- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07756879
Classroom Exercise Frequency and Mental Health in Medical Students
5. august 2026 oppdatert av: Dynamical Business and Science Society - DBSS International SAS
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.
Studieoversikt
Status
Fullført
Forhold
Intervensjon / Behandling
Detaljert beskrivelse
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.
Studietype
Intervensjonell
Registrering (Faktiske)
105
Fase
- Ikke aktuelt
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiesteder
-
-
Risaralda Department
-
Pereira, Risaralda Department, Colombia, 660003
- Faculty of Health Sciences, Universidad Tecnologica de Pereira
-
-
Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Barn
- Voksen
- Eldre voksen
Tar imot friske frivillige
Ja
Beskrivelse
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.
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Forebygging
- Tildeling: Ikke-randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: 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.
|
|
Eksperimentell: 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.
|
|
Ingen inngripen: CG - Usual Classroom Activities
Thirty-three participants continued usual classroom activities and received no study exercise sessions during the 16-week period.
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Change in anxiety symptom score assessed with the DASS-21 anxiety subscale
Tidsramme: 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
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Change in depression symptom score assessed with the DASS-21 depression subscale
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
|
Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Etterforskere
- Hovedetterforsker: Jhonatan Gonzalez-Santamaria, PhD, Universidad Tecnológica de Pereira
Publikasjoner og nyttige lenker
Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.
Generelle publikasjoner
- Craig CL, Marshall AL, Sjostrom M, Bauman AE, Booth ML, Ainsworth BE, Pratt M, Ekelund U, Yngve A, Sallis JF, Oja P. International physical activity questionnaire: 12-country reliability and validity. Med Sci Sports Exerc. 2003 Aug;35(8):1381-95. doi: 10.1249/01.MSS.0000078924.61453.FB.
- Ruiz FJ, Garcia-Martin MB, Suarez-Falcon JC, Odriozola-Gonzalez P. The hierarchical factor structure of the Spanish version of Depression Anxiety and Stress Scale-21. Int J Psychol Psychol Ther. 2017;17(1):97-105.
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart (Faktiske)
3. august 2025
Primær fullføring (Faktiske)
28. november 2025
Studiet fullført (Faktiske)
28. november 2025
Datoer for studieregistrering
Først innsendt
5. august 2026
Først innsendt som oppfylte QC-kriteriene
5. august 2026
Først lagt ut (Faktiske)
11. august 2026
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
11. august 2026
Siste oppdatering sendt inn som oppfylte QC-kriteriene
5. august 2026
Sist bekreftet
1. august 2026
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- UTP-151-101224
- 28871 (Annet stipend/finansieringsnummer: Universidad Tecnológica de Pereira)
- 151-101224 (Annen identifikator: Research Ethics Committee approval)
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
JA
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Nei
Studerer et amerikansk FDA-regulert enhetsprodukt
Nei
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