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Immediate Effects of Plantar Fascia Release Combined With Foot Exercises on FMS Subscores in Young Adults With Pes Planus (FMS-PP)

24 de junio de 2026 actualizado por: Emre Serdar Atalay, Sultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey

Immediate Effects of Plantar Fascia Release Combined With Foot Exercises on Functional Movement Screen Subscores in Young Adults With Pes Planus: A Randomized Crossover Study

This randomized crossover clinical study aims to investigate the immediate effects of plantar fascia release combined with foot exercises on Functional Movement Screen sub-scores in physically active young adults with pes planus.

Participants aged 18-35 years with pes planus, determined by the Navicular Drop Test, will complete two different intervention protocols in a randomized order. Protocol A will include foot-core exercises combined with plantar fascia stretching. Protocol B will include the same foot-core exercises and plantar fascia stretching, with the addition of plantar fascia myofascial release. Each participant will receive both interventions on separate sessions, with a 24-hour washout period between sessions.

Functional movement quality will be assessed using two Functional Movement Screen subtests: Deep Squat and Hurdle Step. These tests will be performed before and after each intervention session to evaluate acute changes in movement performance.

The main hypothesis of the study is that plantar fascia myofascial release combined with foot-core exercises and plantar fascia stretching will produce greater immediate improvements in Functional Movement Screen Deep Squat and Hurdle Step scores compared with foot-core exercises and plantar fascia stretching alone.

Descripción general del estudio

Descripción detallada

This study is planned as a randomized crossover interventional clinical study designed to evaluate the acute effects of plantar fascia release combined with foot exercises on functional movement quality in young adults with pes planus.

Pes planus is associated with reduced medial longitudinal arch support and excessive pronation, which may influence lower extremity alignment, load transfer, postural control, and functional movement patterns. Foot-core exercises aim to activate and strengthen the intrinsic muscles of the foot that support the medial longitudinal arch. Plantar fascia stretching and myofascial release may improve the flexibility and mechanical properties of the plantar fascia and may contribute to improved ankle and lower extremity movement capacity. Therefore, combining active foot stabilization exercises with plantar fascia interventions may provide an immediate effect on movement quality.

The study will include physically active young adults aged 18-35 years with pes planus. Pes planus will be determined using the Navicular Drop Test. Physical activity level will be assessed using the International Physical Activity Questionnaire. After eligibility screening and written informed consent, participants will complete two different intervention protocols in a randomized order.

The crossover design will allow each participant to receive both intervention protocols and serve as their own control. A 24-hour washout period will be provided between the two intervention sessions to minimize possible carryover effects. In each session, Functional Movement Screen subtests will be assessed before the intervention. The assigned intervention protocol will then be applied, followed by a one-hour waiting period. After this waiting period, the Functional Movement Screen subscores will be repeated to determine the immediate effect of the intervention.

Protocol A will consist of foot-core exercises combined with plantar fascia stretching. The foot-core exercise program will include short foot exercise, towel curl, toe spread, great toe extension, and reverse tandem walking. Plantar fascia stretching will be performed using a plantar fascia-specific stretching technique.

Protocol B will consist of the same foot-core exercises and plantar fascia stretching, with the addition of plantar fascia myofascial release. Myofascial release will be applied manually along the plantar fascia, from the calcaneal region toward the metatarsal heads, with controlled pressure and within the participant's tolerance.

Functional movement quality will be evaluated using the Deep Squat and Hurdle Step subtests of the Functional Movement Screen. These tests were selected because they reflect lower extremity mobility, stability, balance, and movement control, which may be influenced by foot posture and plantar fascia mobility.

The primary aim of the study is to compare the immediate effects of the two intervention protocols on Functional Movement Screen Deep Squat and Hurdle Step scores. The study hypothesis is that the protocol including plantar fascia myofascial release, plantar fascia stretching, and foot-core exercises will result in greater immediate improvement in Functional Movement Screen subscores compared with foot-core exercises and plantar fascia stretching alone.

All assessments and interventions will be performed face to face in a clinical setting by trained physiotherapists. Procedures will be conducted according to standardized instructions, and participant safety and comfort will be monitored throughout the study.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

29

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

Copia de seguridad de contactos de estudio

Ubicaciones de estudio

    • Ankara
      • Ankara, Ankara, Turquía (Türkiye), 06018
        • University of Healt Sciences, Gülhane Faculty ofHealth Sciences

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto

Acepta Voluntarios Saludables

No

Descripción

Inclusion Criteria:

  • Being between 18 and 35 years of age
  • Voluntarily agreeing to participate in the study and providing written informed consent
  • Having pes planus according to the Navicular Drop Test result
  • Having the cognitive ability to understand and perform the Functional Movement Screen (FMS) test instructions
  • Being classified as sufficiently physically active according to the International Physical Activity Questionnaire (IPAQ), defined as at least 1,500 MET-min/week of vigorous-intensity activity or at least 3,000 MET-min/week of moderate-intensity activity
  • Having no history of lower-extremity surgery within the previous 6 months
  • Having no history of lower-extremity injury or disability within the previous 6 months
  • Agreeing to complete the study protocol over two days

Exclusion Criteria:

  • Having a history of ankle sprain, particularly recurrent ankle sprains
  • Presence of hallux valgus deformity
  • Presence of hammer toe deformity
  • Presence of generalized ligamentous laxity
  • Having a history of systemic disease, such as rheumatic, neurological, or metabolic disorders
  • Presence of ongoing lower-extremity pain
  • Having any orthopedic or neurological condition that may prevent the safe performance of the Functional Movement Screen tests

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Prevención
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación cruzada
  • Enmascaramiento: Único

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Protocol A
Participants will receive Protocol A, which includes foot core exercises combined with plantar fascia stretching. In the randomized crossover design, Protocol A may be administered either in the first session or in the second session, depending on the randomized intervention order. FMS Deep Squat and Hurdle Step scores will be assessed before and after the intervention session.
Protocol A consists of foot core exercises combined with plantar fascia stretching. Foot core exercises include short foot exercise, towel curl, toe spread, great toe extension, and reverse tandem walking. Plantar fascia stretching will be performed using a plantar fascia-specific stretching technique. This protocol may be administered in either the first or second session according to the randomized crossover order.
Experimental: Protocol B
Participants will receive Protocol B, which includes foot core exercises combined with plantar fascia stretching and plantar fascia myofascial release. In the randomized crossover design, Protocol B may be administered either in the first session or in the second session, depending on the randomized intervention order. FMS Deep Squat and Hurdle Step scores will be assessed before and after the intervention session.
Protocol B consists of all components of Protocol A, including foot core exercises and plantar fascia stretching, with the addition of plantar fascia myofascial release. Myofascial release will be applied manually along the plantar fascia from the calcaneal region toward the metatarsal heads, with pressure adjusted according to participant tolerance. This protocol may be administered in either the first or second session according to the randomized crossover order.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Change in Functional Movement Screen Hurdle Step Score
Periodo de tiempo: Before intervention and 1 hour after intervention in each session
The Hurdle Step subtest of the Functional Movement Screen will be used to assess single-leg balance, hip stability, knee control, and ankle stability. Scores ranges from 0 to 3, with higher scores indicating better movement quality. The change from pre-intervention to post-intervention will be compared between protocols.
Before intervention and 1 hour after intervention in each session
Change in Functional Movement Screen Deep Squat Score
Periodo de tiempo: Before intervention and 1 hour after intervention in each session
The Deep Squat subtest of the Functional Movement Screen will be used to assess functional movement quality involving the lower extremities, trunk, shoulders, hips, knees, and ankles. Scores range from 0 to 3, with higher scores indicating better movement quality. The change from pre-intervention to post-intervention will be compared between protocols.
Before intervention and 1 hour after intervention in each session

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Publicaciones y enlaces útiles

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Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Estimado)

18 de julio de 2026

Finalización primaria (Estimado)

14 de agosto de 2026

Finalización del estudio (Estimado)

14 de agosto de 2026

Fechas de registro del estudio

Enviado por primera vez

17 de junio de 2026

Primero enviado que cumplió con los criterios de control de calidad

17 de junio de 2026

Publicado por primera vez (Actual)

24 de junio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

29 de junio de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

24 de junio de 2026

Última verificación

1 de junio de 2026

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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