Resistance Training, Detraining, and Retraining Study 2024 (TraDeRe2024)
NCT06573086 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 90
Last updated 2025-04-06
Summary
The goals of our research project are to identify factors explaining inter-individual variation in responses to resistance training (RT) and the baseline determinants underlying an individual's sensitivity to respond to RT. Moreover, investigators aim to assess whether a responsiveness to RT predicts responsiveness to endurance training (ET). Thus, investigators aim to gain a deeper understanding of exercise adaptation processes. The main questions investigators aim to answer are:
* Can the physiological responses of one RT intervention be extrapolated to a subsequent RT intervention?
* If so, what are the mechanisms underlying differing skeletal muscle growth responses in low, and high responders of skeletal muscle hypertrophy?
* If so, do the low responders of skeletal muscle growth respond more favourably when the amount of RT is increased?
* Are the high, moderate, and low responders of RT also the highest, moderate, and lowest responders to ET?
To examine these main research questions, high (n=30), low (n=30), and moderate (n=30) responders of skeletal muscle growth in response to RT (intervention I, NCT05874986) are reallocated into a subsequent 12-week RT intervention (intervention II) after a detraining period. A subgroup of these participants (n=10) will engage in a 6-week control period before starting the second RT period. Additionally, after intervention II, participants will participate in an ET intervention, lasting 6 weeks.
In this intervention II, reallocated participants will be:
* Resistance training with supervision for 12 weeks
* Consuming deuterium oxide for the assessment of muscle protein synthesis
* Consuming D3-3-methylhistidine for the assessment of acute muscle protein breakdown
* Consuming D3-creatine for the examination of whole-body skeletal muscle mass
* Providing a spot urine sample six (6) times, and urine collection for 24 hours performed twice
* Providing saliva samples (30-32 in total) for the assessment of body water enrichment of deuterium
* Providing a muscle biopsy four or five (4-5) times during the study
* Providing a blood sample fourteen (14) times during the study
* Assessed for body composition and body volume four or five times (4-5) during the study
* Participating in muscle size, maximal dynamic strength and TMS measurements four or five (4-5) times during the study
* Asked to answer questionnaires related to e.g. stress, physical activity, sleep, perceived exertion, and diet
* Participating in recovery measurements before and after the second-to-last and the last RT bout, and once in the days between these RT bouts, consisting of six (6) body volume measurements and six (6) maximal voluntary isometric contraction (kg) tests using horizontal leg press for the assessment of neuromuscular recovery
* Participating in an acute resistance exercise (RE) after the 12-week RT intervention.
Furthermore, in the ET intervention, participants will be:
* Participating in a familiarization session and resting electrocardiograph measurements before the intervention
* Participating in endurance testing consisting of body composition, movement economy, and incremental RAMP testing before and after ET intervention
* Endurance training with supervision for 6 weeks, three times a week.
Conditions
- Hypertrophy
- Exercise Training
- Skeletal Muscle Atrophy
- Healthy
Interventions
- OTHER
-
Resistance Training
12-week resistance training
Sponsors & Collaborators
-
Academy of Finland
collaborator OTHER -
University of Jyvaskyla
lead OTHER
Principal Investigators
-
Juha P Ahtiainen, Assoc.Prof. · University of Jyväskylä, Faculty of Sport and Health Sciences
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- BASIC_SCIENCE
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 50 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2024-08-19
- Primary Completion
- 2025-06-15
- Completion
- 2025-06-15
Countries
- Finland
Study Locations
More Related Trials
-
Exercise Training Adherence After Cardiac Rehabilitation in Coronary Heart Disease Patients
NCT01246570 ·Status: COMPLETED ·Phase: NA
-
Evaluation of the Effects of Eccentric Muscle Training Versus Conventional Concentric Training in Chronic Heart Failure
NCT02046707 ·Status: COMPLETED ·Phase: NA
-
Tailored Versus Traditional Resistance Exercise
NCT06449716 ·Status: COMPLETED ·Phase: NA
-
Exercise in Hereditary ATTR (ATTRv) Amyloidosis
NCT07033715 ·Status: RECRUITING ·Phase: NA
-
High-intensity Exercise After Acute Cardiac Event (HITCARE)
NCT02235753 ·Status: TERMINATED ·Phase: NA
-
Keeping Active in Residential Elderly
NCT03141879 ·Status: UNKNOWN ·Phase: NA
-
The Utility of Focused Frailty Interventions on Patients With Advanced Heart Failure
NCT03574662 ·Status: COMPLETED ·Phase: NA
-
Implementation and Evaluation of Real Time Monitoring of Physical Activity in Geriatric Patients - a Hybrid Implementation and Effectiveness Study in Two Patient Cohorts
NCT06421246 ·Status: COMPLETED
-
Effects of Personalized Physical Rehabilitation in Kidney Transplant Recipients
NCT02409901 ·Status: COMPLETED ·Phase: NA
-
The Effects of Combined Exercise Training on Exercise Capacity in Cardiac Rehabilitation
NCT01921036 ·Status: COMPLETED ·Phase: NA
-
Training Intervention in Heart Failure and Frail Elderly Population
NCT02365155 ·Status: UNKNOWN ·Phase: NA
-
Effectiveness of Combined Aerobic and Strength Training in Acute and Chronic Adaptations in Patients With Heart Failure
NCT03320655 ·Status: COMPLETED ·Phase: NA
-
Exercise Therapy to Reduce Heart Failure Symptoms; Sorting Mechanisms of Benefit
NCT03648762 ·Status: COMPLETED ·Phase: NA
-
Exercise Training in Transthyretin Cardiac Amyloidosis
NCT05797857 ·Status: RECRUITING ·Phase: NA
-
Different Endurance Training Protocols in Cardiac Rehabilitation
NCT01493193 ·Status: COMPLETED ·Phase: PHASE4
-
Does Cardiorespiratory Interval Training Improve Post-stroke Fatigue
NCT03458884 ·Status: RECRUITING ·Phase: NA
-
Preventing Hospital Associated Disability in Older Patients: Individualized Nutrition and Exercise Strategy, a Feasibility Study
NCT07124338 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
Electronic Cardiac Rehabilitation (eCardiacRehab) Feasibility Study
NCT06759805 ·Status: RECRUITING ·Phase: NA
-
A Twice-Daily Individual Targeted Exercise Program in Frail Hospitalised Older Medical In-patients (RCT)
NCT02463864 ·Status: COMPLETED ·Phase: NA
-
Effect of Intradialytic Exercise In The United Arab Emirates
NCT03131804 ·Status: COMPLETED ·Phase: NA
-
Exercise Intervention in Patients With Heart Failure With Preserved and Reduced Ejection Fraction
NCT05255172 ·Status: ENROLLING_BY_INVITATION ·Phase: NA
-
Different Endurance Training Protocols in Cardiac Patients
NCT02303379 ·Status: COMPLETED ·Phase: NA
-
Physical Training and Health Education in Hospitalized Elderly
NCT03604640 ·Status: COMPLETED ·Phase: NA
-
Elaboration and Analysis of a New Cardiac Risk Stratification Protocol Based on Clinical and Physical Variables
NCT04790643 ·Status: COMPLETED
-
Resistance Training in Cardiovascular Disease Patients
NCT04638764 ·Status: UNKNOWN ·Phase: NA