Impact of Foot Mobility Techniques on Balance and Pressure in Young Adults
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Specific foot mobility.
- Who it may be relevant to
- Registry conditions: Healthy. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Portugal
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Effects of Specific Foot Mobility Techniques on Biomechanical and Functional Parameters in Young Adults: A Randomized Controlled Trial
Overview
This study aims to evaluate the effectiveness of specific foot mobility techniques on functional and biomechanical parameters of the foot in young adults aged 18 to 24 years. The study employs a randomized controlled trial design with the following key components: Key outcomes include: Baropodometric pressures (measured using a baropodometric platform). Balance (evaluated through the Y-Balance Test). Navicular height (assessed using the Navicular Drop Test) Anterior functional reach (measured through functional reach test)
Detailed description
This study explores the immediate and short-term effects of specific foot mobility techniques on functional and biomechanical outcomes in healthy young adults. The research is grounded in the growing recognition of the foot's critical role in postural control, balance, and lower-limb biomechanics.
The intervention consists of foot mobility techniques designed to improve joint mobility and overall foot function. These techniques will be applied bilaterally. The study employs a randomized controlled trial design, with participants randomly allocated to either the experimental group (receiving the intervention) or the control group (receiving no treatment during the intervention period).
Participants are assessed at three time points:
Baseline (M0): Before the intervention. Immediately Post-Intervention (M1). Follow-Up (M2): 24 hours after the intervention.
The primary outcomes include:
Changes in plantar pressure distribution and postural control as measured by a baropodometric platform.
Balance performance assessed through the Y-Balance Test. Navicular height variation evaluated using the Navicular Drop Test. Anterior functional reach, measured by Functional Reach Test. The study focuses on identifying measurable improvements in functional and biomechanical parameters that may enhance clinical approaches to foot health and rehabilitation. By targeting a young and healthy population, the research aims to establish a foundation for further studies in other age groups and clinical conditions. This work aims to contribute to evidence-based practices in manual therapy and foot biomechanics.
Interventions
- Other Specific foot mobility
Specific mobility of the foot, performed bilaterally.
Primary outcome measures
- Balance - Y balance test [Time frame: M0: Before intervention; M1: Immediately after intervention; M2: 24h after intervention.]
- Baropodometric pressure [Time frame: M0: Before intervention; M1: Immediately after intervention; M2: 24h after intervention.]
- Navicular height - Navicular drop test [Time frame: M0: Before intervention; M1: Immediately after intervention; M2: 24h after intervention.]
- Anterior functional reach - functional reach test [Time frame: M0: Before intervention; M1: Immediately after intervention; M2: 24h after intervention.]
Eligibility criteria
Inclusion criteria
- minimum age of 18 years.
Exclusion criteria
- pregnant women,
- individuals with lesions in the lower limbs in the last 12 months,
- history of congenital deformity in the lower limb
- presence of vestibular or balance disorders
- users of corrective insoles or orthoses.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Double blind
- Primary purpose
- Other
Study locations
Portugal · 1 center
- Escola Superior de Saúde do Vale do Ave — Vila Nova de Famalicão
Identifiers
NCT: NCT06817798 · Foot mobility_2025