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Why it’s worth participating in research

1. Direct rewards

Sometimes, taking part in research has a direct benefit to the participant. This can be in the form of monetary reimbursement or a token of thanks from the researchers. This is usually true of smaller studies that take up a lot of time, or that involve an activity that some people would find unpleasant. Benefits can come in many different forms depending on the type of research carried out. Participants taking part in brain imaging studies may be offered a picture of their brain, or those trialing a new online treatment may receive a free course.

More often, larger scale studies aiming to recruit hundreds or thousands of participants are unable to reimburse every participant directly. These studies, such as EDGI, instead aim to reduce the input needed from participants, for example through making questionnaires accessible on mobile phones so that they can be completed on-the-go and sending out saliva kits to be completed at home.

“Participants know that they have contributed towards knowledge about mental health that may help others in the future”

2. Helping scientific research

These types of study can be seen as having no immediate benefit to the participant, although many people still find it very rewarding. Participants know that they have contributed towards knowledge about mental health that may help others in the future, be it through understanding the causes of an illness, informing treatment development or helping to reduce stigma about a certain condition. It can be incredibly fulfilling to know that your participation has helped progress in science. Many researchers will update participants about the findings from their study, or will inform participants of any papers that result from the research when they are published. This way, participants are made aware of exactly how their contribution has added to knowledge and helped others.

3. Becoming part of a community

Taking part in a large scale study also offer participants the opportunity to be part of a community of people interested in mental health research. One of the aims of EDGI is to create a community of researchers and participants who are able to help each other. Members are provided with a resource of information about mental health difficulties, treatments and where to seek help if it is needed, and are able to opt in to the research projects that interest them. Rather than making a one-off contribution, participants are a part of the bigger picture of mental health research and of EDGI community.

“Rather than making a one-off contribution, participants are a part of the bigger picture of mental health research”

4. Learning and reflecting

Finally, many participants describe taking part in research as a way for something good to come out of their struggles. Being able to reflect on their experiences and use that information to help others in the future can be seen as a positive outcome to a difficult time. Overall, every participant has their own reasons for wanting to get involved in research, whether to directly gain something, to know that they have helped others or to turn their own experiences into something positive. It is these participants who have made advances in the field of mental health research possible.

“It is these participants who have made advances in the field of mental health research possible.”

Date:June 21, 2021
Authors: Alicia Peel, Rosa Cheesman
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Am I Eligible?

To take part in the GLAD Study you must either:

  • Have ever experienced anxiety or depressive disorders (with or without a medical diagnosis)
  • Have never experienced any mental health disorder.

AND you must:

  • Be aged 16 or over
  • Live in the United Kingdom

Sign up to the GLAD Study

The Genetic Links to Anxiety and Depression (GLAD) Study is currently only recruiting individuals over the age of 16. If you are younger than 16, unfortunately you are not eligible for the GLAD Study.

You can withdraw from the study at any time.

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After completing the sign-up form, the study enrollment process consists of the following four steps:

  • Reading the Information Sheet
  • Providing consent
  • Completing our questionnaire
  • Providing a saliva sample
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