- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04038177
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
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Trondheim, Norway, 7491
- Norwegian University of Science and Technology
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
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
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
Investigators
- Principal Investigator: Vegard moe Iversen, PhD, Norwegian University of Science and Technology
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2019-07-VMI
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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