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The Effect of High Intensity Interval Training on Cardiovascular Fitness in People With Progressive Multiple Sclerosis.

The Effect of High Intensity Interval Training on Cardiovascular Fitness in People With Progressive Multiple Sclerosis.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02950454
Enrollment
12
Registered
2016-11-01
Start date
2017-01-31
Completion date
2017-09-30
Last updated
2017-10-25

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

Conditions

Multiple Sclerosis, Progressive

Keywords

Progressive Multiple Sclerosis, Rehabilitation, Exercise

Brief summary

This is a pilot trial to explore the cardiovascular of eight weeks of twice weekly high intensity interval training in people with progressive multiple sclerosis. A control group of people with progressive multiple sclerosis will undergo continuous moderate intensity exercise, twice weekly for 8 weeks.

Detailed description

This is a pilot trial to explore the cardiovascular of eight weeks of twice weekly high intensity interval training in people with progressive multiple sclerosis. A control group of people with progressive multiple sclerosis will undergo continuous moderate intensity exercise, twice weekly for 8 weeks. The training program will entail 6x1.5 minute intervals working at 80-95% heart rate max on a cycle ergometer. Each interval will be interspersed with 1.5 minutes of working rest at a light resistance of the participant's choosing. The continuous moderate intensity exercise program will entail 20 minutes on a cycle ergometer working at 60-70% heart rate max.

Interventions

OTHERHigh intensity interval training

1.5 min intervals at 80-95% heart rate max on cycle ergometer 1.5 min intervals at nominal resistance on cycle ergometer

20 min at 60-70% heart rate max on cycle ergometer

Sponsors

NHS Ayrshire and Arran
CollaboratorOTHER
AKM
CollaboratorOTHER
University of Glasgow
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* Diagnosed with a progressive form of MS * Aged 18 years or older * Known to members of staff of the MS service NHS Ayrshire & Arran * Ability to attend Douglas Grant Rehabilitation centre twice a week for eight weeks * EDSS 4-6.0 * Able to cycle on ergometer

Exclusion criteria

* A relapse of symptoms requiring treatment within the past three months. * A respiratory condition that would be exacerbated by high intensity exercise including but not limited to: chronic obstructive pulmonary disorder, uncontrolled or poorly controlled asthma. * Uncontrolled high pressure at screening (\>190/100 mmHg) * Cognitive impairment affecting ability to understand instructions as noted in patient's notes. * Currently engaging in another research trial for their MS or that may affect their physiological or cardiovascular outcomes * Weighing more than 110 kg (weight limit of ergometer) * Any pathology or medical intervention that would preclude high intensity exercise, maximal exertion testing or could attenuate the cardiovascular effect of exercise including but not limited to: unstable angina; diabetes; peripheral vascular disease or intermittent claudication; having a pace maker or medicine pump; surgical clips; having another neurological condition other than MS; and pregnancy. To be established from patient's notes and at screening session. * A serious cardiovascular event in the past year including but not limited to: transient ischaemic attack, cerebrovascular event and myocardial infarction. * Taking any of the following medication: beta blockers; vasodilators; ACE inhibitors; diuretics or any other medication that could cause exercise induced hypotension; hypoglycaemic insulin; metformin or other oral insulin medicine.

Design outcomes

Primary

MeasureTime frameDescription
heart rate max8 weeksMaximal heart rate elicited during a maximal exertion test

Secondary

MeasureTime frameDescription
Resting heart rate8 weeks
Brain derived neurotrophic factor8 weeksHormone important for brain growth and protection
Lactate8 weeksWaste materials from exercise in blood
Lipoprotein profile8 weeksIndication of how much good and how much bad cholesterol is in blood
Resting blood pressure8 weeks
Hospital anxiety and depression scale8 weeksQuestionnaire giving a score of depression and anxiety
Timed 25 foot walk test8 weeksMeasure of walking speed
Symbol digit modalities test8 weeksMeasure of mental processing speed
Fatigue severity scale8 weeksQuestionnaire which gives measure of fatigue.
MSIS-29 version 28 weeksQuestionnaire giving physical and psychological impact of MS

Countries

United Kingdom

Outcome results

None listed

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