Superset Strength Training for Time-efficiency

Superset Strength Training for Time-efficiency - A Randomized Controlled Pilot Study

Physical inactivity is a global challenge and there is an urgent need to find strategies to increases people's activity levels. Strength training is one of the activities that is recommended to engage in regularly by both the American College of Sports Medicine and the World Health Organization. Understanding how strength training can be done effectively without spending much time could potentially increase people's involvement in strength training, as lack of time often is reported as barrier to training. Superset strength training can potentially be a time-efficient way of strength training, as this training method has been found to take half the time of the traditional ways of training.

The aim of the present study is therefore to compare the effects of superset strength training and traditional strength training on muscular strength, body composition and fatigue.

Study Overview

Study Type

Interventional

Enrollment (Actual)

30

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

      • Trondheim, Norway, 7491
        • Norwegian University of Science and Technology

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

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • living in Trøndelag
  • did not perform weekly strength training during the past 6 months.

Exclusion Criteria:

  • any known severe somatic condition (e.g., autoimmune and systemic inflammatory diseases, cancer, severe osteoporosis)
  • any known severe psychiatric condition
  • other contraindications for heavy resistance training (e.g. shoulder pain).

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: Superset strength training
This is the experimental group that performs strength training with sets and rest intervals programmed in a superset manner
Three weeks of familiarization (two times per week) to the exercises leg-press, bench press, lateral pulldown and seated rows, followed by superset strength training two days per week for 12-weeks. Superset 1 are bench-press and seated rows, and superset 2 are leg-press and lateral pulldown. Each superset is performed three times.
Active Comparator: Traditional strength training
This is the comparator group that engages in strength training with sets and rest intervals programmed in accordance with the recommendations from The American College of Sports Medicine
Three weeks of familiarization (two times per week) to the exercises leg-press, bench press, lateral pulldown and seated rows, followed by strength training two days per week for 12-weeks. Each exercise is performed for three sets with rest intervals between each set.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in muscular strength
Time Frame: 3 months
Change in one repetition maximum strength (weight in kilograms) for all exercises
3 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in body weight
Time Frame: 3 months
Assessed using a body composition analyzer (i.e. InBody)
3 months
Change in muscle mass
Time Frame: 3 months
Assessed using a body composition analyzer (i.e. InBody)
3 months
Change in body composition fat mass
Time Frame: 3 months
Assessed using a body composition analyzer (i.e. InBody)
3 months
Change in body composition BMI
Time Frame: 3 months
Assessed using a body composition analyzer (i.e. InBody)
3 months

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Training load
Time Frame: continuously for 3 months
Assessed by training diaries
continuously for 3 months
Training volume
Time Frame: continuously for 3 months
Assessed by training diaries
continuously for 3 months
Perceived exhaustion
Time Frame: continuously for 3 months
Borg Category Ratio Scale (0-10) - information from training diaries
continuously for 3 months
Participant's experiences with the intervention
Time Frame: 3 months
Semi-structured focus group interviews with questions regarding the experience participant had during the intervention, questions related to the training program, questions related to motivation and fatigue, questions related to time-efficiency
3 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Vegard moe Iversen, PhD, Norwegian University of Science and Technology

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)

August 5, 2019

Primary Completion (Actual)

December 20, 2019

Study Completion (Actual)

December 20, 2019

Study Registration Dates

First Submitted

July 18, 2019

First Submitted That Met QC Criteria

July 29, 2019

First Posted (Actual)

July 30, 2019

Study Record Updates

Last Update Posted (Actual)

July 7, 2020

Last Update Submitted That Met QC Criteria

July 3, 2020

Last Verified

July 1, 2020

More Information

Terms related to this study

Other Study ID Numbers

  • 2019-07-VMI

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.

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