The Role of Focus Strategies on Pilates

December 18, 2025 updated by: Ayça Araci, Alanya Alaaddin Keykubat University

The Role of Focus Strategies on Pilates Performance and Reaction Time: A Randomized Controlled Trial

Aims of the randomized controlled study is compare to the effects of external and internal focus strategies, commonly used in Pilates, on participants' reaction time and performance metrics. Conducted over an 8-week Pilates program at Alanya Alaaddin Keykubat University, we plan to include 25 participants in each focus group. Participants in the external focus group will use equipment to perform exercises, while the internal focus group will perform exercises with attention to body positioning.

Study Overview

Detailed Description

The primary aim of this study is to examine the difference in effects between 8-week internally and externally focused Pilates exercises on the performance of young sedentary individuals. A secondary aim is to investigate the effects of internally and externally focused Pilates exercises on the physical characteristics and reaction time of young sedentary individuals.

Study Type

Interventional

Enrollment (Actual)

50

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Alanya
      • Antalya, Alanya, Turkey (Türkiye), 07450
        • Alanya Alaaddin Keykubat University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Volunteers aged between 18 and 30 years who have no musculoskeletal disabilities and are willing to exercise were included in the study.

Exclusion Criteria:

  • Had any cardiovascular or musculoskeletal condition that would prevent them from exercising,
  • Had an acute pain history of 5 or more on the visual analog scale in the past week,
  • Had a systemic disease that would prevent exercise,
  • Had a BMI of 30 or above,
  • Had any issues that would hinder their ability to perceive or understand verbal commands, or had hearing problems.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Supportive Care
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: External Focused Pilates
Pilates training was implemented with an external focus (EF).
Pilates training was implemented with an internal focus (IF).
Pilates training was implemented with an external focus (EF).
Experimental: Internal Focused Pilates
Pilates training was implemented with an internal focus (IF).
Pilates training was implemented with an internal focus (IF).
Pilates training was implemented with an external focus (EF).

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Multiple Jump Test
Time Frame: Baseline - right after the intervention
15-Second Continuous Jump Test
Baseline - right after the intervention
BFS Vertical Jump Test
Time Frame: Baseline - right after the intervention
The Vertical Jump Test is a practical test that provides information about an individual's anaerobic power level.
Baseline - right after the intervention
Squat Jump Test
Time Frame: Baseline - right after the intervention
The explosive strength characteristic demonstrated by the leg muscles is measured based on their maximal force.
Baseline - right after the intervention
Acoustic Reaction Test
Time Frame: Baseline - right after the intervention
This test measures the time between a visual/auditory stimulus and the athlete's response movement.
Baseline - right after the intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

October 5, 2024

Primary Completion (Actual)

April 15, 2025

Study Completion (Actual)

May 30, 2025

Study Registration Dates

First Submitted

November 9, 2024

First Submitted That Met QC Criteria

November 9, 2024

First Posted (Actual)

November 12, 2024

Study Record Updates

Last Update Posted (Actual)

December 24, 2025

Last Update Submitted That Met QC Criteria

December 18, 2025

Last Verified

December 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • 09.11.2024

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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