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Effects of Stabilization-based Pilates Exercise on Gait and Balance in Women With Flexible Pesplanus

NCT06583434 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 22

Last updated 2024-09-19

No results posted yet for this study

Summary

The goal of this clinical trial was to determine if stabilization-based Pilates exercises could improve gait and balance in women with flexible flatfoot.

The main questions it aimed to answer were:

Did Pilates training improve gait parameters in women with flexible flatfoot? Did Pilates training reduce balance instability in these participants?

Researchers compared the Pilates training group to a non-training group. The results showed significant improvements in gait and balance for those who participated in the Pilates training.

Participants:

Completed twice-weekly Pilates sessions for 8 weeks. Underwent pre- and post-intervention assessments of gait and balance.

Conditions

  • Flexible Flatfoot

Interventions

BEHAVIORAL

core-lower extremity Pilates Training Group

Participants in this group will engage in a stabilization-based Pilates exercise program focusing on core and lower extremity stabilization. The program consists of twice-weekly sessions, each lasting 50 minutes, over a period of 8 weeks. The primary goal of the intervention is to improve gait patterns and balance in women with flexible pes planus

OTHER

Non-Training Group

Participants in this group will not receive any specific intervention during the study period. They will continue their usual activities without any additional exercises provided by the study.

Sponsors & Collaborators

  • Hyun Ju Kim

    lead OTHER

Principal Investigators

  • Hyun Ju Kim, MSc · Department of Sports and Health Convergence

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-01-02
Primary Completion
2024-03-08
Completion
2024-03-30

Countries

  • South Korea

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06583434 on ClinicalTrials.gov