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Recruiting NCT07350395

NCT07350395 Exploring and Measuring the Impact of Steroids in Children and Young People

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Clinical Trial Summary
NCT ID NCT07350395
Status Recruiting
Phase
Sponsor University of the West of England
Condition Rheumatic Diseases
Study Type OBSERVATIONAL
Enrollment 70 participants
Start Date 2025-11-01
Primary Completion 2026-10-01

Eligibility & Interventions

Sex All sexes
Min Age N/A
Max Age 18 Years
Study Type OBSERVATIONAL

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 70 participants in total. It began in 2025-11-01 with a primary completion date of 2026-10-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Assessing the impact of glucocorticoids in children and young people with rheumatic conditions, to develop a patient reported outcome measure (PROM). Glucocorticoids, also known as steroids, are a very effective medication for the treatment of rheumatological conditions. They are used to reduce inflammation, pain and damage to organs. However, steroids can have some unwanted side effects, such as, increased weight, skin changes, feeling anxious, delayed puberty, diabetes and loss of bone mass. These side effects can therefore impact children and young people's health related quality of life (HRQoL). The investigators would like to create a new questionnaire for children and young people (CYP) who take steroids due to their rheumatological condition. The questionnaire, called a Patient Reported Outcome Measure, (PROM), will measure how steroids are affecting CYP. The first step in creating the questionnaire is to talk to children, young people and their parents/guardians about their experiences of taking steroids. The investigators plan to do this in focus groups, with people around the same age. The second step will then be to take everything people said in the focus group to create the questions in the questionnaire. Cognitive interviewing will then be used in a structured one on one interview to test for relevance, clarity and understanding of the questions. Children, young people and their parents/guardians will be involved throughout the research. Children and young people will give their thoughts and feedback on resources created for participants (consent forms/assent forms/participation information sheet/interview schedule), as well as how the focus groups and cognitive interviews should be structured. With consent, participants will be provided with a lay summary of the results. Results will also be published within peer-reviewed journals, special interest groups, trial meetings, patient charity meetings and presented at conferences.

Eligibility Criteria

Inclusion Criteria: * 1\. Rheumatology patients aged 0 to18 years old. 2. Patients should have capacity to assent or consent immediately prior to the interview. 3\. The patient should have a good understanding of spoken and written English be able to understand the participant information sheets, assent/consent forms. 4\. Treatment with glucocorticoids with intravenous or oral glucocorticoids for an autoimmune or inflammatory condition within the previous two years (or longer duration). Parents/guardians: 1. Parents (mother/ father) or legal guardians of rheumatological patients fulfilling criteria 1-4 above. 2. Parents or legal guardians should have capacity to consent for themselves (+/- their child) immediately prior to the interview. 3. The parents or legal guardians should have a good understanding of spoken and written English be able to understand the participant information sheets, assent/consent forms. Exclusion Criteria: * 1\. Rheumatology patients who are more than 18 years of age. 2. Patients who do not have capacity to assent or consent immediately prior to the interview. 3\. Patient who have insufficient understanding of spoken and written English be able to understand the participant information sheets, assent/consent forms. 4\. Patients who either have never taken steroids or have not taken steroids within the last two years as part of their treatment plan for their rheumatological condition. 5\. Relative is not a parent or legal guardian. 6. Parents/guardians of rheumatology patients fulfilling any of the exclusion criteria above. 7\. Parents/guardians who do not have capacity to assent or consent immediately prior to the interview. 8\. Parents/guardians who have insufficient understanding of spoken and written English be able to understand the participant information sheets, assent/consent forms. 9\. Parents/guardians of rheumatology patients who have never taken steroids or have not taken steroids within the last two years as part of their treatment plan for their rheumatological condition. 10\. Membership of the steering committee

Contact & Investigator

Central Contact

Emily Barnes

✉ emily4.barnes@live.uwe.ac.uk

📞 +447747560680

Frequently Asked Questions

Who can join the NCT07350395 clinical trial?

This trial is open to participants of all sexes, up to 18 Years, studying Rheumatic Diseases. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07350395 currently recruiting?

Yes, NCT07350395 is actively recruiting participants. Contact the research team at emily4.barnes@live.uwe.ac.uk for enrollment information.

Where is the NCT07350395 trial being conducted?

This trial is being conducted at Bristol, United Kingdom, Glasgow, United Kingdom, Liverpool, United Kingdom.

Who is sponsoring the NCT07350395 clinical trial?

NCT07350395 is sponsored by University of the West of England. The trial plans to enroll 70 participants.

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