Cardiorespiratory Adaptations to High-Intensity Inter-val Training in Young Boxers
1 other identifier
interventional
16
1 country
1
Brief Summary
This study examined the effects of a structured 4-week high-intensity interval training (HIIT) program integrated with boxing on young trained individuals. Participants were randomly assigned to a HIIT-boxing group or a control group. Pre- and post-intervention assessments measured pulmonary function, aerobic capacity (VO₂max), and heart rate recovery (HRR) at 1, 3, and 5 minutes post-exercise. The study aimed to explore physiological adaptations, particularly improvements in cardiopulmonary and autonomic function. Integrating HIIT with boxing training may serve as an effective conditioning strategy for enhancing aerobic fitness, pulmonary function, and autonomic cardiovascular regulation in trained individuals. This combined approach could be valuable in sports performance programs and rehabilitation settings where improving VO₂max and recovery efficiency is a priority.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Feb 2024
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
February 25, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 25, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
July 25, 2024
CompletedFirst Submitted
Initial submission to the registry
June 5, 2025
CompletedFirst Posted
Study publicly available on registry
June 17, 2025
CompletedJune 17, 2025
June 1, 2025
4 months
June 5, 2025
June 12, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (5)
Forced Vital Capacity (FVC)
Pulmonary function tests were performed using a calibrated desktop spirometer (COSMED Pony FX; COSMED, Rome, Italy) to assess the key respiratory parameters. FVC was recorded to assess lung volume and respiratory strength. Participants performed a maximal inhalation followed by a forceful exhalation to expel as much air as possible. Unit of Measure: Liters (L)
baseline and after 4 weeks
Aerobic Capacity
Aerobic capacity was determined using the Yo-Yo Intermittent Recovery Level 1 (Yo-Yo IR1) test, a validated method for assessing maximal aerobic capacity in intermittent sports. The participants completed repeated 20-meter shuttle runs at increasing speeds, with short recovery periods between efforts. The aerobic capacity was predicted using the established regression equations for the Yo-Yo IR1 test.
baseline and after 4 weeks
Maximal Voluntary Ventilation (MVV)
MVV was measured using a calibrated desktop spirometer (COSMED Pony FX; COSMED, Rome, Italy) to evaluate overall ventilatory capacity. Participants were instructed to breathe in and out as rapidly and deeply as possible for 12-15 seconds; the value was extrapolated to represent the maximum volume of air inhaled and exhaled in one minute (L/min). Unit of Measure: Liters per minute (L/min)
Baseline and after 4 weeks
Forced Expiratory Volume in One Second (FEV1)
FEV1 was measured as the volume of air forcefully exhaled in the first second of the FVC maneuver. This value reflects airway patency and expiratory power. Unit of Measure: Liters (L)
Baseline and after 4 weeks
Peak Expiratory Flow (PEF)
PEF was assessed to determine the highest speed at which air can be expelled from the lungs during a forceful exhalation following full inspiration. Unit of Measure: Liters per minute (L/min)
Baseline and after 4 weeks
Study Arms (2)
Exercise group
EXPERIMENTALHIIT consisted of three weekly sessions, each including three blocks of five 30-second all-out punching intervals on a heavy bag, with 6-second rest between efforts and 1-minute rest between blocks.
control group
ACTIVE COMPARATORParticipants in both the experimental and control groups followed an identical boxing training program for a period of four weeks, with sessions conducted three times per week. Each session lasted 90 min and was structured in alignment with the established training principles for amateur boxing. The training began with a 15-minute general warm-up phase, including dynamic mobility drills and calisthenics, to elevate core temperature and enhance neuromuscular readiness.
Interventions
The experimental group completed a 4-week HIIT-boxing protocol, in addition to regular boxing sessions. HIIT consisted of three weekly sessions, each including three blocks of five 30-second all-out punching intervals on a heavy bag, with 6-second rest between efforts and 1-minute rest between blocks. Heart rate was monitored throughout, confirming training intensities of 88-92% HRmax, consistent with high-intensity training standards in combat sports.
Participants in control groups followed a boxing training program for a period of four weeks, with sessions conducted three times per week. Each session lasted 90 min and was structured in alignment with the established training principles for amateur boxing. The training began with a 15-minute general warm-up phase, including dynamic mobility drills and calisthenics, to elevate core temperature and enhance neuromuscular readiness.
Eligibility Criteria
You may qualify if:
- aged 18-30 years.
- Actively engaged in structured boxing training for at least 2 years.
- Training a minimum of 3 days per week.
- Free of cardiovascular, pulmonary, or neuromuscular conditions.
- Willing to abstain from non-study physical training 48 hours prior to testing.
- Provided written informed consent after receiving a full explanation of study procedures.
You may not qualify if:
- Had any diagnosed medical conditions contraindicating high-intensity exercise (e.g., uncontrolled asthma, cardiac arrhythmias).
- Reported current musculoskeletal injuries limiting full participation.
- Were taking medications affecting heart rate or respiratory function.
- Missed more than 10% of the assigned training sessions.
- Failed to adhere to pre-assessment instructions (e.g., rest or diet restrictions).
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Princess Nourah Bint Abdulrahman Universitylead
- Kocaeli Universitycollaborator
Study Sites (1)
Sena Cinarli
Kocaeli, Turkey (Türkiye)
Study Officials
- PRINCIPAL INVESTIGATOR
Cinarli
Department of Physiotherapy and Rehabilitation, Kocaeli Health and Technology University, Kocaeli,
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate prof
Study Record Dates
First Submitted
June 5, 2025
First Posted
June 17, 2025
Study Start
February 25, 2024
Primary Completion
June 25, 2024
Study Completion
July 25, 2024
Last Updated
June 17, 2025
Record last verified: 2025-06