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Effect of supplemental hydrocortisone during stress in prednisolone-induced adrenal insufficiency: a study protocol for a multicentre, randomised, double-blinded, placebo-controlled clinical trial on health-related quality of life in patients with polymyalgia rheumatica/giant cell arteritis on low-dose prednisolone treatment (the RESCUE study)

  • SW Borresen
  • , SB Hansen
  • , H Al-Jorani
  • , R Tei
  • , AF Dreyer
  • , VB Boesen
  • , LS Bislev
  • , NT Jorgensen
  • , RC Jensen
  • , MLL Bjergstrom
  • , LL Christensen
  • , JSS Frederiksen
  • , D Glintborg
  • , JB Bjorner
  • , U Feldt-Rasmussen
  • , JOL Jorgensen
  • , MS Andersen
  • , M Klose
  • Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark
  • Aarhus University Hospital, Aarhus, Denmark.
  • Aarhus University
  • Odense University Hospital, Odense, Denmark.
  • University of Southern Denmark
  • University of Copenhagen
  • IQVIA Inc.

Research output: Contribution to journalJournal articleResearchpeer-review

Abstract

Introduction: Patients on low-dose prednisolone may develop adrenal insufficiency causing reduced health-related quality of life (HRQoL) and increased risk of adrenal crisis. This study examines whether supplemental hydrocortisone during mild to moderate stress improves HRQoL in patients with polymyalgia rheumatica/giant cell arteritis (PMR/GCA) with adrenal insufficiency on low-dose prednisolone. Methods and analysis: A multicentre, randomised, double-blinded, placebo-controlled, clinical trial including patients with PMR/GCA receiving ongoing prednisolone = 3 months intervention period. Patients continue prednisolone tapering according to PMR/GCA guidelines. In the event of severe stress (risk of adrenal crisis), patients receive open-label hydrocortisone treatment. 95 patients with stimulated cortisol >= 420 nmol/L serve as control group. The primary outcome is HRQoL measured as fatigue using ecological momentary assessments (EMA) of the General Fatigue scale from the Multidimensional Fatigue Inventory-20, five times daily in situations of stress ('sick-days'). EMA will be administered via a smartphone application 'EMA live'. Differences in mean fatigue scores during sick-days between hydrocortisone and placebo will be analysed using mixed models for repeated measures. Secondary outcomes include daily smartphone-based symptom reporting, additional HRQoL questionnaires, adrenal crises, adverse effects from glucocorticoid excess, serial ACTH tests and biomarkers of adrenal insufficiency. Ethics and dissemination: The study is approved by the Ethics Committee of the Capital Region of Denmark and the Danish Medicines Agency. Recruitment began June 2022. The last patient's last visit is expected in 2026. Results will be disseminated via peer-reviewed publication and conference presentations.
Original languageEnglish
Article numbere113110
JournalBMJ Open
Volume16
Issue number6
ISSN2044-6055
DOIs
Publication statusPublished - 11 Jun 2026

Keywords

  • Aged
  • Female
  • Humans
  • Male
  • Adrenal Insufficiency/chemically induced
  • Double-Blind Method
  • Giant Cell Arteritis/drug therapy
  • Glucocorticoids/adverse effects
  • Hydrocortisone/administration & dosage
  • Multicenter Studies as Topic
  • Polymyalgia Rheumatica/drug therapy
  • Prednisolone/adverse effects
  • Quality of Life
  • Randomized Controlled Trials as Topic
  • Stress, Psychological

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