Effect of high-intensity exercise on cardiorespiratory fitness, cardiovascular disease risk and disease activity in patients with inflammatory joint disease: protocol for the ExeHeart randomised controlled trial.


Journal

BMJ open
ISSN: 2044-6055
Titre abrégé: BMJ Open
Pays: England
ID NLM: 101552874

Informations de publication

Date de publication:
17 Feb 2022
Historique:
entrez: 18 2 2022
pubmed: 19 2 2022
medline: 21 4 2022
Statut: epublish

Résumé

Inflammatory joint disease (IJD) is associated with increased risk of cardiovascular disease (CVD) fostered by systemic inflammation and a high prevalence of CVD risk factors. Cardiorespiratory fitness (CRF) is an important health parameter and CRF-measures are advocated in routine health evaluations. CRF associates with CVD risk, and exercise modalities such as high intensity interval training (HIIT) can increase CRF and mitigate CVD risk factors. In IJD, exercise is rarely used in CVD risk management and the cardioprotective effect of HIIT is unclear. Furthermore, the clinical applicability of HIIT to primary care settings is largely unknown and warrants investigation. The primary aim is to assess the effect of a HIIT programme on CRF in patients with IJD. Second, we will evaluate the effect of HIIT on CVD risk and disease activity in patients with IJD, feasibility of HIIT in primary care and validity of non-exercise algorithms to detect change in CRF. ExeHeart is a single-blinded, randomised controlled trial. Sixty patients with IJD will be recruited from the Preventive Cardio-Rheuma clinic at Diakonhjemmet Hospital, Norway. Patients will be assigned to receive standard care (relevant lifestyle advice and cardio-preventive medication) or standard care plus a 12-week HIIT intervention by physiotherapists in primary care. HIIT sessions will be prescribed at 90%-95% of peak heart rate. Outcomes include CRF (primary outcome), CVD risk factors, anthropometric measures, disease activity and patient-reported outcomes related to pain, fatigue, disease, physical activity and exercise and will be assessed at baseline, 3 months (primary endpoint) and 6 months postbaseline. Ethical approval has been obtained from the Regional Committee for Medical and Health Research Ethics (201227). Participants are required to sign a written informed consent form. Results will be discussed with patient representatives, submitted to peer-reviewed journals and presented at relevant platforms. NCT04922840.

Identifiants

pubmed: 35177467
pii: bmjopen-2021-058634
doi: 10.1136/bmjopen-2021-058634
pmc: PMC8860070
doi:

Banques de données

ClinicalTrials.gov
['NCT04922840']

Types de publication

Clinical Trial Protocol Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e058634

Informations de copyright

© Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: AGS has received lecture honoraria from AbbVie, Novartis, Bayer, Eli Lilly and Sanofi. AGS is secretary of ESC Cardiovascular Pharmacotherapy working group, nucleus member of EACP Risk Factor Management and Primary care and steering committee member for ATACC-RA, all gratuitous. GSM has received lecture honoraria from Novartis. JH has received lecture honoraria from Amgen. KRN, HD, KV, JSe, CF, JSk, TB and ATT have nothing to disclose.

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Auteurs

Kristine Røren Nordén (KR)

Norwegian National Advisory Unit on Rehabilitation in Rheumatology, Division of Rheumatology and Research, Diakonhjemmet Hospital, Oslo, Norway kristineroren.norden@diakonsyk.no.
Institute of Health and Society, Faculty of Medicine, University of Oslo, Oslo, Norway.

Hanne Dagfinrud (H)

Norwegian National Advisory Unit on Rehabilitation in Rheumatology, Division of Rheumatology and Research, Diakonhjemmet Hospital, Oslo, Norway.
Institute of Health and Society, Faculty of Medicine, University of Oslo, Oslo, Norway.

Anne Grete Semb (AG)

Preventive Cardio-Rheuma Clinic, Division of Rheumatology and Research, Diakonhjemmet Hospital, Oslo, Norway.

Jonny Hisdal (J)

Department of vascular surgery, University of Oslo Faculty of Medicine, Oslo, Norway.

Kirsten K Viktil (KK)

Department of Pharmacy, University of Oslo, Oslo, Norway.
Diakonhjemmet Hospital Pharmacy, Diakonhjemmet Hospital, Oslo, Norway.

Joseph Sexton (J)

Division of Rheumatology and Research, Diakonhjemmet Hospital, Oslo, Norway.

Camilla Fongen (C)

Norwegian National Advisory Unit on Rehabilitation in Rheumatology, Division of Rheumatology and Research, Diakonhjemmet Hospital, Oslo, Norway.

Jon Skandsen (J)

Patient advisory board, Division of Rheumatology and Research, Diakonhjemmet Hospital, Oslo, Norway.

Thalita Blanck (T)

Patient advisory board, Division of Rheumatology and Research, Diakonhjemmet Hospital, Oslo, Norway.

George S Metsios (GS)

Department of Nutrition and Dietetics, University of Thessaly, Volos, Thessaly, Greece.

Anne Therese Tveter (AT)

Norwegian National Advisory Unit on Rehabilitation in Rheumatology, Division of Rheumatology and Research, Diakonhjemmet Hospital, Oslo, Norway.

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