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Your feedback is important to us. It will help us improve the quality of the study information on this site. Please answer both questions.
Contact the study team using the details below to take part. If there are no contact details below please ask your doctor in the first instance.
Matthew
Badura
ibho@bioresource.nihr.ac.uk
Natalie
Valle Guzman
ibho@bioresource.nihr.ac.uk
John
Bradley
john.bradley11@nhs.net
Miss
Hannah
Stark
ibho@bioresource.nihr.ac.uk
barbara
graves
ibho@bioresource.nihr.ac.uk
Vicky
Hills
vicky.hills@bioresource.nihr.ac.uk
Debbie
Clapham
debbie.clapham-riley@bioresource.nihr.ac.uk
More information about this study, what is involved and how to take part can be found on the study website.
Haemolytic anaemiasOther disorders of the skin and subcutaneous tissueMood [affective] disordersNeurotic, stress-related and somatoform disordersComplications of labour and deliveryComplications predominantly related to the puerperium
This information is provided directly by researchers, and we recognise that it isn't always easy to understand. We are working with researchers to improve the accessibility of this information. In some summaries, you may come across links to external websites. These websites will have more information to help you better understand the study.
The Improving Black Health Outcomes (IBHO) BioResource is focused on improving our knowledge and understanding of health conditions and their unique impacts on UK Black communities.
The UK lacks a dedicated research resource that can enable crucial studies to help us understand the health experiences of individuals from Black communities. The development of the IBHO BioResource will allow this important work with a view to better understanding and improved prognosis of common and rare health conditions in these communities. Participation contributes to shaping future healthcare strategies and interventions tailored to meet the needs of Black individuals.
We are inviting people aged 16+ from Black ethnic backgrounds, such as Black African, Black Caribbean and Black British to participate, whether they have a health condition or not. We are also inviting people with a confirmed diagnosis of Sickle Cell or Thalassaemia to join, regardless of ethnic background.
Children aged 15 and under with a confirmed diagnosis of Sickle Cell can also join the IBHO BioResource.
Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.
The recruitment start and end dates are as follows:
Observational type: Not Specified;
You can take part if:
You may not be able to take part if:
People who are not willing to be invited to future research projects. People who do not want their data and/or samples to be shared for research.
Below are the locations for where you can take part in the trial. Please note that not all sites may be open.
Matthew
Badura
ibho@bioresource.nihr.ac.uk
Natalie
Valle Guzman
ibho@bioresource.nihr.ac.uk
barbara
graves
ibho@bioresource.nihr.ac.uk
Vicky
Hills
vicky.hills@bioresource.nihr.ac.uk
John
Bradley
john.bradley11@nhs.net
Miss
Hannah
Stark
ibho@bioresource.nihr.ac.uk
Debbie
Clapham
debbie.clapham-riley@bioresource.nihr.ac.uk
More information about this study, what is involved and how to take part can be found on the study website.
The study is sponsored by CAMBRIDGE UNIVERSITY HOSPITALS NHS FOUNDATION TRUST and funded by NATIONAL INSTITUTE FOR HEALTH AND CARE RESEARCH .
Your feedback is important to us. It will help us improve the quality of the study information on this site. Please answer both questions.
Read full details
for Trial ID: CPMS 57264
You can print or share the study information with your GP/healthcare provider or contact the research team directly.
