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PILATES AND AEROBIC TRAINING ON BODY COMPOSITION IN YOUNG ADULTS

U

Universidade Estadual do Norte do Parana

Status

Completed

Conditions

Improved Body Composition

Treatments

Other: Pilates exercises plus aerobic exercise
Other: Pilates exercises
Other: Aerobic exercise

Study type

Interventional

Funder types

Other

Identifiers

NCT07107061
GPASD_001_2025

Details and patient eligibility

About

Pilates exercises have been shown to be effective for a range of outcomes; however, it is unclear whether they can effectively contribute to fat mass reduction, especially when compared with a technique known to be effective for this purpose, such as aerobic training. Furthermore, Pilates' potential for increasing lean mass also requires further investigation. The aim of this study was to assess the effectiveness of Pilates compared with aerobic training, as well as the combination of these activities, on body composition in young adults. Eighty women aged 18 to 40 years were randomized to four groups: Pilates (n = 20), aerobic (n = 20), Pilates plus aerobic (n = 20), and control (n = 20). Body composition was assessed by dual-energy X-ray absorptiometry (DXA), considering: total fat mass (kg), percentage of total fat mass (%), total lean mass (kg), and total lean mass adjusted for height (kg/m²). Additionally, total body mass (kg) and body mass index (BMI) (kg/m2) values were considered. The interventions were carried out for 12 weeks, three times a week, lasting 60 minutes/session. Analyses were performed by intention-to-treat and per protocol.

Enrollment

80 patients

Sex

Female

Ages

18 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 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;
  • Not having musculoskeletal or neurological disorders that could affect exercise performance;
  • Not having known cardiovascular or respiratory diseases;
  • Not having cognitive impairment that leads to the inability to follow simple commands;
  • Not being a smoker;
  • Not being pregnant;
  • Not being on any specific diets.

Exclusion criteria

  • Refusing to sign the informed consent form;
  • Unable to complete the pre-intervention assessment procedures.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

80 participants in 4 patient groups

Pilates
Experimental group
Description:
A 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.
Treatment:
Other: Pilates exercises
Aerobic
Experimental group
Description:
The 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 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.
Treatment:
Other: Aerobic exercise
Pilates plus aerobic
Experimental group
Description:
They 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.
Treatment:
Other: Pilates exercises plus aerobic exercise
Control
No Intervention group
Description:
This group will be instructed to maintain their usual routine.

Trial contacts and locations

1

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Central trial contact

Raphael G Oliveira, PhD

Data sourced from clinicaltrials.gov

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