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NCT06554665Recruiting

Powering Up Stroke Rehabilitation Through HIIT

Powering Up Stroke Rehabilitation Through High-Intensity Interval Training

Source: ClinicalTrials.gov · Last updated 21 Sept 2026

Brief summary (registry, in English)

Objectives: To investigate the effects of high-intensity interval training (HIIT) on musculoskeletal fitness in chronic stroke survivors. Hypothesis to be tested: HIIT, performed on a recumbent stepper, will significantly enhance muscle power in chronic stroke survivors when compared with moderate-intensity continuous training (MICT) Design and subjects: Assessor-blinded, stratified, randomised, placebo-controlled clinical trial involving eligible 66 chronic stroke survivors. Interventions: Participants will be randomly allocated to one of three groups: the HIIT group, the MICT group, or a stretching group (active control). Each group will attend sessions three times per week for 12 consecutive weeks, totaling 36 training sessions. Main outcome measures: Assessments will be conducted at baseline, at mid-term of the intervention (week 6), at the end of the intervention (week 12), and at a 12-week follow-up (week 24). The primary outcome measure will be muscle power. Secondary outcome measures will include muscle strength, body composition, biomarkers, motor function, balance function, cardiorespiratory response, and psychosocial response.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
66 (estimated)
First submitted
30 Jul 2024
Start date
20 Aug 2024
Primary completion date
5 Aug 2027
Lead sponsor
The Hong Kong Polytechnic University
Diseases
Stroke
NCT number
NCT06554665

What you commit to

  • Study type: Interventional
  • Planned participants: 66
  • From 20 Aug 2024 to the primary completion date, 5 Aug 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Undergoing osteoporosis treatments within the past 3 years, use of oral corticosteroids for more than 3 months within the past year, or botulinum toxin injections in the paretic lower limb within the past 6 months

Other illness

  • Presence of other neurological comorbidities, significant liver or renal diseases, thyroid or parathyroid diseases, rheumatoid arthritis, or a fracture within the past 6 months
  • Participation in ongoing stroke rehabilitation services or structured exercise programme

Lab values

  • Contraindications to HIIT, graded exercise testing, or failure to pass medical clearance from a specialist

Other

  • Cognitive or communication issues that could limit the ability to follow instructions

Who the study is looking for

  • Men and postmenopausal women aged 50-80 years
  • 1-5 years following the first-ever stroke confirmed by magnetic resonance imaging or computed tomography
  • Able to walk 10 meters independently with or without a walking aid
  • Class I or II according to the New York Heart Association Functional Classification (no limitation or slight limitation of physical activity due to symptoms during ordinary physical activity)

Age in the registry: 50 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
The Hong Kong Polytechnic University
Coordinator of this site? Confirm its status
KowloonHong Kong SAR ChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.