Cooperativa de Ensino Superior, Politécnico e Universitário
Phase
Not applicable
Started
2025-02
Last updated
2025-02-10
Condition(s) studied
Healthy
Investigational drug(s) / intervention(s)
Specific foot mobility
Specific foot mobility: Specific mobility of the foot, performed bilaterally.
Study summary
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)
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
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.
Primary outcome measure(s)
Balance - Y balance test — M0: Before intervention; M1: Immediately after intervention; M2: 24h after intervention. Assesses dynamic balance by having participants reach as far as possible in multiple directions with one foot while maintaining balance on the other, providing insight into lower limb stability and control.
Baropodometric pressure — M0: Before intervention; M1: Immediately after intervention; M2: 24h after intervention. To assess load distribution, participants will be instructed to stand on the force platform in an orthostatic position for 30 seconds.
Navicular height - Navicular drop test — M0: Before intervention; M1: Immediately after intervention; M2: 24h after intervention. The navicular drop test will be performed. In this test, the height of the navicular bone is measured with a caliper (in millimetres) from the ground to the most distal point of this bone.
Anterior functional reach - functional reach test — M0: Before intervention; M1: Immediately after intervention; M2: 24h after intervention. The participant is instructed to stand close to, but not touching, a wall and position the arm that is closer to the wall at 90 degrees of shoulder flexion with a closed fist. The assessor records the starting position at the 3rd metacarpal head on the yardstick. Then, the participant is instructed to "Reach as far as you can forward without taking a step." The location of the 3rd metacarpal is then recorded in this position. The difference between the start and end position is the reach distance.
Trial sites (1)
Facility
City
Region
Status
Escola Superior de Saúde do Vale do Ave
Vila Nova de Famalicão
Braga District
More Cooperativa de Ensino Superior, Politécnico e Universitário trials in Portugal
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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