Clinical trial

Effect of Low Volume Sprint Interval Training on Cardiorespiratory Fitness

Recruiting now · Not applicable · 1 countries · Registry ID NCT07328568

Recruiting nowNot applicableInterventional

What this study is about

Low levels of physical activity (PA) are related to poor health and greater risk of premature death in adults. Lack of time is cited as a primary barrier to partaking in PA. In the last 20 years, a lot of attention has been directed towards the efficacy of high intensity interval training (HIIT), which consists of brief, intense bursts of PA separated by recovery. One primary benefit of HIIT is a sizable increase in cardiorespiratory fitness (CRF), which enables adults to exercise better and reduce health risks due to the strong link between health status and CRF. Completion of cardiovascular exercise is typically recommended for all adults to increase CRF, yet it takes a lot of time and may be perceived as boring. Alternatively, HIIT requires less time and tends to cause greater feelings of enjoyment in many adults. Hundreds of studies report an increase in CRF in response to HIIT in various groups of adults ranging from athletes and those with obesity, diabetes, cancer, stroke, and even spinal cord injury, which emphasizes the potency of this vigorous form of PA. Yet, many studies are weakened by a small sample size which questions the feasibility of these findings. This randomized controlled trial will test the efficacy and feasibility of a very small amount of HIIT, referred to as reduced exertion high intensity interval training (REHIT), in inactive adults. In the proposed study, REHIT will consist of 2 days per week of 1 to two 10 - 20 second sprints on a stationary bike. The proposed sample will include 60 adults who complete 18 sessions of REHIT over a 9 week period, and their responses will be compared to a non exercising control group. During the study, changes in CRF, fuel metabolism, and psychological responses will be monitored, with the latter outcome shedding light on the overall feasibility of HIIT in inactive adults. Overall, this novel study has profound public health applications as it will assess fitness and health related changes to a small dose of PA in the largest sample to date. If substantial changes in CRF are shown, these data have the potential to modify public health guidelines for implementing PA in inactive adults.

A promising-looking record is not the same as confirmed eligibility. The study team must review the full criteria and current recruitment status.

Basic eligibility

Age18 Years to 55 Years
SexAll
Healthy volunteersNot accepted
ConditionInactivity, Physical, Overweight (BMI > 25), Healthy Participants

Full registry criteria

Inclusion Criteria: * Healthy * BMI \< 35 kg/m2 * younger than 56 yr old * no joint issues Exclusion Criteria: * Those adults who are currently active and not weight stable * Adults with BMI \> 35 kg/m2 * Use of medications which may alter study outcomes

Treatments and study arms

High intensity interval training

Other

Participants will complete 24 sessions of REHIT and their responses will be compared to a non exercising control group.

Primary outcomes

Cardiorespiratory fitnessCRF will be assessed at baseline 48 - 72 hours before the start of training, and at 6 and 12 weeks of training, which represent halfway and end of training. The assessments will be performed at least 24 hours after sessions of exercise training.

Cardiorespiratory fitness (CRF) is determined by oxygen transport from cardiovascular system to mitochondria and is strongly related to health status and premature mortality. It will be assessed using VO2max testing on a cycle ergometer and expressed in mL/kg/min.

Study locations

1 locations were listed when this page was built. The first 40 are shown.

California State University--San Marcos Human Performance Laboratory🇺🇸 San Marcos, California, United States
Todd A Astorino, Ph.DContact
Todd Anthony Astorino, Ph.DPrincipal Investigator