Cognitive Training for Pain , Balance and Foot Function in Plantar Fasciitis (COG-PLANT)
Effect of Cognitive Training on Pain , Foot Function, and Balance in Patients With Planter Fasciitis : A Randomized Controlled Trial
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
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.
Type d'étude
Inscription (Estimé)
Phase
- N'est pas applicable
Contacts et emplacements
Coordonnées de l'étude
- Nom: Sahar M Abdelmutilibe, PHD
- Numéro de téléphone: N/P 0021027620061
- E-mail: sahar.mowad@pt.bsu.edu.eg
Lieux d'étude
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Cairo, Egypte
- Recrutement
- Outpatient clinics of the Faculty of Physical Therapy, Beni Suef University
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Contact:
- Sahar M Abdelmutilibe, PHD
- Numéro de téléphone: N/P 0021027620061
- E-mail: sahar.mowad@pt.bsu.edu.eg
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Contact:
- sahar m abdelmutilibe, PHD
- Numéro de téléphone: N/P 0021110374341
- E-mail: saharmowad04@gmail.com
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Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
Accepte les volontaires sains
La description
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.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Seul
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
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Expérimental: Cognitive Training Group
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.
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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.
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.
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Expérimental: stretching and strengthing exercises
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.
|
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.
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Pain by VAS
Délai: at baseline and post treatment (4 weeks)
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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.
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at baseline and post treatment (4 weeks)
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functional disability
Délai: at baseline and post treatment (4 weeks)
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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.
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at baseline and post treatment (4 weeks)
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static balance
Délai: at baseline and post treatment ( 4 weeks)
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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.
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at baseline and post treatment ( 4 weeks)
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Collaborateurs et enquêteurs
Parrainer
Les enquêteurs
- Chercheur principal: Sahar M Abdelmutilibe, PHD, Faculty of Physical Therapy, Beni Suef University, Cairo, Egypt
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- FPTBSURE/0112/15426 (Identificateur de registre: faculty of physical therapy , Beni- Suef University)
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Description du régime IPD
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Étudie un produit d'appareil réglementé par la FDA américaine
produit fabriqué et exporté des États-Unis.
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