- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06683898
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
Status
Completed
Intervention / Treatment
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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