The LiPOC study is looking at whether lithium monitoring can be improved by using a quick finger-prick blood test that provides lithium results within minutes.

The study is comparing this point-of-care approach with usual lithium blood monitoring, to see whether it is practical and acceptable to people taking lithium for depression or bipolar disorder.

Who can take part?

We are looking for adults aged 18 or over who

  • have depression or bipolar disorder
  • are taking lithium
  • and are due to have their lithium monitored at least every three months

(The research study team will fully assess your eligibility.)

What does taking part involve?

You will be part of the study for about 30 weeks. You will go to three research appointments:

  1. at the start of the study
  2. around 15 weeks
  3. and around 30 weeks

You will complete questionnaires about your health, mood, lithium treatment and experiences of lithium monitoring. (These research appointments can take place remotely or in person.)

You will be randomly allocated to one of two groups.

One group continues with their usual lithium monitoring.

The other uses a quick finger-prick test that measures lithium levels in your blood, and provides results within minutes.

(You will be offered £20 for each research appointment, and up to £20 travel costs where applicable.)

Interested in taking part?

To find out more about LiPOC and whether you may be able to take part, please contact Research Assistant harry.brown@cntw.nhs.uk