Virtual Training Based on Supersets vs. Concurrent Training in Women.

July 19, 2022 updated by: Victor Hugo Arboleda Serna, Universidad de Antioquia

The Effects of Eight Weeks of Virtual Training Based on Supersets vs. Concurrent Training on Muscle Strength, Cardiorespiratory Fitness, Motivation, Adherence, and HRQL in Women With Low to Moderate Levels of Physical Activity.

There are different forms of physical activity proven to improve muscular strength and cardiorespiratory fitness. One of them is concurrent training, which is defined as the combination of two or more physical capacities in the same session (resistance and endurance training). Another modality is superset training, which is characterized by performing two or more exercises for the same muscle group, or a different muscle group, consecutively, with minimal recovery between them.

To date, the evidence has shown studies comparing different resistance training protocols, vs. aerobic training, and vs. concurrent training, performed in various ways, on muscle strength and cardiorespiratory fitness. Most of these studies involved men with resistance training experience, and little research linked women. It should be noted that no study found has used virtual training to test the effects of superset training compared to concurrent training in women with low to moderate levels of physical activity.

Therefore, this study aims to identify the effect of a superset training program vs. a concurrent training program on muscle strength, cardiorespiratory fitness, motivation, adherence, and health-related quality of life in women with a low to moderate level of physical activity for eight weeks virtually.

Study Overview

Status

Completed

Conditions

Detailed Description

Sixty women will be randomly assigned to two groups (superset and concurrent). The interventions will be carried out virtually asynchronously, only sessions 1, 5, 9, 13, 17, and 21 will be supervised synchronously. Follow-up will be done through WhatsApp messages. Both groups will have a training frequency of 3 times a week for eight weeks. In the training sessions, strength exercises with self-loading (crunches, one leg squat, side plank, push up, deadlift, lumbar extension stretch, row, glute bridge, front raise) and/or aerobic exercises (floor tape squat, jumping jacks, skaters). Each group will execute the same number of series and repetitions during the 8 weeks, the performance of strength exercises will be standardized at 45 bpm throughout the protocol, and aerobic exercises at 70 bpm. Intensity will be controlled by resting between sets, starting with 90 seconds in week one, decreasing by 15 seconds every two weeks until reaching 45 seconds.

Each participant will have initial and final evaluations to measure muscle strength in lower, middle, and upper kinetic chains. Queen's College test will be used to assess cardiorespiratory fitness, BREQ-2, and SF-12 questionnaires will be used to measure motivation and health-related quality of life respectively.

Study Type

Interventional

Enrollment (Actual)

60

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

    • Antioquia
      • Medellín, Antioquia, Colombia
        • Universidad de Antioquia

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 40 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Female

Description

Inclusion Criteria:

  • Healthy women
  • Physical activity (<600 to ≤1500 MET/min/wk)

Exclusion Criteria:

  • Diabetes
  • Hypertension
  • History of cardiovascular disease
  • History of coronary heart disease
  • Osteoporosis
  • Pregnancy
  • Breast-feeding women
  • Psychological, neuromotor, and/or osteo-muscular conditions that may affect participation in an exercise program.

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: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Superset
This group will perform three strength circuit training. Each circuit training consists of three exercises (lower, middle, and upper body exercises) performed in a supersets fashion. This order makes it less complex, which is important given the characteristics of the population.

A strength circuit training will be performed in a supersets fashion. Three strength circuit training in three blocks.

  1. One leg squat, side plank, and push up.
  2. Deadlift, lumbar extension stretch, and row.
  3. Glute bridge, crunches, and front raise.
Active Comparator: Concurrent
This group will perform six resistance exercises in a traditional fashion (three exercises for the lower body, three exercises for the upper body) and three aerobic exercises (floor tap squat, jumping jacks, and skaters).
Six resistance exercises in a traditional fashion: three exercises for the lower body (one leg squat, deadlift, and glute bridge). Three exercises for the upper body (push up, row, and front raise). And three aerobic exercises (floor tap squat, jumping jacks, and skaters).

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in muscular strength
Time Frame: Baseline and 8-weeks
Test: One leg squat, leg lever, and push up. A maximum number of repetitions as possible to failure.
Baseline and 8-weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Cardiorespiratory fitness
Time Frame: Baseline and 8-weeks

Queens College Step Test

The test consists of 3 minutes of stepping up and down on a 41.3 cm step at a set rate of 22 steps per minute for females and at 24 steps per minute for males. Estimation of VO2max can be calculated from the test results as follow:

Men: VO2max(ml/kg/min) = 111.33 - (0.42 x heart rate (bpm) Women: VO2max(ml/kg/min) = 65.81 - (0.1847 x heart rate (bpm)

Baseline and 8-weeks
Health-related quality of life
Time Frame: Baseline and 8-weeks
Short Form 12 Health Survey (SF-12) Short Form 12 Health Survey (SF-12) Physical component score (PCS) 0-100 Mental component score (MCS) 0-100 The scores have a mean of 50 with a standard deviation of 10. Values above or below 50 indicate a better or worse state of physical or mental health.
Baseline and 8-weeks
Motivation to exercise
Time Frame: Baseline and 8-weeks
Behavioural Regulation in Exercise Questionnaire-2 (BREQ-2). BREQ-2 has a Likert-type scale of 5 points, where 0 = not true for me and 4 = very true for me.
Baseline and 8-weeks
Exercise adherence
Time Frame: Baseline and 8-weeks
Attendance at exercise sessions
Baseline and 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)

January 12, 2022

Primary Completion (Actual)

April 26, 2022

Study Completion (Actual)

June 30, 2022

Study Registration Dates

First Submitted

April 26, 2022

First Submitted That Met QC Criteria

April 26, 2022

First Posted (Actual)

May 2, 2022

Study Record Updates

Last Update Posted (Actual)

July 21, 2022

Last Update Submitted That Met QC Criteria

July 19, 2022

Last Verified

July 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • Virtual Superset-UdeA

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.

Clinical Trials on Healthy Volunteers

Clinical Trials on Superset

Subscribe