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Clinical Trials/NCT06817798
NCT06817798Not yet recruitingNot Applicable

Effects of Specific Foot Mobility Techniques on Biomechanical and Functional Parameters in Young Adults: a Randomized Controlled Trial

Cooperativa de Ensino Superior, Politécnico e Universitário1 site in 1 country60 target enrollmentStarted: February 1, 2025Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
60
Locations
1
Primary Endpoint
Balance - Y balance test

Study Overview

Brief 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)

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:

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
Double (Participant, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

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.

Arms & Interventions

Specific foot mobility

Experimental

Specific mobility of the foot, performed bilaterally.

Intervention: Specific foot mobility (Other)

Control

No Intervention

No intervention

Outcomes

Primary Outcomes

Balance - Y balance test

Time Frame: 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.

Navicular height - Navicular drop test

Time Frame: 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.

Baropodometric pressure

Time Frame: 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.

Anterior functional reach - functional reach test

Time Frame: 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.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Cooperativa de Ensino Superior, Politécnico e Universitário
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Maria Paço

Principal investigator

Cooperativa de Ensino Superior, Politécnico e Universitário

Study Sites (1)

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