- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06984900
- Original Trial
How Short-Term Aerobic Exercise Affects Stress and Mood in Students (SEAEM)
Investigating The Effect of Short-Term Aerobic Exercise on Stress and Mood Among Students
Study Overview
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
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Buraydah, Saudi Arabia, 51452
- Qassim University, in Qassim University Medical City, the Kingdom of Saudi Arabia (KSA).
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Healthy male and female students aged between 18 and 25 years.
- Ability to speak and understand written English.
Exclusion Criteria:
- Students who are pregnant or planning to become pregnant.
- Students who currently smoke.
- Students who respond "yes" to any of the seven questions on the Physical Activity Readiness Questionnaire (PAR-Q).
- Students taking medications for chronic diseases such as high blood pressure or diabetes.
- Students with a current or past diagnosis of a psychotic disorder.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Short-Term Aerobic Exercise Group
|
The Aerobic Exercise Program is designed to improve mood and reduce stress among university students through structured, moderate-intensity aerobic activities. Session Structure: Participants engage in moderate-intensity aerobic exercises such as treadmill walking or running, tailored to individual fitness levels, ensuring accessibility and inclusivity. Each session consists of a 10-minute warm-up, 30 minutes of aerobic exercise, and a 5-minute cool-down. This intervention incorporates a dual assessment approach using the Profile of Mood States (POMS) and the Perceived Stress Scale (PSS) to evaluate mood and stress levels both before and after exercise. Participants complete these assessments multiple times, allowing for a nuanced understanding of how aerobic exercise influences mood and stress over time. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Improvement in Total Mood Disturbance Following Short-Term Aerobic Exercise in University Students
Time Frame: TMD is assessed at eight time points: Before exercise (T0) Immediately after exercise (T1) At intervals: 1 hour (T2), 2 hours (T3), 4 hours (T4), 8 hours (T5), 12 hours (T6), and 24 hours post-exercise (T7).
|
Total Mood Disturbance (TMD): Measured using the Profile of Mood States (POMS) questionnaire. Scores range from 0 to a maximum depending on the number of items (65 items rated on a 0-4 Likert scale, resulting in a theoretical range of 0 to 260). A higher TMD score represents a worse overall mood outcome. |
TMD is assessed at eight time points: Before exercise (T0) Immediately after exercise (T1) At intervals: 1 hour (T2), 2 hours (T3), 4 hours (T4), 8 hours (T5), 12 hours (T6), and 24 hours post-exercise (T7).
|
|
Perceived Stress Levels Following Short-Term Aerobic Exercise in University Students
Time Frame: Assessed at two time points: Before exercise (T0) 24 hours after exercise (T7).
|
Perceived Stress Levels: Measured using the Perceived Stress Scale (PSS). Scores range from 0 to 40. Higher scores indicate higher levels of perceived stress. Scores can be categorized as: Low stress: 0-13 Moderate stress: 14-26 High stress: 27-40 |
Assessed at two time points: Before exercise (T0) 24 hours after exercise (T7).
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 24-71-12
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- CSR
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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