Effects of 12 weeks of interval block resistance training versus circuit resistance training on body composition, performance and autonomic recovery in adults.

ISRCTN ISRCTN17853333
DOI https://doi.org/10.1186/ISRCTN17853333
Submission date
02/02/2025
Registration date
04/02/2025
Last edited
16/04/2025
Recruitment status
No longer recruiting
Overall study status
Completed
Condition category
Other
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Record updated in last year

Plain English summary of protocol

Background and study aims
This study is looking at two types of strength exercises, block training and circuit training, to see how they affect body shape, muscle strength, fitness levels, and recovery in young adults. The goal is to find out which type of exercise is better for improving health and physical performance.

Who can participate?
Physically active adults who are willing to take part in a 12-week exercise program can participate in this study.

What does the study involve?
Participants will be randomly assigned to either block training or circuit training groups. They will follow their assigned exercise program for 12 weeks. Before and after the program, participants will have their body composition measured (using body mass index and waist circumference), muscle strength tested (using a hand grip dynamometer), fitness levels assessed (using the 6-minute walk test), and movement speed evaluated (using a running anaerobic sprint test).

What are the possible benefits and risks of participating?
Participants may benefit from improved fitness, muscle strength, and body composition. However, as with any exercise program, there is a risk of injury. The study will be conducted under professional supervision to minimize these risks.

Where is the study run from?
The study will be conducted at the Municipal Stadium in Pirque, Chile.

When is the study starting and how long is it expected to run for?
January 2025 to April 2025

Who is funding the study?
Investigator initiated and funded

Who is the main contact?
Hector Fuentes-Barria, hefuentes_@unap.cl

Contact information

Mr Héctor Fuentes Barria
Public, Scientific, Principal Investigator

Avda. Arturo Prat 2120
Santiago
8150000
Chile

ORCiD logoORCID ID 0000-0003-0774-0848
Phone +56 996702455
Email hefuentes_@unap.cl

Study information

Study designInterventional randomized controlled double-blind trial
Primary study designInterventional
Secondary study designRandomised controlled trial
Study setting(s)Fitness/sport facility
Study typeDiagnostic
Participant information sheet 46785 PIS.pdf
Scientific titleEffects of block versus circuit resistance exercise on body composition and performance in adults. Randomized controlled trial
Study objectivesAre there significant differences in physical activity levels, body composition, muscle strength, functional capacity, sprint performance, and recovery curve in adults participating in a block resistance training program compared to a circuit resistance training program?
Ethics approval(s)

Approved 31/01/2025, Scientific Ethics Committee / Central University of Chile (Lord Cochrane 417, Torre A, Piso 6, Santiago, 8320000, Chile; +56 225826000; francisco.leon@ucentral.cl), ref: 02/2025

Health condition(s) or problem(s) studiedOverall fitness and recovery in healthy adults
InterventionCurrent interventions as of 16/04/2025:
The study involved a 12-week resistance training program with three weekly sessions (Monday, Wednesday, and Friday), each lasting 48 to 57 minutes. The participants were randomly assigned to either an experimental group (EG) or a control group (CG) using a stratified 1:1 allocation method to ensure unbiased group distribution.

The EG performed resistance exercises in blocks (Push-ups, Mountain climbers, Squats, Jumping Jacks, Burpees, and Skipping), while the CG performed the same exercises in a circuit format. The intensity was monitored using Polar® devices, and the training volume was the same for both groups, with differences only in the exercise distribution. The program was structured into warm-up (5 min), main phase (38-47 min), and cool-down (5 min). Heart rate was targeted at 60-90% of the maximum rate over the 12 weeks, with adjustments based on Karvonen’s formula. Both groups rested between repetitions and sets according to a fixed schedule, with total training time ranging from 38 to 47 minutes per session. Assessments were conducted before and after the program to evaluate physical activity levels, body composition, muscle strength, functional capacity, sprint performance, and recovery.




Previous interventions:
The study involved a 12-week resistance training program with three weekly sessions (Monday, Wednesday, and Friday), each lasting 43 to 52 minutes. The participants were randomly assigned to either an experimental group (EG) or a control group (CG) using a stratified 1:1 allocation method to ensure unbiased group distribution.

The EG performed resistance exercises in blocks (Push-ups, Mountain climbers, Squats, Jumping Jacks, Burpees, and Skipping), while the CG performed the same exercises in a circuit format. The intensity was monitored using Polar® devices, and the training volume was the same for both groups, with differences only in the exercise distribution. The program was structured into warm-up (5 min), main phase (38-47 min), and cool-down (5 min). Heart rate was targeted at 60-90% of the maximum rate over the 12 weeks, with adjustments based on Karvonen’s formula. Both groups rested between repetitions and sets according to a fixed schedule, with total training time ranging from 38 to 47 minutes per session. Assessments were conducted before and after the program to evaluate physical activity levels, body composition, muscle strength, functional capacity, sprint performance, and recovery.
Intervention typeBehavioural
Primary outcome measureBody composition is measured using the Metabolic Equivalent of Task, Body Mass Index and waist circumference at baseline and 12 weeks
Secondary outcome measuresCurrent secondary outcome measures as of 16/04/2025:
At baseline and 12 weeks:
1. Muscle strength measured using the right and left hand grip dynamometer
2. Speed assessed using a running anaerobic sprint test
3. Functional capacity measured using the 6-minute walking test
4. Recovery capacity using heart rate variability in the LF/HF ratio and RMSSD



Previous secondary outcome measures:
At baseline and 12 weeks:
1. Muscle strength measured using the right and left hand grip dynamometer
2. Speed assessed using a 35-meter sprint
3. Functional capacity measured using the 6-minute walking test
4. Recovery capacity using heart rate variability in the LF/HF ratio and RMSSD
Overall study start date30/01/2025
Completion date30/04/2025

Eligibility

Participant type(s)Healthy volunteer
Age groupAdult
Lower age limit18 Years
Upper age limit30 Years
SexBoth
Target number of participants30
Total final enrolment30
Key inclusion criteria1. Aged between 18 and 30 years and classified as a physically active adult.
2. Refrain from engaging in moderate or intense physical activity during the 48 hours prior to each session to prevent interference with acute training responses.
3. Attend all scheduled training sessions punctually throughout the 12-week intervention.
4. Read, understand, and sign the informed consent form before undergoing evaluations.
Key exclusion criteria1. Diagnosis of conditions such as hypertension, type 2 diabetes, coronary artery disease, or other cardiovascular or metabolic disorders.
2. Body mass index within the overweight or obese range, along with a waist circumference exceeding the high cardiometabolic risk threshold for the Chilean adult population.
3. Handgrip strength below the threshold for muscle weakness risk classification in the Chilean adult population.
4. Performance below the reference threshold for reduced functional capacity in the Chilean adult population.
5. Participation in another training program during the intervention, which could interfere with the study protocol response.
Date of first enrolment01/02/2025
Date of final enrolment02/02/2025

Locations

Countries of recruitment

  • Chile

Study participating centre

Pirque municipal stadium
G-405 14, Pirque, Metropolitan Region.
Santiago.
9480000
Chile

Sponsor information

Central University of Chile
University/education

Lord Cochrane 417, Torre A, Piso 6
Santiago
8320000
Chile

Phone +56 225826000
Email francisco.leon@ucentral.cl
Website https://www.ucentral.cl/investigacion-ucen/comite-etico-cientitico/contacto-comite

Funders

Funder type

Other

Investigator initiated and funded

No information available

Results and Publications

Intention to publish date30/04/2025
Individual participant data (IPD) Intention to shareYes
IPD sharing plan summaryAvailable on request
Publication and dissemination planPlanned publication in a peer-reviewed journal
IPD sharing planThe data sets generated and/or analyzed during the study will be available upon request to the authors.
hefuentes_@unap.cl

Study outputs

Output type Details Date created Date added Peer reviewed? Patient-facing?
Participant information sheet in Spanish 04/02/2025 No Yes

Additional files

46785 PIS.pdf
in Spanish

Editorial Notes

16/04/2025: The following changes were made:
1. The public title was changed from "Comparing the impact of two types of resistance exercises on body shape and fitness in adults".
2. The interventions and secondary outcome measures were updated.
3. The study contact email was updated throughout.
04/02/2025: Trial's existence confirmed by the Scientific Ethics Committee / Central University of Chile.