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Completed

NCT Number: NCT07596836

Sprint Interval Training in Young Sedentary Adults

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.

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Key information

Age range

20 year–25 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Ankara Demirspor

Ankara, 06000, Turkey (Türkiye)

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Sprint Interval Training

Behavioral

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.

Other names: SIT

Primary outcomes

  1. Change in Maximal Oxygen Uptake (VO2max)

    Time frame: Baseline and 6 weeks

    VO2max 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 outcomes

  1. Change in Resting Heart Rate

    Time frame: Baseline and 6 weeks

    Resting 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.

  2. Change in 6-Minute Walk Test Distance

    Time frame: Baseline and 6 weeks

    Functional 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.

Sponsors and collaborators

Lead sponsor

Sezer Taştan

Other

Registry information

Official study title

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

Acronym: SIT

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
May 19, 2026
Registry last updated
May 22, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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