Systemic sclerosis (SSc) is a rare autoimmune connective tissue disease associated with substantial impairments in health-related quality of life, physical function, and participation in daily activities. Although exercise is recommended as part of the non-pharmacological management of SSc, the current evidence is based primarily on small, short-term studies, and high-quality randomized controlled trials evaluating the effectiveness and cost-effectiveness of home-based exercise programmes are lacking.
The ScleroStrong trial is an international, multicentre, assessor-blinded, parallel-group randomised controlled trial conducted at Aarhus University Hospital, Odense University Hospital, Copenhagen University Hospital - Rigshospitalet, and the University Hospital of Pisa. A total of 270 adults with systemic sclerosis will be randomised (1:1) to either a partially supervised, home-based exercise programme in addition to usual care or to usual care alone. Clinical effectiveness will be evaluated at 6 months, while the health economic evaluation will be performed over a 12-month follow-up period.
The primary objective is to determine whether a partially supervised, home-based exercise programme improves health-related quality of life compared with usual care. A secondary objective is to evaluate whether the intervention represents a cost-effective treatment strategy from both societal and healthcare perspectives. The study will additionally investigate the effects of the intervention on disease impact, physical function, physical activity, depressive symptoms, adherence, and safety.
The investigators hypothesize that:
- A partially supervised, home-based exercise programme will result in greater improvements in health-related quality of life after 6 months compared with usual care.
- The partially supervised, home-based exercise programme will be cost-effective and cost-utility favourable compared with usual care over a 12-month follow-up period.
- Participants allocated to the partially supervised, home-based exercise programme will demonstrate greater improvements in disease impact, physical function, and physical activity than participants receiving usual care.
A full trial protocol including a statistical analysis plan will be published and made publicly available before completion of the primary analyses. The primary analysis will follow the intention-to-treat principle, with a supplementary per-protocol analysis. Between-group differences will be analysed using mixed-effects regression models including intervention group, follow-up time, and their interaction as fixed effects, while recruitment site and participant will be included as random effects. Cost-effectiveness and cost-utility analyses will estimate incremental cost-effectiveness ratios (ICERs) and incremental cost-utility ratios (ICURs) based on healthcare and societal costs and quality-adjusted life years.