AzTrials
AzTrials

Planter FasciitisCOG-PLANTNCT07571122

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

A study testing cognitive training and stretching and strengthing exercises in people with Planter Fasciitis, run by Beni-Suef University at 1 site in Egypt.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
Search all trials

Trial 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. Read more about this study

Who is it for?
Ages 18 to 60 years
Conditions the study is for
Planter Fasciitis
What is being tested?
cognitive training and stretching and strengthing exercises
Could I receive a placebo?
No, everyone receives an active treatment
How many people
80 participants
Where
1 siteEgypt
Study dates
3 Feb 2026to 25 May 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 60 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • 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.

Who cannot join

  • 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.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Sahar M Abdelmutilibe, PHD contact

0021027620061 ext. N/P

sahar.mowad@pt.bsu.edu.eg

Egypt1 site, 1 recruiting
  • Outpatient clinics of the Faculty of Physical Therapy, Beni Suef University

    Cairo

    Sahar M Abdelmutilibe, PHD, 0021027620061 ext. N/P, sahar.mowad@pt.bsu.edu.eg

    sahar m abdelmutilibe, PHD, 0021110374341 ext. N/P, saharmowad04@gmail.com

    Recruiting

Other trials in Egypt

About this study

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

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.

Read the 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.

Being tested
cognitive training, stretching and strengthing exercises
Keywords
Plantar Fasciitis, cognitive training, Heel Pain, stretching exercises, strengthIng exercises
Medical subject headings
Fasciitis, Plantar

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • cognitive trainingBehavioural

    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.

  • stretching and strengthing exercisesBehavioural

    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.

Study groups in NCT07571122
Study groupRoleWhat they receive
Cognitive Training GroupExperimentalParticipants 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.
Receives: Behavioral: cognitive training; Behavioral: stretching and strengthing exercises
stretching and strengthing exercisesExperimentalParticipants 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.
Receives: Behavioral: stretching and strengthing exercises

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Pain by VAS

    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.

    Measured: at baseline and post treatment (4 weeks)

  2. functional disability

    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.

    Measured: at baseline and post treatment (4 weeks)

  3. static balance

    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.

    Measured: at baseline and post treatment ( 4 weeks)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted6 May 2026
  2. Study start3 Feb 2026
  3. Primary completion4 May 2026 (estimated)
  4. Study completion25 May 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
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.
Masking
Single blind
Who is masked
Participant
Enrolment
80 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07571122
Sponsor's protocol ID
FPTBSURE/0112/15426
Other IDs
FPTBSURE/0112/15426
Acronym
COG-PLANT
Status last verified
Apr 2026
First submitted
30 Apr 2026
Last updated
6 May 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Individual participant data will not be shared due to privacy and confidentiality considerations. Data may be available upon reasonable request from the principal investigator and in accordance with institutional regulations.

Questions about this trial

What is this clinical trial studying?

A study testing cognitive training and stretching and strengthing exercises in people with Planter Fasciitis, run by Beni-Suef University at 1 site in Egypt.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 6 May 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Sahar M Abdelmutilibe, PHD (0021027620061 ext. N/P, sahar.mowad@pt.bsu.edu.eg), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Pain by VAS (time frame: at baseline and post treatment (4 weeks)). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 May 2026.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in