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Exercise for Mental Health in Medical Students: The UNSW MedEx Project

Effect of structured exercise on psychological distress among undergraduate medical students

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12615000404527
Acronym
MedEx
Enrollment
120
Registered
2015-04-30
Start date
2015-04-06
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

This project aims to determine the feasibility and acceptability of a brief, individualized and supervised exercise intervention to improve symptoms of depression, anxiety and stress among medical students. The project will also evaluate the effect of the intervention on key measures of physical health including weight, waist circumference, aerobic exercise capacity (fitness), muscle strength and sleep behavior. The project will randomly allocate participants to either one of three experimental groups aerobic exercise, resistance exercise or an active control condition where participants will receive a ‘Jawbone’ or similar physical activity monitor for a period of eight weeks.

Interventions

Arm 1: Supervised high intensity aerobic interval training participants randomized to the aerobic interval group will attend the CSEP labs 2 x per week for 15 minutes for 8 weeks. Participants in this group will complete an aerobic training session on the stationary bike incorporating 5 x 1 minute maximum effort (rate of perceived exertion 15- 18/20) cycling bouts, with one minute active low intensity (RPE 8-9) recovery between each bout. Each session will be preceded by a warm up and followed b

Arm 1: Supervised high intensity aerobic interval training participants randomized to the aerobic interval group will attend the CSEP labs 2 x per week for 15 minutes for 8 weeks. Participants in this group will complete an aerobic training session on the stationary bike incorporating 5 x 1 minute maximum effort (rate of perceived exertion 15- 18/20) cycling bouts, with one minute active low intensity (RPE 8-9) recovery between each bout. Each session will be preceded by a warm up and followed by a cool down. Sessions will be supervised an Accredited Exercise Physiologist (AEP). Sessions will be one-on-one. Arm 2: Progressive resistance training (PRT) Participants randomised to the PRT group will attend the university training laboratory located on Ground Floor of the Wallace Wurth Building, University of NSW. Participants will exercise 2 times per week for approximately 15 minutes each visit for 8 weeks. Training will be fully supervised by an AEP to maintain proper intensity and progression, as well as to ensure correct technique. All PRT participants will receive weight lifting exercises of 5 major muscle groups using resistance equipment located in the CSEP lab. Exercises chosen include the large muscle groups of the chest, upper back and upper leg and include the cable chest press, standing cable row and leg press. These are symmetrical exercises and functionally relevant to activities of daily living (ADLs). Participants will perform 3 sets of 8 repetitions of each exercise, with controlled concentric and eccentric phases. The initial intensity for this treatment group will be set at 50% of the participant’s peak strength determined at baseline (1 repetition maximum or 1RM). Intensity will then be increased by 10% each session over 4 sessions until 80% 1RM has been reached, as we have done in previous trials of adults. Repetition maximum testing will be repeated at 2-week intervals to ascertain progress and intensity will be adjusted accordingly (usually ˜3% per session) and fine-tuned by a rating of between 15-18 on the BORG Rating of Perceived Exertion Scale. This will ensure maintenance of an intensity of 80% of the subject’s current 1RM on a continuous basis throughout the 8 week training program. Sessions will be one-on-one. Arm 3: Active control Participants who are randomised to the active control will be given the current National Physical Activity guidelines of completing 10,000 steps per day. Steps will be measured by a Jawbone or similar physical activity device and recorded/synced at a twice weekly visit with an AEP located in the Clinical Skills Exercise Physiology (CSEP) Lab. This will ensure equal contact exposure to the supervised intervention groups. Face-to-face contact will be one-on-one.

Sponsors

University of New South Wales
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Single group
Primary purpose
Prevention
Masking
Blinded (masking used) (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Participants must be ambulatory Participants must be willing to provide written informed consent Participants must be willing to participate in the study and comply with the study requirements over 10 weeks

Exclusion criteria

Those with current alcohol or substance abuse; Persons unable to comply with study requirements over the course of 10 weeks (including baseline and final assessments); Persons currently undertaking a resistance training or other regular (at least 3 days per week) moderate to high intensity exercise of any kind; Persons with specific contraindications to resistance or high intensity aerobic training exercise such as unstable cardiovascular disease, aortic aneurysm, symptomatic hernias, proliferative diabetic retinopathy, retinal laser surgery within 6 weeks, uncontrolled hypertension or rapidly progressive or terminal illness; Persons on psychotropic drugs or currently undertaking psychological interventions to control stress, anxiety and/or depression.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026