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Cross-condition Validation of the Steroid PRO

Cross-condition Validation of the Patient Reported Outcome Measure for Patients Receiving Glucocorticoids (the Steroid PRO)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06314451
Enrollment
60
Registered
2024-03-18
Start date
2022-06-01
Completion date
2024-05-31
Last updated
2024-03-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Inflammatory Disease, Immune System Disorder, Gastrointestinal Diseases, Dermatologic Disease, Respiratory Disease

Keywords

Glucocorticoids, Steroids, Health-related quality of life, Rheumatology, Respiratory, Gastroenterology, Dermatology, Pulmonology, Patient, Patient reported outcomes

Brief summary

Testing a questionnaire about treatment with steroids for skin, lung or gastric conditions

Detailed description

Glucocorticoid drugs, also known as 'steroids', are used to treat a range of diseases. It is well-known that steroids can cause many unwanted side-effects. The investigators are interested in measuring the impact of steroids on quality of life, from the patients' perspective. In a previous part of this study, the investigators interviewed participants treated with steroids for a range of rheumatic conditions. The participants were asked how taking steroids affects their everyday lives. A patient questionnaire (the 'Steroid PRO') was then created focused on the topics identified as being most important to participants. Now the investigators would like to test this questionnaire with new participants, aged 18 or over, who are taking steroids for other conditions. This could include participants who have inflammation in the lungs, skin, or bowels. The investigators will also ask for feedback from the medical teams who care for those who have these conditions. The study involves a single interview with a researcher, either online or by telephone. Participants who want to take part will be given information about the study and asked to give written consent. Participants will be asked to talk about the wording of the questionnaire and how relevant and feasible it is to them. This part of the study is funded by Sanofi Research and Development. The work is being carried out by independent researchers at the University of the West of England (UWE, Bristol). Participants will be recruited from hospitals in the UK and USA. The investigators hope that the Steroid PRO questionnaire will be used in future research trials about steroid treatment and alternatives to steroids. The Steroid PRO questionnaire could also be used in clinics to improve communication between clinicians and patients.

Interventions

The study involves a single cognitive interview with a researcher, either online, by telephone, or face-to-face. People who want to take part will be given information about the study and asked to give written consent. Then they will be asked to talk about the wording of the questionnaire and how relevant it is to them. Cognitive interviewing is recognized as a significant part of developing questionnaires for patient reported outcome measures (PROMs). The cognitive interviewing process used in PROM development will be adapted in this study to test the Steroid PRO in new disease populations. Cognitive interviewing will be carried out using pragmatic, light-touch interviews, underpinned by think aloud techniques and clean language principles.

Sponsors

Johns Hopkins University
CollaboratorOTHER
University of Pittsburgh
CollaboratorOTHER
University of the West of England
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Aged ≥ 18 years old * Diagnosed with an autoimmune or inflammatory respiratory, gastroenterology or dermatology condition * Treatment with glucocorticoids with intravenous or oral glucocorticoids for an autoimmune or inflammatory condition within the previous year (or longer duration). * Ability to give consent.

Exclusion criteria

* Aged \<18 years old * No autoimmune or inflammatory respiratory, gastroenterology or dermatology diagnosis * Not treated with glucocorticoids with intravenous or oral glucocorticoids for an autoimmune or inflammatory condition within the previous year (or longer duration) * Unable to give consent

Design outcomes

Primary

MeasureTime frameDescription
Steroid PRONovember 2022 - May 2024Validated outcome measure to capture the impact of treatment with glucocorticoids on health related quality of life (Bridgewater ARD 2023). 15 item questionnaire, 4 domains (Impact on Appearance, Psychological Impact, Social impact and Treatment Concerns). Steroid PRO is the full title of the outcome measure. A PRO is a patient reported outcome. Higher scores equal greater impact on health related quality of life. Raw scores: minimum possible score 0, maximum 45.

Countries

United Kingdom

Contacts

Primary ContactJoanna C Robson, FRCP PhD
jo.robson@uwe.ac.uk0117 3427418
Backup ContactLeigh Taylor
leigh.taylor@uwe.ac.uk0117 328 1170

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026