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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.

Contact Information:

Emma Webb
emma.webb@nnuh.nhs.uk


Emma Webb
emma.webb@nnuh.nhs.uk


Study Location:

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Be Part of Research - Trial Details - VITASCOPE

VITASCOPE

Completed

Open to: Female / Male

Age: 10 Years - N/A

Medical Conditions

Obesity and other hyperalimentation
Other nutritional deficiencies


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.


Childhood obesity is a global health crisis with 1.2 million children in England severely obese, predisposing them to multiple health risks which decrease lifespan and compromise health. Children suffering from obesity experience a state of paradoxical malnutrition; despite excessive calorie intake they have high rates of micronutrient deficiencies rates due to consumption of energy dense, nutrient poor diets. Around 70-80% of obese children are Vitamin D deficient, 10% have low B12 concentrations and 50% have folic acid deficiency.
Currently screening for micronutrient deficiencies does not form a routine part of clinical care at all medical centres because they require a large volume of blood and are expensive to perform. We have developed a prototype point-of-care in-vitro diagnostic test which allows at-home/primary care testing of micronutrient levels, using an integrated finger-prick and minimal amount of blood. This device should be simple to use, with just one push of a button. The results are analysed using a phone app for clear decision-making, with data uploaded to healthcare providers automatically.

This study aims to ask service users (young people and their families) for their views on the usability and acceptability of the device prior to developing the product further.

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:

25 Jun 2024 27 Sep 2024

Observational

Observational type: Cohort study;



You can take part if:



You may not be able to take part if:


Potential participants will not be eligible if they lack capacity to provide informed consent (or in the case of young people under the age of 16, informed assent and informed parental consent).


Below are the locations for where you can take part in the trial. Please note that not all sites may be open.


The study is sponsored by NORFOLK AND NORWICH UNIVERSITY HOSPITALS NHS FOUNDATION TRUST and funded by NHS ENGLAND .




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for Trial ID: CPMS 62431

Last updated 09 July 2025

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