Resistance Training, Detraining, and Retraining Study 2022
TraDeRe2022
Physiological Adaptations to Resistance Training, Detraining, and Retraining in Young Healthy Males and Females
1 other identifier
interventional
42
1 country
1
Brief Summary
The research project is aiming to examine the muscular adaptations to resistance training (RT), detraining (DT) and repeated RT (i.e. retraining). The research project will also examine differences in muscular adaptations between 20 weeks of continuous RT and 20 weeks of intermittent RT including a 10-week DT period in the middle of the training intervention. This is randomized controlled trial in which the research participants will be randomized into discontinuous and continuous groups (both n=\~20). Both will be doing a 2-3-week familiarization and control period at the start. Then in the former there will be an initial strength training period (10-wks), a DT period (10-wks), and a second strength training (retraining) period (10-wks). The second group includes a 10-wk non-training control period (10-wks) followed by a RT period (20-wks). Participants will be young, healthy men and women (age 18-35, which 50% are females) with no systematic RT experience during the last 6 months. Measurements will be completed before and after each study period. Body composition will be measured via bioelectrical impedance analysis (BIA) and 3D body scans. Dynamic leg press and elbow flexion one repetition-maximum (1RM) will be used to test maximal strength. Anaerobic performance and strength endurance will be tested in elbow flexion and dynamic leg press using RM tests. Vastus lateralis (VL) and biceps brachii muscle cross-sectional area (CSA) will be assessed via ultrasound. Muscle biopsies of the VL muscle will be obtained to assess changes in muscle fiber morphology and factors regulating and associated with the hypertrophic processes and metabolism. Blood samples will be collected to analyze changes in metabolism and physiology. A rating of perceived exertion (RPE) during training will be collected after every exercise to ensure proper training intensity. Finally, nutrition and habitual physical activity will be assessed with 4-day diet diaries and physical activity questionnaires before the intervention and during each 10-week period.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Mar 2022
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 1, 2022
CompletedFirst Submitted
Initial submission to the registry
March 2, 2022
CompletedFirst Posted
Study publicly available on registry
September 23, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2022
CompletedApril 10, 2024
April 1, 2024
10 months
March 2, 2022
April 8, 2024
Conditions
Outcome Measures
Primary Outcomes (1)
Change in upper and lower limb maximal strength after 10-week RT
Maximal muscle strength will be assessed via one repetition maximum (1RM) tests of both the leg press and barbell biceps curl exercises according to the NSCA's guidelines.
week -2, week 0, week 10
Secondary Outcomes (7)
Change in muscular performance after 20-week continuous RT period and two 10-week RT periods separated by a 10-week DT period
week -2, week 0, week 10, week 20, week 30
Change in upper and lower limb muscle CSA after 10-week RT period
week -2, week 0, week 10
Change in upper and lower limb muscle CSA after 20-week continuous RT period and two 10-week RT periods separated by a 10-week DT period
week 0, week 10, week 20, week 30
Changes in muscle fiber size during the intervention period
week 0, week 10, week 20, week 30
Change in lean mass during the intervention period
week -2, week 0, week 10, week 20, week 30
- +2 more secondary outcomes
Other Outcomes (3)
Changes in muscle fiber morphology and metabolism during the intervention period
week 0, week 10, week 20, week 30
Changes in metabolomics during the intervention period
week 0, week 10, week 20, week 30
Changes in proteomics during the intervention period
week 0, week 10, week 20, week 30
Study Arms (2)
10 week training, 10 week detraining, 10 week retraining
EXPERIMENTALParticipants (healthy untrained men and women, age 18-40) will conduct 10-week RT intervention and a 10-week DT period and the exact same 10-week RT intervention again. RT consists of two training sessions per week of total body workouts.
10 week non-training, 20 week continuous training
EXPERIMENTALParticipants (healthy untrained men and women, age 18-40) start with a 10-week non-training period and then continues with a 20-week RT intervention. RT consists of two training sessions per week of total body workouts.
Interventions
Participants (healthy untrained men and women, age 18-40) start with a 3-week familiarization and baseline measurement period. After that, they are randomized to two intervention groups, where other group will conduct 10-week RT intervention and a 10-week DT period and again the exact same 10-week RT intervention again whereas the other group start with a 10-week non-training period and then continues with a 20-week RT intervention. RT consists of two training sessions per week of total body workouts. Same measurements are conducted for both groups with the same time intervals.
Eligibility Criteria
You may qualify if:
- No regular resistance training history
- BMI within range 18.5-30 kg/m2
- Participants must be 18-40 years old
- No history in systematic endurance-type training (\> 2 endurance exercise sessions lasting \> 30 minutes per week for the last six months)
- non-smoker
- not currently consuming any anti-inflammatory drug(s)
You may not qualify if:
- history of medication that could affect exercise responses
- use of nutritional supplements aside from those that are protein- or carbohydrate-based (ex. creatine) or basic minerals, vitamins, or fish oil products
- any acute or chronic illness affecting cardiovascular, respiratory, musculoskeletal and/or endocrine function
- any other condition that may limit the ability to perform resistance training and testing (ex. uncontrolled hypertension, diabetes, arthritic conditions, neuromuscular complications)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Jyväkylä
Jyväskylä, Central Finland, 40014, Finland
Related Publications (1)
Halonen EJ, Gabriel I, Kelahaara MM, Ahtiainen JP, Hulmi JJ. Does Taking a Break Matter-Adaptations in Muscle Strength and Size Between Continuous and Periodic Resistance Training. Scand J Med Sci Sports. 2024 Oct;34(10):e14739. doi: 10.1111/sms.14739.
PMID: 39364857DERIVED
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- BASIC SCIENCE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 2, 2022
First Posted
September 23, 2022
Study Start
March 1, 2022
Primary Completion
December 31, 2022
Study Completion
December 31, 2022
Last Updated
April 10, 2024
Record last verified: 2024-04
Data Sharing
- IPD Sharing
- Will not share