"CORE Training for Musculoskeletal Health: A Study on Adaptive Exercise Protocols"
RCT-EMG-US-QoL
Development and Implementation of a Core Training Protocol: Effects on Muscle Activation, Hypertrophy, Balance, and Quality of Life in Recreationally Active Adults
1 other identifier
interventional
40
1 country
1
Brief Summary
This study aims to evaluate the effects of an adaptive core training protocol that integrates core stability, core strength, and high-intensity core power exercises on muscle activation, hypertrophy, balance, and quality of life. Forty recreationally active adults with a minimum of two years of consistent training experience will participate. The structured intervention will span multiple weeks and utilize electromyography (EMG), ultrasound imaging, and validated questionnaires to assess neuromuscular and functional adaptations.
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 Oct 2025
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
First Submitted
Initial submission to the registry
June 10, 2025
CompletedFirst Posted
Study publicly available on registry
June 17, 2025
CompletedStudy Start
First participant enrolled
October 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 28, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
March 15, 2026
CompletedJune 25, 2025
June 1, 2025
5 months
June 10, 2025
June 19, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Electromyographic (EMG) Muscle Activation During Medicine Ball Overhead Slam
Surface EMG recordings will assess neuromuscular activation in the rectus abdominis (RA), external oblique (EO), and iliocostalis lumborum (IL) muscles. Measurements will be conducted pre- and post-intervention using Biopac Systems Inc. electrodes and TEL100 M transmitter, with signals filtered between 10-500 Hz. Data will be analyzed via Acknowledge software to determine training-induced improvements in core muscle activity patterns.
Baseline (Week 0) and Post-Intervention (Week 8)
Secondary Outcomes (3)
Ultrasound-Based Core Muscle Hypertrophy Assessment
Baseline (Week 0) and Post-Intervention (Week 8)
Balance & Postural Stability Evaluation (Force Plate Analysis)
Baseline (Week 0) and Post-Intervention (Week 8)
Psychometric Evaluation of Life Satisfaction (Satisfaction With Life Scale - SWLS)
Baseline (Week 0) and Post-Intervention (Week 8)
Other Outcomes (2)
Kinematic Angular Velocity Analysis (Motion Capture)
Baseline (Week 0) and Post-Intervention (Week 8)
Psychometric Evaluation of Life Satisfaction (SWLS)
Baseline (Week 0) and Post-Intervention (Week 8)
Study Arms (2)
Experimental Group - Progressive Core Training Protocol
EXPERIMENTALParticipants in this arm will follow an eight-week structured core training protocol designed to enhance neuromuscular adaptations, core muscle hypertrophy, and biomechanical performance. The program incorporates progressive core stability, core strength, and high-intensity core power exercises, ensuring gradual intensity scaling and optimized movement efficiency. Training sessions include warm-up, eight structured triads of core exercises, and a cool-down phase. Assessments will track electromyographic activity, ultrasound muscle imaging, balance performance, and kinetic chain optimization.
Control Group - Standardized Core Routine
ACTIVE COMPARATORParticipants in this arm will engage in a standardized core exercise routine performed twice per week. The intervention will not include progressive intensity or specialized neuromuscular activation techniques. Control group participants will perform basic abs and back exercises to maintain general core function without targeted adaptations. The purpose of this arm is to serve as a baseline comparison for neuromuscular, biomechanical, and psychological assessments between groups.
Interventions
This structured training intervention incorporates progressive core exercises designed to enhance neuromuscular activation, balance, and muscle hypertrophy. Participants perform eight exercise triads per session, progressing from core stability drills to high-intensity power movements over eight weeks.
Control group participants engage in general core activation exercises twice per week, without progressive intensity or specialized neuromuscular adaptation.
Eligibility Criteria
You may qualify if:
- Aged 25-35 years
- Physically active (≥3 sessions/week, ≥1 hour per session) for ≥2 years
- No known musculoskeletal, cardiovascular, or neurological disorders
- No engagement in structured core training programs
- Available to attend all evaluation appointments
- Able and willing to commit to the 8-week intervention program
You may not qualify if:
- Medical conditions that limit full-body or trunk movement
- Cardiovascular/metabolic conditions contraindicating high-intensity exercise
- Current participation in Pilates, CrossFit, or other core-specific protocols
- Recent musculoskeletal injury affecting training eligibility
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Aristotle University of Thessaloniki, Serres Campus - Neuromechanics Laboratory
Serres, Central Makedonia, 62100, Greece
Related Links
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Ioannis Tsartsapakis, Ph.D.
Aristotle University of Thessaloniki, Greece
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- BASIC SCIENCE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Laboratory Teaching Staff - Laboratory of Neuromechanics. Department of Physical Education and Sport Science at Serres, Aristotle University of Thessaloniki
Study Record Dates
First Submitted
June 10, 2025
First Posted
June 17, 2025
Study Start
October 1, 2025
Primary Completion
February 28, 2026
Study Completion
March 15, 2026
Last Updated
June 25, 2025
Record last verified: 2025-06