- ICH GCP
- Register voor klinische proeven in de VS.
- Klinische proef NCT07632924
Medial Arch-Support Wrestling Shoes and Foot Posture Preservation in Adolescent Wrestlers (MAWS-RCT)
Medial Arch-Support Wrestling Shoes and Foot Posture Preservation in Adolescent Wrestlers: A Three-Year Randomized Controlled Trial
This three-year randomized controlled trial investigated whether wrestling shoes with built-in medial arch support can preserve foot arch structure in adolescent male wrestlers compared to standard wrestling shoes without arch support.
A total of 88 adolescent male wrestlers (age 11 at baseline) were randomly assigned to wear either modified wrestling shoes with integrated medial arch support (intervention group, n=44) or standard commercially available wrestling shoes (control group, n=44). Foot posture was assessed annually using the Staheli Arch Index via podoscopy. Plantar pressure distribution was recorded using the Tekscan F-Scan system. The study followed participants for three years.
The primary aim was to determine whether medial arch-support wrestling shoes reduce the emergence of flat foot (pes planus) compared with standard wrestling shoes during a critical period of foot development in young athletes.
Studie Overzicht
Toestand
Conditie
Interventie / Behandeling
Studietype
Inschrijving (Werkelijk)
Fase
- Niet toepasbaar
Contacten en locaties
Studie Locaties
-
-
-
Malatya, Turkije (Türkiye)
- Regional Boarding School (YBO)
-
-
Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Kind
Accepteert gezonde vrijwilligers
Beschrijving
Inclusion Criteria:
- Registered wrestlers at Regional Boarding Schools (YBO)
- Training frequency of 3 or more days per week
- No lower extremity injury within the preceding 6 months
- No current orthopedic insole use
- Normal foot posture at baseline
Exclusion Criteria:
- Prior lower extremity surgery
- Neurological disorders
- Rheumatological disorders
- Severe congenital foot deformity
- Current orthopedic insole use
- Existing foot deformity at baseline
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Preventie
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Enkel
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Experimenteel: Modified Wrestling Shoe (Arch Support)
Participants wore modified wrestling shoes with integrated medial arch support, multi-density rubber outsole, reinforced heel stabilization, structured midfoot midsole, and optimized plantar contact geometry for three years during all wrestling training sessions.
Shoe sizes were monitored and replaced as needed.
|
Modified wrestling shoe incorporating a multi-density rubber outsole, integrated medial longitudinal arch support, reinforced heel stabilization with hidden heel pads, structured midfoot midsole, four-way stretch Scuba fabric upper, and adhesive Velcro tape closure system.
Designed to redistribute plantar pressure and preserve medial longitudinal arch structure during wrestling training.
|
|
Actieve vergelijker: Standard Wrestling Shoe
Participants wore standard commercially available wrestling shoes featuring a flat thin rubber outsole, no cushioning midsole, no arch support, near-zero heel drop, and a high collar for three years during all wrestling training sessions.
Shoe sizes were monitored and replaced as needed.
|
Conventional commercially available wrestling shoe featuring a thin flat rubber outsole, hard insole without arch support, tight lacing system, high collar, and rigid non-flexible plastic base.
No medial arch support or plantar load redistribution features.
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Foot Posture Classification (Staheli Arch Index)
Tijdsspanne: Baseline, Year 1, Year 2, Year 3
|
Foot posture was classified annually using the Staheli Arch Index (SAI) assessed via podoscopy.
Classifications: normal (SAI 0.45-0.89),
flexible pes planus (SAI 0.90-1.00),
and rigid pes planus (SAI ≥1.01, confirmed by Jack Toe Raise Test).
Between-group differences were evaluated using Fisher's exact test with Bonferroni correction.
|
Baseline, Year 1, Year 2, Year 3
|
Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Plantar Pressure Distribution
Tijdsspanne: Year 3
|
Dynamic plantar pressure distribution was recorded using the Tekscan F-Scan system (3000E sensors, 100 Hz) during 30-second walking trials on a UWW-approved mat.
Pressure maps were evaluated qualitatively for midfoot contact area and center of pressure trajectory.
|
Year 3
|
|
Standing Height
Tijdsspanne: Baseline, Year 1, Year 2
|
Standing height (cm) was measured using a calibrated stadiometer at each assessment point.
Between-group differences were analyzed using mixed-design ANOVA (group × time).
|
Baseline, Year 1, Year 2
|
|
Body Mass
Tijdsspanne: Baseline, Year 1, Year 2
|
Body mass (kg) was measured using a calibrated scale at each assessment point.
Between-group differences were analyzed using mixed-design ANOVA (group × time).
|
Baseline, Year 1, Year 2
|
Medewerkers en onderzoekers
Sponsor
Onderzoekers
- Hoofdonderzoeker: Mahmut Açak, Çanakkale Onsekiz Mart University
Studie record data
Bestudeer belangrijke data
Studie start (Werkelijk)
Primaire voltooiing (Werkelijk)
Studie voltooiing (Werkelijk)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Aanvullende relevante MeSH-voorwaarden
- Talipes
- Musculoskeletale aandoeningen
- Musculoskeletale afwijkingen
- Aangeboren afwijkingen
- Misvormingen van de onderste ledematen, aangeboren
- Misvormingen van ledematen, aangeboren
- Voetmisvormingen, verworven
- Voetmisvormingen, aangeboren
- Aangeboren, erfelijke en neonatale ziekten en afwijkingen
- Voetafwijkingen
- Platte voet
Andere studie-ID-nummers
- 2018-106
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .