Skip to content

Online Wellness Intervention in Medical Students

Assessing the Effectiveness of a 12-week Online Wellness Intervention in Medical Students: a Pre-Post Single-arm Interventional Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04612387
Enrollment
65
Registered
2020-11-03
Start date
2020-10-25
Completion date
2021-04-30
Last updated
2022-04-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mind Body Therapy, Stress, Psychological, Wellbeing

Brief summary

Medical students are at high risk of stress. This project will test how well a 12-week stress reduction program works to reduce stress, anxiety and depression and improve well-being. The program is delivered online and each week is made of an introduction video, 7-8 minutes of yoga, 5-7 minutes of meditation and nutrition tips. At the beginning and the end of the 12-week research study, we will be using surveys to ask students about their stress, anxiety, depression, sense of control over their own life, quality of life, and pain levels. After the program, the research team will conduct interviews with the medical student to allow them to share their other feedback about the program. The researchers will also send surveys to the medical students one month after the program ends to asses their continued satisfaction with and adherence to the program.

Interventions

Online yoga, meditation and nutrition tips.

Sponsors

University of Alberta
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

\- Medical students in any year of medical school

Exclusion criteria

* Hospital Anxiety and Depression Scale (HADS) Depression score \>10 * Active psychosis * Post-traumatic stress disorder or frequent suicidal ideation * Major medical co-morbidity * Inability to provide written informed consent

Design outcomes

Primary

MeasureTime frameDescription
Perceived Stress Scale12 weeksThe degree to which situations in one's life are appraised as stressful will be assessed using the Perceived Stress Scale. The minimum score is 0, the maximum score is 40, and higher scores indicate a worse outcome.

Secondary

MeasureTime frameDescription
Patient Health Questionnaire (PHQ-9)12 weeksThe Patient Health Questionnaire (PHQ-9) will be used to measure depression. The minimum score is 0, the maximum is 27, and higher scores indicate a worse outcome.
Psychological Wellbeing Scale12 weeksThe Psychological Wellbeing Scale will be sued to measure well being. Higher scores mean higher levels of psychological well-being
Five Facet Mindfulness Questionnaire12 weeksMindfulness will be assessed using the Five Facet Mindfulness Questionnaire.
Hospital Anxiety and Depression Scale (HADS)12 weeksDepression and anxiety will be measured on the Hospital Anxiety and Depression Scale. The minimum value is 0, the maximum is 21, and higher scores mean a worse outcome.

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026