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Sprint Interval Training in Young Sedentary Adults

Effects of Sprint Interval Training on Cardiovascular Capacity and VO2max in Young Sedentary Adults: A Randomized Controlled Trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07596836
Acronym
SIT
Enrollment
40
Registered
2026-05-19
Start date
2026-03-11
Completion date
2026-04-22
Last updated
2026-05-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiorespiratory Fitness, Sedentary Lifestyle

Keywords

Sprint interval training, VO2max, Cardiorespiratory fitness, Resting heart ratev, 6-minute walk test, Sedentary adults, Young adults, Randomized controlled trial

Brief summary

This randomized controlled trial evaluated the effects of a 6-week supervised sprint interval training program on cardiorespiratory fitness in healthy sedentary young adults. Forty participants aged 20 to 25 years were randomly assigned to either a sprint interval training group or a control group. The sprint interval training group completed supervised cycle-ergometer sessions three times per week for 6 weeks, while the control group maintained their usual sedentary routine. The primary outcome was maximal oxygen uptake (VO2max). Secondary outcomes included resting heart rate and 6-minute walk test distance. The study aimed to determine whether a short-term, time-efficient sprint interval training program could improve cardiovascular capacity and functional exercise performance in sedentary young adults.

Detailed description

This study was designed as a randomized controlled pre-test and post-test intervention study. Healthy sedentary adults aged 20 to 25 years were enrolled after ethics approval and written informed consent. Participants were randomly allocated in a 1:1 ratio to either a supervised sprint interval training group or a control group. The sprint interval training group performed supervised exercise sessions on a cycle ergometer three times per week for 6 weeks. Each session included a 5-minute warm-up, followed by repeated 30-second all-out sprint bouts with active recovery periods. The number of sprint repetitions was progressively increased during the intervention period. The control group maintained their usual sedentary lifestyle and did not receive an additional exercise program. Outcome measurements were performed before and after the intervention. The primary outcome was VO2max, assessed using a maximal exercise test on a cycle ergometer with respiratory gas analysis. Secondary outcomes were resting heart rate and 6-minute walk test distance. Adherence and adverse events were monitored throughout the study period.

Interventions

The sprint interval training intervention consisted of supervised cycle-ergometer sessions performed three times per week for 6 weeks. Each session included a 5-minute warm-up at 50% VO2max, followed by 4 to 6 repetitions of 30-second all-out sprint bouts on a Monark 894E cycle ergometer, with 4-minute active recovery periods between sprints. The number of sprint repetitions was progressively increased from 4 repetitions in the first two weeks to 6 repetitions in the following four weeks.

Sponsors

Sezer Taştan
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Masking description

No masking was used because participants and research staff were aware of the exercise-training intervention.

Intervention model description

Participants were randomly assigned in a 1:1 ratio to either a supervised sprint interval training group or a control group.

Eligibility

Sex/Gender
ALL
Age
20 Years to 25 Years
Healthy volunteers
Yes

Inclusion criteria

* Aged 20-25 years * Healthy sedentary adult * Engaging in less than 150 minutes/week of moderate-to-vigorous physical activity * IPAQ score below 600 MET-min/week or not participating in a regular exercise program * Willing to provide written informed consent

Exclusion criteria

* History of cardiovascular, pulmonary, or metabolic disease, such as hypertension or diabetes * Musculoskeletal injury or orthopedic condition preventing exercise participation * Pregnancy or breastfeeding * Smoking * Regular medication use

Design outcomes

Primary

MeasureTime frameDescription
Change in Maximal Oxygen Uptake (VO2max)Baseline and 6 weeksVO2max was assessed using a maximal exercise test on a cycle ergometer with breath-by-breath respiratory gas analysis. VO2max values were recorded in ml/kg/min before and after the 6-week intervention.

Secondary

MeasureTime frameDescription
Change in Resting Heart RateBaseline and 6 weeksResting heart rate was measured in the morning after 10 minutes of seated rest using a heart rate monitor. Values were recorded in beats per minute before and after the 6-week intervention.
Change in 6-Minute Walk Test DistanceBaseline and 6 weeksFunctional exercise capacity was assessed using the 6-minute walk test. The total distance covered in 6 minutes was recorded in meters before and after the 6-week intervention.

Countries

Turkey (Türkiye)

Contacts

PRINCIPAL_INVESTIGATORSezer Taştan, phD

Ankara Demirspor

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 23, 2026