Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Randomized Controlled Trial
. 2017 Dec 8;18(1):591.
doi: 10.1186/s13063-017-2330-8.

Does intensive management improve remission rates in patients with intermediate rheumatoid arthritis? (the TITRATE trial): study protocol for a randomised controlled trial

Collaborators, Affiliations
Randomized Controlled Trial

Does intensive management improve remission rates in patients with intermediate rheumatoid arthritis? (the TITRATE trial): study protocol for a randomised controlled trial

Naomi H Martin et al. Trials. .

Abstract

Background: Uncontrolled active rheumatoid arthritis can lead to increasing disability and reduced quality of life over time. 'Treating to target' has been shown to be effective in active established disease and also in early disease. However, there is a lack of nationally agreed treatment protocols for patients with established rheumatoid arthritis who have intermediate disease activity. This trial is designed to investigate whether intensive management of disease leads to a greater number of remissions at 12 months. Levels of disability and quality of life, and acceptability and cost-effectiveness of the intervention will also be examined.

Methods: The trial is a 12-month, pragmatic, randomised, open-label, two-arm, parallel-group, multicentre trial undertaken at specialist rheumatology centres across England. Three hundred and ninety-eight patients with established rheumatoid arthritis will be recruited. They will currently have intermediate disease activity (disease activity score for 28 joints assessed using an erythrocyte sedimentation rate of 3.2 to 5.1 with at least three active joints) and will be taking at least one disease-modifying anti-rheumatic drug. Participants will be randomly selected to receive intensive management or standard care. Intensive management will involve monthly clinical reviews with a specialist health practitioner, where drug treatment will be optimised and an individualised treatment support programme delivered based on several principles of motivational interviewing to address identified problem areas, such as pain, fatigue and adherence. Standard care will follow standard local pathways and will be in line with current English guidelines from the National Institute for Health and Clinical Excellence. Patients will be assessed initially and at 6 and 12 months through self-completed questionnaires and clinical evaluation.

Discussion: The trial will establish whether the known benefits of intensive treatment strategies in active rheumatoid arthritis are also seen in patients with established rheumatoid arthritis who have moderately active disease. It will evaluate both the clinical and cost-effectiveness of intensive treatment.

Trial registration: Current Controlled Trials, ID: ISRCTN70160382 . Registered on 16 January 2014.

Keywords: Intensive treatment; Intermediate disease activity; Randomised controlled trial; Rheumatoid arthritis; Treating to target; Tumour necrosis factor inhibitors.

PubMed Disclaimer

Conflict of interest statement

Ethics approval and consent to participate

Ethical approval for this trial was obtained from the London – West London and GTAC National Research Ethics Service (NRES) Committee (13/LO/1308). This Ethics Committee approved the study for all participating centres. All participants provide written informed consent before participating in the trial or extension study.

Consent for publication

Not applicable.

Competing interests

A list of investigators with competing interests and the details they have declared is as follows: Dr. James Galloway received consultancy fees for educational talks from UCB, Pfizer, Napp and MSD. Dr. Heidi Lempp received funding over the last 5 years from the National Institute of Health Research; European Union; Guy’s and St Thomas’ Charity, London; The Health Foundation, London; Arthritis Research UK; and the South London Membership Council. Professor Jackie Sturt received funding from Eli Lilly for consultancy activities in 2016 and will continue to do so in 2017.

Pfizer made Enbrel freely available for use outside NICE guidance in this study.

The following authors declare that they have no competing interests: Dr. Naomi Martin, Ms. Fowzia Ibrahim, Dr. Brian Tom, Professor Allan Wailoo, Mr. Jon Tosh, Ms. Louise Prothero, Dr. Sofia Georgopoulou, Professor David Scott.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Figures

Fig. 1
Fig. 1
Study design: outline of intensive management approach and standard treatment arms
Fig. 2
Fig. 2
Standard Protocol Items Recommendations for Interventional Trials (SPIRIT) Schedule of enrolment, interventions and assessments

Similar articles

Cited by

References

    1. Scott DL, Wolfe F, Huizinga TW. Rheumatoid arthritis. Lancet. 2010;376:1094–108. doi: 10.1016/S0140-6736(10)60826-4. - DOI - PubMed
    1. Pugner KM, Scott DL, Holmes JW, Hieke K. The costs of rheumatoid arthritis: an international long-term view. Semin Arthritis Rheum. 2000;29:305–20. doi: 10.1016/S0049-0172(00)80017-7. - DOI - PubMed
    1. Scott DL, Steer S. The course of established rheumatoid arthritis. Best Pract Res Clin Rheumatol. 2007;21:943–67. doi: 10.1016/j.berh.2007.05.006. - DOI - PubMed
    1. Deighton C, O’Mahony R, Tosh J, Turner C, Rudolf M, Guideline Development Group Management of rheumatoid arthritis: summary of NICE guidance. BMJ. 2009;338:b702. doi: 10.1136/bmj.b702. - DOI - PMC - PubMed
    1. Pincus T, Castrejón I, Bergman MJ, Yazici Y. Treat-to-target: not as simple as it appears. Clin Exp Rheumatol. 2012;30(4 Suppl 73):S10–20. - PubMed

Publication types

MeSH terms

Substances