Pilates and Aerobic Training on Cardiorespiratory Fitness, Flexibility, Strength, and Muscular Power in Young Adults
1 other identifier
interventional
80
1 country
1
Brief Summary
Pilates exercises have been shown to be effective for a range of outcomes; however, it is unclear whether they can effectively contribute to improving cardiorespiratory fitness, especially when compared with aerobic training, which is known to be effective for this purpose. Furthermore, the differences between these modalities for outcomes such as flexibility, strength, and muscular power require further investigation. Therefore, the objective of this study is to assess the effectiveness of Pilates compared to aerobic training, as well as the combination of these activities, on cardiorespiratory fitness, flexibility, strength, and muscular power in young adults. Eighty women aged 18 to 40 will be randomized to four groups: Pilates (n = 20), aerobic (n = 20), Pilates plus aerobic (n = 20), and control (n = 20). Cardiorespiratory fitness will be assessed directly to estimate V̇O2max. Trunk flexibility in flexion and extension will be measured with a fleximeter (°). Lower-limb, upper-limb, and trunk muscle strength will be assessed by isokinetic dynamometry (N.m), while lower-limb muscle power (W) will be assessed by countermovement jumping on a force platform. Interventions will be conducted for 12 weeks, three times a week, with a 60-minute session duration. Analyses will be conducted by intention-to-treat and per-protocol.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Aug 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 30, 2025
CompletedFirst Posted
Study publicly available on registry
August 6, 2025
CompletedStudy Start
First participant enrolled
August 10, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 10, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 10, 2025
CompletedJanuary 8, 2026
January 1, 2026
4 months
July 30, 2025
January 7, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Cardiorespiratory Fitness
Maximum volume of oxygen obtained directly from inhaled and exhaled gases (V̇O2max) in a maximum incremental treadmill test.
Baseline and after 12 weeks
Secondary Outcomes (5)
Flexibility
Baseline and after 12 weeks
Trunk muscle strength
Baseline and after 12 weeks
Lower limb muscle strength
Baseline and after 12 weeks
Upper limb muscle strength
Baseline and after 12 weeks
Lower limb muscle power
Baseline and after 12 weeks
Study Arms (4)
Pilates
EXPERIMENTALA total of 13 exercises were selected for the Pilates group, including two stretching exercises and 11 strengthening exercises for the main muscle groups. Mat exercises and equipment exercises (Ladder Barrel, Cadillac, Step Chair, Reformer, Springboard, and Small Barrel) will be used. Two protocols will be adopted for progression (protocol 1: weeks 1-6; protocol 2: weeks 7-12). Two sets of 10 repetitions will be performed, with a 30-second rest between sets and exercises. The two-by-two rule will be used to increase the load. In this case, the load will increase when the participant performs ≥ 2 repetitions above their target of 10 repetitions in the last set, in two consecutive training sessions. The interventions will last 12 weeks, three times a week, for 60 minutes.
Aerobic
EXPERIMENTALThe aerobic group will perform walking/running exercises on a treadmill, using the extensive interval training method. To define the intensity and periodization of the training, the running speed associated with V̇O2max (vV̇O2max), second ventilatory threshold (vLV2), and average speed between vV̇O2max and vLV2 (v50%Δ) will be used as a reference. These parameters will be obtained from a maximal exercise test on a treadmill, performed before the start of the interventions. Two protocols will be adopted, with adjustments in density (work-to-recovery ratio) every two weeks. The interventions will last 12 weeks, three times a week, for 60 minutes.
Pilates plus aerobic
EXPERIMENTALThey will perform the same exercises as the Pilates group, however, with 1 set of 10 repetitions, with a 30-second rest between sets and exercises, totaling 30 minutes of intervention per session. In the second half of the intervention period, aerobic exercises will be performed, identical to those of the aerobic group, but for 30 minutes. The interventions will last 12 weeks, three times a week, for 60 minutes.
Control
NO INTERVENTIONThis group will be instructed to maintain their usual routine.
Interventions
Pilates exercises are characterized as muscle strengthening and stretching.
Aerobic exercises are characterized as a modality that works cardiorespiratory fitness.
Pilates exercises are characterized as muscle strengthening and stretching, while aerobic exercises are characterized as a modality that works cardiorespiratory fitness.
Eligibility Criteria
You may qualify if:
- female;
- age between 18 and 40 years; - not having exercised in the last 6 months;
- agreeing not to perform any other type of exercise during the study period;
- being fit to exercise according to the Physical Activity Readiness Questionnaire (PAR-Q) criteria;
- having no musculoskeletal or neurological disorders that could affect exercise performance;
- having no known cardiovascular or respiratory diseases;
- having no cognitive impairment that could lead to the inability to follow simple commands;
- not being a smoker;
- not being pregnant;
- not being on any specific diets.
You may not qualify if:
- refusing to sign the informed consent form;
- being unable to complete the pre-intervention assessment procedures.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Universidade Estadual do Norte do Paraná
Jacarezinho, Paraná, 86400-000, Brazil
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
July 30, 2025
First Posted
August 6, 2025
Study Start
August 10, 2025
Primary Completion
December 10, 2025
Study Completion
December 10, 2025
Last Updated
January 8, 2026
Record last verified: 2026-01
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- SAP
- Time Frame
- From September 1, 2025, until the date of publication of the study.
- Access Criteria
- The information will be freely accessible.
Individual participant data will be provided as supplementary material upon publication of the study results.