Effects of Pilates Stretching on Flexibility, Strength, Power and Muscular Endurance

August 3, 2023 updated by: Raphael Goncalves de Oliveira, Universidade Estadual do Norte do Parana

Effects of Stretching in a Conditioning Program Based on Pilates Exercises on Flexibility, Strength, Power and Muscular Endurance

Introduction: The practice of stretching is commonly used in the preparation of activities and/or physical exercises that require some component of flexibility, strength, endurance and muscle power. This explains the high growth in recent decades of studies investigating the effect of stretching, mainly static and dynamic, when performed immediately before activities that aim to develop these physical capacities. Despite the growing interest of scholars on this topic, the long-term impact of dynamic stretching on flexibility, strength performance, endurance and muscle power is still not fully understood. In addition, a type of dynamic stretching little explored in the literature needs investigation: the stretches used during Pilates exercise sessions. The effects of these stretching exercises on a physical conditioning program based on Pilates exercises in the young adult population are not yet known. Objective: To verify through a randomized clinical trial the effects of stretching in a conditioning program based on Pilates exercises on flexibility, strength, endurance and muscle power. Methods: In this study, 32 young adults of both sexes will be randomized into two groups: 1) Traditional Pilates; 2) Pilates Without Stretching. The Traditional Pilates group will perform a protocol of stretching exercises followed by muscle strengthening. The Pilates Without Stretching group will perform an exercise protocol consisting only of muscle strengthening exercises. Muscle strength results will be evaluated by 1 repetition max by elastic resistance; trunk muscle strength/endurance by the 1-minute abdominal test and the Sorensen test, respectively; vertical jump performance by the sargent jump test; handgrip strength by the handheld dynamometer and flexibility by the sit-and-reach test. These physical capacities will be assessed at baseline and after 8 weeks of intervention. Interventions will be performed three times a week for 8 weeks. The analysis will be performed with intent-to-treat analysis and adjusted covariance for baseline outcomes.

Study Overview

Study Type

Interventional

Enrollment (Actual)

32

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

    • Paraná
      • Jacarezinho, Paraná, Brazil, 86400-000
        • Universidade Estadual do Norte do Paraná

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

18 years to 45 years (Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • women between 18 and 45 years of age
  • normoweights (Body mass index between 21 to 25 kg/m2)
  • not be participating in physical exercise programs for at least six months
  • be healthy, according to the Physical Activity Readiness Questionnaire
  • not report any medical restrictions for physical exercise
  • no history of injury, trauma or illness within the last six months
  • not having undergone previous surgery in the last six months
  • not have musculoskeletal, cardiorespiratory and neurological disorders that prevent the performance of assessment and intervention protocols
  • not be under the action of medications that cause muscle relaxation or that can inhibit muscle tonic action
  • not use food supplements or anabolic steroids
  • not being on a calorie-restricted diet

Exclusion Criteria:

  • start practicing another type of physical exercise during the study period
  • not being able to perform the pre-intervention assessment or the intervention exercise protocol
  • emergence of lesions that do not allow the continuity of interventions
  • withdraw from participating in the study

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: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Traditional Pilates

5 stretching exercises will be performed, followed by 15 strengthening exercises (5 for core, 5 for lower limbs and 5 for upper limbs), all in a series of 10 repetitions, 3x-week, for 8 weeks, maintaining an effort level 7-8 on the Omni-Scale. Below are the exercises and equipment used.

1) Stretching the Chain Posterior (Reformer); 2) Front Splits Modified (Reformer); 3) Stomach Massage (Reformer); 4) Stretches Front (Barrel); 5) Back Stretches: Quadriceps Stretch (Barrel); 6) Bridge (Mat with Magic Circle); 7) The Hundred (Mat with Swiss ball); 8) Teaser (Mini Barrel); 9) Swan (Mini Barrel); 10) Swimming (Mini Barrel); 11) Footwork Double Leg Pumps (Chair); 12) Pump One Leg Front (Chair); 13) Forward Lunge (Chair); 14) Wall Side (Wall with Swiss ball and dumbbells); 15) Tower (Cadillac); 16) Arms Pulling Up (Cadillac); 17) Rowing Front: Hug a Tree (Cadillac); 18) Arm Pulling Down (Wall Unit); 19) Horizontal Arm Pulling (Wall Unit); 20) Extension Arm Up (Wall Unit).

This group will perform a traditional Pilates session, which consists of stretching exercises, followed by exercises to strengthen the core (trunk flexors and extensors), lower limbs and upper limbs. The total duration of the intervention in this group should be approximately 50 minutes.
Experimental: Pilates without stretching

15 strengthening exercises will be performed (the same performed by the TP group), all in a series of 10 repetitions, 3x-week, for 8 weeks, maintaining an effort level 7-8 on the Omni-Scale. Below are the exercises and equipment used.

1) Bridge (Mat with Magic Circle); 2) The Hundred (Mat with Swiss ball); 3) Teaser (Mini Barrel); 4) Swan (Mini Barrel); 5) Swimming (Mini Barrel); 6) Footwork Double Leg Pumps (Chair); 7) Pump One Leg Front (Chair); 8) Forward Lunge (Chair); 9) Wall Side (Wall with Swiss ball and dumbbells); 10) Tower (Cadillac); 11) Arms Pulling Up (Cadillac); 12) Rowing Front: Hug a Tree (Cadillac); 13) Arm Pulling Down (Wall Unit); 14) Horizontal Arm Pulling (Wall Unit); 15) Extension Arm Up (Wall Unit).

This group will conduct a non-traditional Pilates session. This is because stretching exercises will be excluded. The muscle strengthening exercises will be the same as in the TP group, so that it is possible to discuss the influence of the inclusion/exclusion of stretching for the considered outcomes. The total duration of the intervention in this group should be approximately 35 minutes.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in strength/endurance by 1-minute sit-up test
Time Frame: Pre (baseline) and post-intervention assessment (after 8-weeks)
Assessment of abdominal muscle strength/endurance in 1-minute
Pre (baseline) and post-intervention assessment (after 8-weeks)
Change in muscle strength by handgrip test using hand dynamometer
Time Frame: Pre (baseline) and post-intervention assessment (after 8-weeks)
Assessment of handgrip muscle strength
Pre (baseline) and post-intervention assessment (after 8-weeks)
Change in the muscular resistance of the trunk extensors by the Sorensen test
Time Frame: Pre (baseline) and post-intervention assessment (after 8-weeks)
Assessment of the muscular resistance of the trunk extensors (Sorensen)
Pre (baseline) and post-intervention assessment (after 8-weeks)
Change in muscle strength of knee extensors
Time Frame: Pre (baseline) and post-intervention assessment (after 8-weeks)
Assessment of muscle strength with elastic resistance
Pre (baseline) and post-intervention assessment (after 8-weeks)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Lower limb muscle power
Time Frame: Pre (baseline) and post-intervention assessment (after 8-weeks)
Assessment of lower limb muscle power by vertical jump
Pre (baseline) and post-intervention assessment (after 8-weeks)
Flexibility
Time Frame: Pre (baseline) and post-intervention assessment (after 8-weeks)
Flexibility assessment by the sit-and-reach test
Pre (baseline) and post-intervention assessment (after 8-weeks)

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)

September 5, 2022

Primary Completion (Actual)

November 25, 2022

Study Completion (Actual)

November 25, 2022

Study Registration Dates

First Submitted

September 6, 2022

First Submitted That Met QC Criteria

September 9, 2022

First Posted (Actual)

September 14, 2022

Study Record Updates

Last Update Posted (Actual)

August 8, 2023

Last Update Submitted That Met QC Criteria

August 3, 2023

Last Verified

August 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • Pilates_stretching

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Data regarding the study will be shared in the publication linked to this record, as a main part of the manuscript and supplementary documents when necessary.

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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