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HIIT the Gym: The effects of High Intensity Interval Training (HIIT) on improving fatigue in Multiple Sclerosis

HIIT the Gym: The effects of High Intensity Interval Training (HIIT) on improving fatigue in Multiple Sclerosis – a metabolomics and microbial study

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12626000145303
Enrollment
66
Registered
2026-02-05
Start date
2026-07-01
Completion date
2028-04-01
Last updated
2026-02-09

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

Conditions

None listed

Brief summary

The study examines the effects of an 8-week high-intensity interval training (HIIT) program, involving two 30-minute sessions per week, in two groups of people with multiple sclerosis—those with high and low levels of fatigue. The aim is to measure changes in fatigue, cognitive function, and biological processes related to metabolism and gut microbiome diversity. It is expected that both groups will show benefits from the program, but that the extent and pattern of improvement will differ depending on participants’ baseline fatigue levels.

Interventions

The intervention is High-Intensity Interval Training (HIIT) using stationary cycle ergometry conducted in people with multiple sclerosis. Participants are stratified into high-fatigue and low-fatigue groups based on age- and education-adjusted Modified Fatigue Impact Scale (MFIS) cut-off scores; however, all participants receive the same intervention protocol. Materials required for the intervention include stationary cycle ergometers (Fluid E750 Cycle Body Trainer) and Polar H10 heart-rate mon

The intervention is High-Intensity Interval Training (HIIT) using stationary cycle ergometry conducted in people with multiple sclerosis. Participants are stratified into high-fatigue and low-fatigue groups based on age- and education-adjusted Modified Fatigue Impact Scale (MFIS) cut-off scores; however, all participants receive the same intervention protocol. Materials required for the intervention include stationary cycle ergometers (Fluid E750 Cycle Body Trainer) and Polar H10 heart-rate monitors for continuous heart-rate monitoring. The intervention procedure involves participants attending supervised HIIT cycling sessions for 8 weeks (two 30-minute sessions per week; 16 sessions total). Each session begins with a 5-minute warm-up at low intensity, followed by 10 repeated cycles of 90 seconds of high-intensity cycling and 30 seconds of moderate-intensity cycling for active recovery. Each session concludes with a 5-minute cool-down at low intensity. The session structure, prescribed intensity zones, and cycling cadence are standardised across participants. High-intensity intervals target a Borg Rating of Perceived Exertion (RPE) of 15–19, corresponding to approximately 85–95% of age-predicted maximal heart rate (HRmax), while moderate-intensity intervals target an RPE of 12–14, corresponding to approximately 60–75% HRmax. Cycling cadence is standardised at approximately 80–100 revolutions per minute during high-intensity intervals and 60–80 revolutions per minute during moderate-intensity intervals. Cycling resistance is adjusted individually for each participant to achieve the target intensity. Sessions are delivered face-to-face on a one-to-one basis by tertiary-qualified Exercise Physiologists with experience in neurological and multiple sclerosis rehabilitation. Absolute workload (e.g. cycling resistance) is individualised and adjusted within or between sessions by the Exercise Physiologist based on continuous heart-rate monitoring, RPE ratings, fatigue, and clinical presentation to safely maintain the intended relative intensity of the intervention. All sessions are conducted within an outpatient clinical setting in a rehabilitation gym located in Sydney, Australia. Exercise intensity and intervention fidelity are monitored during each session using continuous heart-rate monitoring (Polar H10) and repeated RPE ratings recorded by the supervising Exercise Physiologist. Adherence is assessed as the proportion of prescribed sessions attended, calculated as the percentage of completed sessions out of the total 16 scheduled sessions. Any protocol deviations, intensity adjustments, or adverse events are documented in standardised session records.

Sponsors

Macquarie University
Lead SponsorUniversity

Study design

Allocation
Non-randomised trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

people with a formal diagnosis of relapsing-remitting multiple sclerosis (RRMS) by a clinician, aged 18–50 years, with mild to moderate disability (EDSS score of 2-6). These criteria represent the largest proportion of individuals living with MS.

Exclusion criteria

Cardiovascular/neurological disorders (e.g. strokes, epilepsy, brain injury), substance abuse or other health complications, involved in physical therapy treatment at the time of recruitment, acute exacerbation of symptoms 4 weeks prior to assessment, diagnosis of psychotic, bipolar or related disorder and use of DMD: corticosteroid use in the last 4 weeks or immune-suppressive therapy in the last 6 months.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 15, 2026