Classroom Exercise Frequency and Mental Health in Medical Students

Promoción de la Actividad física y la Salud Mental en Estudiantes de Medicina

This 16-week, three-group, nonrandomized interventional study evaluated whether the weekly frequency of a brief classroom-based physical exercise program was associated with changes in mental health and physical activity among 105 undergraduate medical students at Universidad Tecnologica de Pereira, Colombia. EG2 (n=35) received two exercise sessions per week, EG1 (n=37) received one session per week, and CG (n=33) received no exercise intervention. Anxiety, depression, stress, and physical activity were assessed at baseline and after 16 weeks.

Study Overview

Detailed Description

The three groups were specified prospectively in the ethics-approved protocol. Participation was voluntary, and all participants completed written informed consent. Academic groups were formed independently of the investigators by the university Registration and Academic Control Unit through its routine enrollment process. Both intervention groups received the same approximately 10-minute classroom exercise program and differed only in weekly frequency. Each session comprised a 3-minute warm-up, a 5-minute interval circuit involving large muscle groups, and a 2-minute cool-down with stretching and breathing. Exercises varied across sessions and intensity increased progressively. The target intensity was 5 to 7 on the modified 0-to-10 Borg scale together with a moderate Talk Test response. Attendance was called before each session by the assigned instructor, and withdrawal during a session was recorded. Adherence was defined as attendance at 80% or more of delivered sessions. No adverse events were recorded.

Study Type

Interventional

Enrollment (Actual)

105

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Risaralda Department
      • Pereira, Risaralda Department, Colombia, 660003
        • Faculty of Health Sciences, Universidad Tecnologica de Pereira

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Enrollment in the corresponding academic group (EG2, EG1, or CG) at Universidad Tecnologica de Pereira.
  • Voluntary agreement to participate and completion of written informed consent.

Exclusion Criteria:

- Medical conditions that precluded participation in physical exercise.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: EG2 - Classroom Exercise Twice Weekly
Thirty-five participants received two approximately 10-minute classroom exercise sessions per week for 16 weeks, corresponding to 32 delivered sessions.
Approximately 10-minute sessions comprising a 3-minute warm-up, a 5-minute interval circuit involving large muscle groups, and a 2-minute cool-down. Exercises varied and intensity increased progressively, targeting 5 to 7 on the modified 0-to-10 Borg scale and a moderate Talk Test response. The program required no exercise equipment.
Experimental: EG1 - Classroom Exercise Once Weekly
Thirty-seven participants received one approximately 10-minute classroom exercise session per week for 16 weeks, corresponding to 16 delivered sessions.
Approximately 10-minute sessions comprising a 3-minute warm-up, a 5-minute interval circuit involving large muscle groups, and a 2-minute cool-down. Exercises varied and intensity increased progressively, targeting 5 to 7 on the modified 0-to-10 Borg scale and a moderate Talk Test response. The program required no exercise equipment.
No Intervention: CG - Usual Classroom Activities
Thirty-three participants continued usual classroom activities and received no study exercise sessions during the 16-week period.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in anxiety symptom score assessed with the DASS-21 anxiety subscale
Time Frame: Baseline and post-intervention at week 16
Seven items are summed without doubling to obtain a raw score from 0 to 21. Higher scores indicate greater anxiety symptom severity.
Baseline and post-intervention at week 16

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in depression symptom score assessed with the DASS-21 depression subscale
Time Frame: Baseline and post-intervention at week 16
Seven items are summed without doubling to obtain a raw score from 0 to 21. Higher scores indicate greater depression symptom severity.
Baseline and post-intervention at week 16
Change in psychological stress score assessed with the DASS-21 stress subscale
Time Frame: Baseline and post-intervention at week 16
Seven items are summed without doubling to obtain a raw score from 0 to 21. Higher scores indicate greater stress symptom severity.
Baseline and post-intervention at week 16
Change in total physical activity assessed with the short-form International Physical Activity Questionnaire
Time Frame: Baseline and post-intervention at week 16
Total physical activity is expressed as MET-minutes/week by summing walking, moderate-intensity, and vigorous-intensity activity. Higher values indicate a greater physical activity volume.
Baseline and post-intervention at week 16

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Jhonatan Gonzalez-Santamaria, PhD, Universidad Tecnológica de Pereira

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

August 3, 2025

Primary Completion (Actual)

November 28, 2025

Study Completion (Actual)

November 28, 2025

Study Registration Dates

First Submitted

August 5, 2026

First Submitted That Met QC Criteria

August 5, 2026

First Posted (Actual)

August 11, 2026

Study Record Updates

Last Update Posted (Actual)

August 11, 2026

Last Update Submitted That Met QC Criteria

August 5, 2026

Last Verified

August 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • UTP-151-101224
  • 28871 (Other Grant/Funding Number: Universidad Tecnológica de Pereira)
  • 151-101224 (Other Identifier: Research Ethics Committee approval)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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