Skip to main content
OpenTrials
Not Yet Recruiting

NCT Number: NCT07738809

Effects of Exercise Intervention on Sleep Quality and Emotional Problems in College Students With Depressive Symptoms

This exploratory randomized controlled trial aims to investigate the immediate and long-term effects of exercise on sleep quality, emotional problems, executive function, and neurophysiological characteristics in college students with depressive symptoms. The study consists of two sequential phases: an acute exercise experiment followed by an 8-week exercise intervention. Participants will be randomly assigned to either an exercise intervention group or a control group. Psychological questionnaires, behavioral tasks, resting-state electroencephalography (EEG), brain functional connectivity, and event-related potentials (ERP) will be assessed to evaluate behavioral and neurophysiological changes before and after exercise. The study will further examine whether the immediate response to acute exercise predicts the effectiveness of the long-term intervention.

Not Yet Recruiting

Trial opening soon.

Get Notified

Key information

Age range

18 year–23 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

About this study

Depressive symptoms are highly prevalent among college students and are frequently accompanied by poor sleep quality, emotional disturbances, impaired executive function, and altered brain activity. Although physical exercise has been recognized as an effective non-pharmacological intervention for improving mental health, the neurophysiological mechanisms underlying these benefits remain unclear.

This study adopts an exploratory randomized controlled design consisting of two consecutive phases. In Phase I, participants will complete a single session of low-to-moderate intensity exercise to investigate immediate changes in emotional state, executive function, resting-state EEG, brain functional connectivity, and event-related potentials (ERP). In Phase II, the same participants will continue to participate in an 8-week exercise intervention to examine the effects of regular exercise on sleep quality, depressive symptoms, emotional problems, executive function, and neurophysiological characteristics.

Behavioral assessments, standardized psychological questionnaires, resting-state EEG, brain functional connectivity analysis, and ERP recordings will be performed before and after intervention. The study will also investigate whether the immediate response to acute exercise is associated with subsequent improvements following long-term exercise intervention, providing evidence for individualized exercise prescriptions and neurophysiological mechanisms of exercise in college students with depressive symptoms.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • • Aged 18-23 years.
  • Right-handed.
  • Non-physical education major.
  • No history of psychiatric disorders and no current or previous use of psychotropic medications, hypnotics, or other medications affecting the central nervous system.
  • No history of traumatic brain injury or chronic physical diseases.
  • No contraindications to physical exercise.
  • Participants with a Beck Depression Inventory-II (BDI-II) score >13 will be classified as having depressive symptoms, whereas participants with a BDI-II score ≤13 will be classified as having no depressive symptoms.

Exclusion criteria

  • Vigorous physical exercise, alcohol consumption, caffeine intake, or other stimulating behaviors within 24 hours before testing.
  • Withdrawal from the study before completion of EEG recording or behavioral task assessments.
  • Participants will be excluded from the final analysis if they fail to complete the required questionnaires or if the collected data do not meet predefined quality control criteria.

Treatment and study plan

Archery Exercise

Behavioral

Participants perform a standardized archery exercise program consisting of an acute exercise session followed by an 8-week supervised training program. The acute session includes a 5-minute warm-up, 20 minutes of archery exercise, and a 5-minute cool-down. The long-term intervention is conducted three times per week for 8 weeks at moderate exercise intensity.

Non-exercise control

Behavioral

Participants continue their usual daily activities without participating in the archery exercise intervention.

Primary outcomes

  1. Depressive symptoms measured by the Beck Depression Inventory-II (BDI-II)

    Time frame: Baseline, immediately after the acute exercise session, and after completion of the 8-week intervention.

    Depressive symptoms will be assessed using the Beck Depression Inventory-II (BDI-II). Changes in depressive symptom severity following acute and long-term archery exercise interventions will be evaluated.

  2. Sleep quality measured by the Pittsburgh Sleep Quality Index (PSQI)

    Time frame: Baseline, immediately after the acute exercise session, and after completion of the 8-week intervention.

    Sleep quality will be assessed using the Pittsburgh Sleep Quality Index (PSQI). Changes in sleep quality after acute and long-term archery exercise interventions will be evaluated.

  3. Resting-state EEG functional connectivity

    Time frame: Baseline, immediately after the acute exercise session, and after completion of the 8-week intervention.

    Resting-state EEG functional connectivity will be analyzed using phase synchronization metrics to evaluate neural changes associated with archery exercise interventions.

Study contacts

Contact information is provided by the study sponsor or research team.

Yongguo Zhu, Professor

CONTACT

[email protected]

+86 13811265116

Sponsors and collaborators

Lead sponsor

Capital University of Physical Education and Sports, China

Other

Registry information

Official study title

Effects of Exercise Intervention on Sleep Quality, Emotional Problems, and Neuroelectrophysiological Mechanisms in College Students With Depressive Symptoms

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Jul 31, 2026
Registry last updated
Jul 31, 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.

Published trials that share one or more normalized conditions with this study.