Denne siden ble automatisk oversatt og nøyaktigheten av oversettelsen er ikke garantert. Vennligst referer til engelsk versjon for en kildetekst.

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

24. juni 2026 oppdatert av: 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.

Studieoversikt

Detaljert beskrivelse

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.

Studietype

Intervensjonell

Registrering (Antatt)

29

Fase

  • Ikke aktuelt

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studer Kontakt Backup

Studiesteder

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

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Voksen

Tar imot friske frivillige

Nei

Beskrivelse

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

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Forebygging
  • Tildeling: Randomisert
  • Intervensjonsmodell: Crossover-oppdrag
  • Masking: Enkelt

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: 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.
Eksperimentell: 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.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Change in Functional Movement Screen Hurdle Step Score
Tidsramme: 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
Tidsramme: 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

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

18. juli 2026

Primær fullføring (Antatt)

14. august 2026

Studiet fullført (Antatt)

14. august 2026

Datoer for studieregistrering

Først innsendt

17. juni 2026

Først innsendt som oppfylte QC-kriteriene

17. juni 2026

Først lagt ut (Faktiske)

24. juni 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

29. juni 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

24. juni 2026

Sist bekreftet

1. juni 2026

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

Abonnere