TY - JOUR
T1 - High-intensity interval training versus moderate-intensity steady-state training in UK cardiac rehabilitation programmes (HIIT or MISS UK)
T2 - Study protocol for a multicentre randomised controlled trial and economic evaluation
AU - McGregor, Gordon
AU - Nichols, Simon
AU - Hamborg, Thomas
AU - Bryning, Lucy
AU - Tudor-Edwards, Rhiannon
AU - Markland, David
AU - Mercer, Jenny
AU - Birkett, Stefan
AU - Ennis, Stuart
AU - Powell, Richard
AU - Begg, Brian
AU - Haykowsky, Mark J.
AU - Banerjee, Prithwish
AU - Ingle, Lee
AU - Shave, Rob
AU - Backx, Karianne
N1 - Publisher Copyright:
© 2016 Published by the BMJ Publishing Group Limited.
PY - 2016/11/16
Y1 - 2016/11/16
N2 - Current international guidelines for cardiac rehabilitation (CR) advocate moderate-intensity exercise training (MISS, moderate-intensity steady state). This recommendation predates significant advances in medical therapy for coronary heart disease (CHD) and may not be the most appropriate strategy for the modern' patient with CHD. High-intensity interval training (HIIT) appears to be a safe and effective alternative, resulting in greater improvements in peak oxygen uptake (VO 2 peak). To date, HIIT trials have predominantly been proof-of-concept studies in the laboratory setting and conducted outside the UK. The purpose of this multicentre randomised controlled trial is to compare the effects of HIIT and MISS training in patients with CHD attending UK CR programmes. Methods and analysis This pragmatic study will randomly allocate 510 patients with CHD to 8weeks of twice weekly HIIT or MISS training at 3 centres in the UK. HIIT will consist of 10 high-intensity (85-90% peak power output (PPO)) and 10 low-intensity (20-25% PPO) intervals, each lasting 1min. MISS training will follow usual care recommendations, adhering to currently accepted UK guidelines (ie, >20min continuous exercise at 40-70% heart rate reserve). Outcome measures will be assessed at baseline, 8weeks and 12months. The primary outcome for the trial will be change in VO 2 peak as determined by maximal cardiopulmonary exercise testing. Secondary measures will assess physiological, psychosocial and economic outcomes. Ethics and dissemination The study protocol V.1.0, dated 1 February 2016, was approved by the NHS Health Research Authority, East Midlands-Leicester South Research Ethics Committee (16/EM/0079). Recruitment will start in August 2016 and will be completed in June 2018. Results will be published in peer-reviewed journals, presented at national and international scientific meetings and are expected to inform future national guidelines for exercise training in UK CR. Trial registration number NCT02784873; pre-results.
AB - Current international guidelines for cardiac rehabilitation (CR) advocate moderate-intensity exercise training (MISS, moderate-intensity steady state). This recommendation predates significant advances in medical therapy for coronary heart disease (CHD) and may not be the most appropriate strategy for the modern' patient with CHD. High-intensity interval training (HIIT) appears to be a safe and effective alternative, resulting in greater improvements in peak oxygen uptake (VO 2 peak). To date, HIIT trials have predominantly been proof-of-concept studies in the laboratory setting and conducted outside the UK. The purpose of this multicentre randomised controlled trial is to compare the effects of HIIT and MISS training in patients with CHD attending UK CR programmes. Methods and analysis This pragmatic study will randomly allocate 510 patients with CHD to 8weeks of twice weekly HIIT or MISS training at 3 centres in the UK. HIIT will consist of 10 high-intensity (85-90% peak power output (PPO)) and 10 low-intensity (20-25% PPO) intervals, each lasting 1min. MISS training will follow usual care recommendations, adhering to currently accepted UK guidelines (ie, >20min continuous exercise at 40-70% heart rate reserve). Outcome measures will be assessed at baseline, 8weeks and 12months. The primary outcome for the trial will be change in VO 2 peak as determined by maximal cardiopulmonary exercise testing. Secondary measures will assess physiological, psychosocial and economic outcomes. Ethics and dissemination The study protocol V.1.0, dated 1 February 2016, was approved by the NHS Health Research Authority, East Midlands-Leicester South Research Ethics Committee (16/EM/0079). Recruitment will start in August 2016 and will be completed in June 2018. Results will be published in peer-reviewed journals, presented at national and international scientific meetings and are expected to inform future national guidelines for exercise training in UK CR. Trial registration number NCT02784873; pre-results.
UR - http://www.scopus.com/inward/record.url?scp=84996865975&partnerID=8YFLogxK
U2 - 10.1136/bmjopen-2016-012843
DO - 10.1136/bmjopen-2016-012843
M3 - Article
C2 - 27852718
AN - SCOPUS:84996865975
SN - 2044-6055
VL - 6
JO - BMJ open
JF - BMJ open
IS - 11
M1 - e012843
ER -