- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06449300
Effects of Different Volumes of Resistance Training
Effects of Different Volumes of Resistance Training on Body Composition, Peak Power, and Muscle Thickness in Untrained Healthy Women
This study explores the effects of varying volumes of resistance training on body composition, strength, peak power, and muscle thickness in untrained women over eight weeks. A randomized controlled trial involving 45 female college students assessed the outcomes across three groups: low-volume training (LVT) with three weekly sessions, moderate-volume training (MVT) with four weekly sessions, and high-volume training (HVT) with five weekly sessions. Participants were untrained, aged 18-65, and free from cardiovascular diseases or performance-enhancing drugs.
The hypothesis suggested that moderate volume training would yield optimal muscle development, considering the potential non-linear dose-response relationship where excessive training might be detrimental. Measurements included body composition, muscle thickness, and peak power through a force platform during vertical jumps.
Data analysis focused on changes in muscle thickness, strength, and body composition, with statistical significance set at p < 0.05. The study aimed to provide insights into how different training volumes affect physiological adaptations in untrained women, potentially guiding fitness regimen optimizations for similar populations.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The study aimed to investigate the effect of different resistance training volume (low-, moderate, and high) on body composition, maximal strength, peak power, and muscle thickness in untrained women over eight weeks. The study is a three-arm, randomized controlled trial, 45 female college students participated, fit the specific inclusion criteria like age between 18-65 and being untrained. Exclusion criteria included the use of performance-enhancing drugs or recent resistance training.
Participants were randomly assigned to one of three groups: low-volume training (LVT) with three sessions weekly, moderate-volume training (MVT) with four sessions weekly, and high-volume training (HVT) with five sessions weekly. Each session comprised 12 exercises. Split split-strength training method was applied. After participants' 1RM maximums were determined, training loads were calculated separately for each participant. All workouts were conducted by certified trainers to ensure they were performed in the correct training format. Each training session lasted approximately 60 minutes. The weekly training loads of all participants were increased by 5%. In the LVT group, 3 sets of 8-12 repetitions of: between sets interval: 120 seconds (3 days/wk), in the MVT group, 3 sets of 8-12 repetitions of: between sets interval: 120 seconds (4 days/wk), in the HVT group, 3 sets of 8-12 repetitions of: between sets interval: 120 seconds exercises (5 days/wk) were performed.
Results and data analysis involved anthropometric measurements, muscle thickness via ultrasound, and peak power from the vertical jump test. Statistical significance was set at p < 0.05, and effect sizes were calculated with Partial Eta Squared values.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Riyadh, Saudi Arabia, 11671
- Princess Nourah Bint Abdulrahman University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Adult women between ages of 18 -65 years old
- Able to walk independently
- Free of any history of cardiovascular disease
- Untrained (less than 150 min of PA/week)
Exclusion Criteria:
- Intake of performance-enhancing drugs, anabolic steroids
- Any history of injury, or physiological or physical limitations that could affect the ability to perform training and physical testing in the last year.
- Those who had been RT for more than 2 months in the previous 6 months were excluded.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: low volume (LVT) resistance training
3 sessions of 12 exercises per week for 8 weeks .
Split-strength training method will be applied.
After participants' 1RM maximums were determined, training loads were calculated separately for each participant.
All workouts will be conducted by certified trainers to ensure they are performed in the correct training format.
Each training session lasted approximately 60 minutes.
The weekly training loads of all participants will be increased by 5%.
In the MVT group, 3 sets of 8-12 repetitions: between sets intervals: of 120 seconds will be performed.
|
(low volume training - 3 sessions of 12 exercises per week)
|
|
Active Comparator: moderate volume (MVT) resistance training
4 sessions of 12 exercises per week for 8 weeks .
Split-strength training method will be applied.
After participants' 1RM maximums were determined, training loads were calculated separately for each participant.
All workouts will be conducted by certified trainers to ensure they are performed in the correct training format.
Each training session lasted approximately 60 minutes.
The weekly training loads of all participants will be increased by 5%.
In the MVT group, 3 sets of 8-12 repetitions: between sets intervals: of 120 seconds will be performed.
|
(moderate volume training - 4 sessions of 12 exercises per week)
|
|
Active Comparator: high volume (HVT) resistance training
5 sessions of 12 exercises per week for 8 weeks .
Split-strength training method will be applied.
After participants' 1RM maximums were determined, training loads were calculated separately for each participant.
All workouts will be conducted by certified trainers to ensure they are performed in the correct training format.
Each training session lasted approximately 60 minutes.
The weekly training loads of all participants will be increased by 5%.
In the MVT group, 3 sets of 8-12 repetitions: between sets intervals: of 120 seconds will be performed.
|
(high volume training - 5 sessions of 12 exercises per week)
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Anthropometric measurements
Time Frame: at baseline and end of 8 week
|
Bio-impedance body composition analysis system
|
at baseline and end of 8 week
|
|
Muscle thickness measurements
Time Frame: at baseline and end of 8 week
|
A portable ultrasound scanner will be used to determine muscle thickness.
At one location, muscle thickness will be measured: Between the greater trochanter and the lateral epicondyle of the thigh, the thickness of the quadriceps femoris (Vastus lateralis) will be measured at 50%.
Ultrasound tests will be done at the start of the study and 8 weeks later, by a researcher blinded to the interventions.
All tests were performed in the morning when participants are fasting.
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at baseline and end of 8 week
|
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Countermovement Jump (CMJ)
Time Frame: at baseline and end of 8 week
|
Countermovement Jump (CMJ) values of all participants will be measured.
Peak muscle power measures in watts (W) using the Accupeak power2.0
portable force platform system .
The measurement frequency of the device was set to 500 Hz.
Participants will undrergo a 10-minute warm-up program before completing a CMJ.
Participants will be asked to begin a downward movement and jump as high as possible after hearing a tone from the computer.
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at baseline and end of 8 week
|
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Body height measurements
Time Frame: at baseline and end of 8 week
|
A stadiometer is attached to the wall.
It has a sliding horizontal headpiece that's adjusted to rest on top of your head.
The measurement of height will be conducted using a Mesilife portable stadiometer.
|
at baseline and end of 8 week
|
Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Dondu Ugurlu, Phd, dondusimsek@kku.edu.tr
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
- 2021.11.07
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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