascia and associated lower limb muscles. The intervention consists of static stretching exercises aimed at improving tissue flexibility, reducing muscle tightness, and supporting pain reduction. Exercises will be performed in a controlled and consistent manner throughout the study period.

Sponsors

Beni-Suef University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Masking description

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

Intervention model description

This study is a two-arm parallel-group randomized controlled trial with equal allocation. Participants will be randomly assigned to either the cognitive training intervention or the stretching exercise intervention. No crossover between groups will occur. Both interventions will be delivered over the same duration, and outcome measures will be evaluated at baseline and after completion of the intervention period.

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
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.

Design outcomes

Primary

MeasureTime frameDescription
Pain by VASat 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 disabilityat 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 balanceat 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.

Countries

Egypt

Contacts

CONTACTSahar M Abdelmutilibe, PHD
sahar.mowad@pt.bsu.edu.eg0021027620061
PRINCIPAL_INVESTIGATORSahar M Abdelmutilibe, PHD

Faculty of Physical Therapy, Beni Suef University, Cairo, Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 7, 2026