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Clinical Trial NCT07494552 for Sport Participation is not yet recruiting. See the Trial Radar Card View and AI discovery tools for all the details. Or ask anything here.
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Running Environments on Physiological Responses, Emotion, Motivation, and Attention 30 Exercise-Based

Not yet recruiting
Clinical Trial NCT07494552 is an interventional study for Sport Participation and is currently not yet recruiting. Enrollment is planned to begin on 10 April 2026 and continue until the study accrues 30 participants. Led by Shanghai University of Sport, this study is expected to complete by 10 June 2026. The latest data from ClinicalTrials.gov was last updated on 27 March 2026.
Brief Summary
The goal of this clinical trial is to learn how different running environments affect physiological responses, emotional regulation, exercise motivation, and attentional control in healthy college students. The main questions it aims to answer are:

How do different running environments (indoor treadmill, outdoor road, and outdoor grass) affect physiological stress and recovery, such as heart rate variability, blood ...

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Detailed Description
This study employs a randomized, counterbalanced crossover design to investigate the acute effects of three different running environments (indoor treadmill, outdoor road, and outdoor grass) on physiological, psychological, and cognitive outcomes. Each of the 30 healthy college student participants will complete three experimental sessions corresponding to the three environments. To eliminate carry-over effects and f...Show More
Official Title

Effects of Different Running Environments on Individual Physiological Responses, Emotion Regulation, Exercise Motivation, and Attentional Control

Conditions
Sport Participation
Other Study IDs
  • 102772025RT192
NCT ID Number
Start Date (Actual)
2026-04-10
Last Update Posted
2026-03-27
Completion Date (Estimated)
2026-06-10
Enrollment (Estimated)
30
Study Type
Interventional
PHASE
N/A
Status
Not yet recruiting
Primary Purpose
Basic Science
Design Allocation
Randomized
Interventional Model
Crossover Assignment
Masking
Single
Arms / Interventions
Participant Group/ArmIntervention/Treatment
ExperimentalIndoor Treadmill Running
Participants will complete a 20-minute moderate-intensity running session on a treadmill in a controlled indoor sports venue.
Indoor Treadmill Running Session
20 minutes of moderate-intensity running on an indoor treadmill. Exercise intensity is monitored and controlled using heart rate devices to maintain a consistent moderate level.
ExperimentalOutdoor Road Running
Participants will complete a 20-minute moderate-intensity running session on a standard outdoor campus athletic track.
Outdoor Road Running Session
20 minutes of moderate-intensity running on an outdoor athletic track (paved surface).
ExperimentalOutdoor Grass Running
Participants will complete a 20-minute moderate-intensity running session on a natural campus lawn/grass area.
Outdoor Grass Running Session
20 minutes of moderate-intensity running on a natural grass surface.
Primary Outcome Measures
Outcome MeasureMeasure DescriptionTime Frame
Change in Salivary Cortisol Concentration
Salivary cortisol concentration will be measured to evaluate the acute endocrine and physiological stress response to different running environments.
Baseline (pre-exercise) and 20 minutes post-exercise.
Secondary Outcome Measures
Outcome MeasureMeasure DescriptionTime Frame
Change in Heart Rate Variability (HRV)
Heart Rate Variability (HRV) parameters, specifically RMSSD and SDNN, will be recorded to assess the acute autonomic nervous system responses and recovery. Both parameters share the exact same unit of measure, which is milliseconds (ms).
Baseline (pre-exercise), immediately post-exercise, 5 minutes post-exercise, 10 minutes post-exercise, and 20 minutes post-exercise.
Change in Systolic and Diastolic Blood Pressure
Blood pressure will be measured in mmHg to evaluate the cardiovascular stress response across different running environments.
Baseline (pre-exercise), immediately post-exercise, 5 minutes post-exercise, 10 minutes post-exercise, and 20 minutes post-exercise.
Change in Blood Lactate Concentration
Blood lactate will be measured using a portable analyzer to assess metabolic exertion.
Baseline (pre-exercise) and immediately post-exercise.
Inhibitory Control Assessed by the Stroop Task: Reaction Time
The Stroop task measures inhibitory control and cognitive interference. This measure reports the reaction time in milliseconds (ms). Lower reaction times indicate better inhibitory control.
Baseline (pre-exercise) and 20 minutes post-exercise.
Response Inhibition Assessed by the Go/No-Go Task: Reaction Time
The Go/No-Go task is used to evaluate response inhibition and impulse control. This measure reports the reaction time in milliseconds (ms) for "Go" trials. Lower values indicate faster processing speed.
Baseline (pre-exercise) and 20 minutes post-exercise.
Change in Heart Rate
Heart rate will be monitored and recorded in beats per minute (bpm) to assess cardiovascular exertion during the intervention and the subsequent recovery rate.
Baseline (pre-exercise), immediately post-exercise, 5 minutes post-exercise, 10 minutes post-exercise, and 20 minutes post-exercise.
Mood State Assessed by Positive and Negative Affect Schedule (PANAS)
The Positive and Negative Affect Schedule (PANAS) consists of two subscales to measure both positive affect (10 items) and negative affect (10 items) reflecting the past week. Items are rated on a 5-point scale. For the Positive Affect subscale, the minimum possible score is 10 and the maximum possible score is 50, with higher scores indicating higher levels of positive emotions (a better outcome). For the Negative Affect subscale, the minimum possible score is 10 and the maximum possible score is 50, with higher scores indicating higher levels of negative emotions (a worse outcome).
Baseline (pre-exercise) and 20 minutes post-exercise.
Change in Exercise Enjoyment Assessed by Physical Activity Enjoyment Scale (PACES)
The Physical Activity Enjoyment Scale (PACES) is used to evaluate the participant's subjective enjoyment of the exercise session. The scale consists of 18 items, each rated on a 7-point scale (1=completely disagree, 7=completely agree). The total score ranges from 18 to 126. Higher scores indicate a greater level of exercise enjoyment (a better outcome).
Baseline (pre-exercise) and 20 minutes post-exercise.
Habitual Sport Motivation Assessed by Sport Motivation Scale (SMS)
The Sport Motivation Scale (SMS) is used to evaluate habitual, long-term motivation toward sports (reflecting on the past year). It consists of 28 items rated on a 7-point scale (1=does not correspond at all, 7=corresponds exactly). The total global score ranges from 28 to 196. Higher scores indicate higher levels of self-determined motivation toward sports (a better outcome).
Baseline (pre-exercise) and 20 minutes post-exercise.
Attentional Control Assessed by Attentional Control Scale (ACS)
he Attentional Control Scale (ACS) is used to assess the participant's general trait ability to control attention and focus. The scale consists of 20 items rated on a 4-point scale (1=almost never, 4=always). The total score ranges from 20 to 80. Higher scores indicate better attentional control capabilities (a better outcome).
Baseline (pre-exercise) and 20 minutes post-exercise.
Perceived Recovery Assessed by Restoration Outcome Scale (ROS)
The Restoration Outcome Scale (ROS) evaluates physical and psychological restoration through 6 items rated on a 5-point scale. The minimum possible total score is 6 and the maximum possible total score is 30. Higher scores indicate a higher level of perceived physical and psychological recovery (a better outcome).
Baseline (pre-exercise) and 20 minutes post-exercise.
Inhibitory Control Assessed by the Stroop Task: Accuracy
The Stroop task measures inhibitory control and cognitive interference. This measure reports the accuracy as a percentage (%). Higher percentages indicate better cognitive performance and fewer errors.
Baseline (pre-exercise) and 20 minutes post-exercise.
Response Inhibition Assessed by the Go/No-Go Task: Accuracy
The Go/No-Go task is used to evaluate response inhibition and impulse control. This measure reports the accuracy of responses as a percentage (%). Higher percentages indicate better impulse control and fewer false alarms.
Baseline (pre-exercise) and 20 minutes post-exercise.
Participation Assistant
Eligibility Criteria

Eligible Ages
Adult
Minimum Age
18 Years
Eligible Sexes
All
Accepts Healthy Volunteers
Yes
  • Full-time college students aged 18 to 25 years old.
  • Healthy, with no history of major cardiovascular, respiratory, neurological, or endocrine diseases.
  • No exercise contraindications or injuries, capable of safely completing moderate-intensity running (treadmill, outdoor road, and grass running).
  • No recent major life events affecting physiological or psychological status (e.g., severe insomnia, anxiety, depression, or extreme fatigue).
  • No use of medications or supplements affecting heart rate, blood pressure, mood, or attention within the past week.
  • Normal or corrected-to-normal vision, capable of completing computerized cognitive tasks (e.g., Stroop, Go/No-Go, PVT).
  • Able to comprehend and truthfully complete psychological scales.
  • Voluntary participation and signed informed consent form.

  • Current or past diagnosis of severe cardiovascular disease (e.g., myocardial infarction, severe arrhythmia, uncontrolled hypertension).
  • Severe respiratory disease (e.g., severe asthma, COPD) or recent acute respiratory infection within the past month.
  • History of neurological disease or brain injury (e.g., epilepsy, recent concussion) affecting safety or cognitive task performance.
  • Endocrine or metabolic diseases (e.g., uncontrolled thyroid disease, severe diabetes) affecting cortisol or metabolic measurements.
  • Recent diagnosis or psychiatric treatment for severe psychological disorders within the past month.
  • Use of drugs or supplements affecting heart rate, blood pressure, cortisol, or attention within the past 7 days.
  • Currently pregnant or lactating.
  • Acute illness within the past 48 hours (e.g., fever, acute gastroenteritis).
  • Severe bleeding tendencies, blood disorders, or contraindications to blood/saliva sampling.
  • Recent substance use interference, such as heavy drinking or substance dependence within the past 2 weeks.
  • Inability to meet pre-experiment control requirements (e.g., avoiding caffeine, tobacco, or heavy exercise).
  • Inability to complete computerized tasks due to poor vision or lack of familiarity with keyboard/mouse.
  • Acute or chronic injuries hindering the safe completion of running intervention (e.g., recent lower limb injury).
  • Participation in similar HIT or environmental intervention studies within the past 3 months.
  • Unable to understand research procedures or unwilling to sign the informed consent form.
Shanghai University of Sport logoShanghai University of Sport
Study Responsible Party
Zhu kun, Principal Investigator, Professor, Shanghai University of Sport
Study Central Contact
Contact: Xinyu Li, 86+18380367935, [email protected]
Contact: Shijun Jin, 86+15670976576, [email protected]
1 Study Locations in 1 Countries

Shanghai Municipality

Shanghai University of Sport, Shanghai, Shanghai Municipality, 200438, China
kun Zhu, Ph.D., Contact, 86+13817220306, [email protected]