Cohort Studies
Overview
In this section you can find out about the experience of taking part in cohort studies by listening to people share their personal stories on film. Our researchers talked to 39 people from across the UK who had taken part (or decided not to take part) in cohort studies. Find out what people said about issues such as: the reasons they took part, what participation involved, and getting feedback from the studies. We hope you find the information helpful and reassuring.
You may also be interested in our other medical research and health and care research sections.
Taking part in cohort studies - site preview
Taking part in cohort studies - site preview
Gill
I think I’d say, “Go for it.” I mean it’s, it’s a, it’s not a difficult thing to do. It takes about, I suppose, half an hour or a bit longer to fill out the questionnaire and you just send it back. I mean, you know, it’s not hugely onerous from the point of view of time or effort, so I’d say go for it.
Even though they might not get any positive benefits that they can see?
Yes, yes well, it’s a philanthropic thing, isn’t it?
Ian
And every time they asked a question, they always made it quite clear that if it was something I was uncomfortable with, if I said, “No” it was never going to be a problem. And likewise, if I went ahead with anything and I wanted to stop it, it would never be a problem. It would never do any harm to my situation, and they would fully understand.
Eisha
Yeah, they talked about how do you, they talked about healthy eating, so there was a lot of questions regarding, ‘What do you eat?’ ‘How many meals?’ ‘How many fruit intake is in your diet?’ and then there were question regarding, ‘How do you feel?’ ‘How your moods?’ ‘Are you teary? Are you happy? So vaguely, I don’t remember clearly but I think those were the questions, yeah.
Anne
What’s been good is, recently, instead of a Christmas card that they sent us, they’ve actually sent out a sort of a newsletter which has had more information on it, so it’s making you feel more up to date. It’s also got a local Facebook page that I signed up to as well. There’s not many posts on it but, you know, people have been putting up photographs and things like that, yeah.
John
Well, if I can provide a data point in their research fantastic, just to be a data point is, is hopefully of use to them because the more people that they assess, the, the more understanding will emerge from that and the team is quite often in the broadsheet press, as it were, about recommendations and research findings. ‘Oh, that’s interesting. They’re still extremely active and our understanding of stroke/TIAs/the whole, you know, working of the brain is moving forward rapidly only because of research. So, if, if I’m a data point in that research that’s good news rather than my own experience being completely of no use to anybody, much better.
This section is from research by the University of Oxford.
Supported by
The research was funded by the National Institute for Health and Care Research (NIHR) Oxford Biomedical Research Centre (BRC). The views expressed are those of the author(s) and not necessarily those of the NHS, the NIHR or the Department of Health.
Publication date: August 2020.
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