Clinical trials in plymouth

If you need help with an existing study, please ensure you have sufficient funds to meet the costs of our support. At PenCTU we support the development and delivery of clinical and applied health and care research. We offer a range of services, from pre-application methodological support to full study delivery. PenCTU has expertise in designing, developing, supporting and co-ordinating high quality research studies to applicable standards and regulations — working with us.

We have expertise in pilot trials and feasibility studies, longitudinal cohort studies, drug trials, other non-drug interventional trials, trials of complex interventions, across a broad range of clinical and health and care related areas. Ask as many questions as you need to and discuss it with friends and family before making your decision. If you decide to go ahead, you will normally need to sign a consent form to confirm that you wish to be involved. Remember that you are not obliged to take part in any research.

If you decide that you would rather not take part, this will not affect your care. If you decide to take part but subsequently decide you no longer wish to continue, you can leave the study at any time. Whilst it is something we hope will not happen, if you have concerns about any aspect of research please speak to the researchers using the contact details you will have been provided with. Short term commitment including four, 1-hour meetings.

Participants are compensated for their time. Caregivers, we are inviting you to join a fitness study to find the best ways to help caregivers increase physical activity. This study is looking at the effects of pet dogs on stress in older adults and their in-home family caregivers. Participation includes a one-time, approximately two-hour session completed at home where participants older adults and their caregivers will fill out surveys on their stress level and quality of life.

The survey takes approximately 10 minutes to complete and includes questions about how you have felt during the pandemic and your experiences of accessing support, including how this has been impacted …. The goal of the study is to see if a group, in-person dementia caregiver education and support program can be successfully done virtually, that is, by using a laptop or tablet connected to the internet. If successful, that would mean that caregivers could attend these groups either from their home ….

It will be protected with a passcode Generate session link. Access your activity on CenterWatch with a private link and passcode. Share Passcode: Copy to clipboard. Plymouth, Indiana Clinical Trials A listing of Plymouth, Indiana clinical trials actively recruiting patient volunteers.

Please select a valid location from the dropdown. We often hear of the inspirational stories of those who participate in clinical trials, fighting for future generations and improving their quality of life. However, we know little of the people who see the patients every day, those who work to maintain a safe environment.

Re:Cognition Health in Plymouth describes the different roles in a clinical trial and gives their insight into what it means to them to work in this field. First, there is the Principal investigator. The principal investigator is responsible for everything that goes on in the department.

Their priority is the health and safety of the patients. They are the point of contact for the patients at any time. They are also responsible for the reliability of the data to ensure that the outcomes are valid and show that the new medicine is safe as well as effective. Working alongside the principal investigator is the Sub-investigator , whose role is to ensure the safety of the patients with the utmost care, respect, and professionalism.

They inform about the processes of a trial at the start, talking about cognitive decline and whether they think a patient may have it, as well as ensuring safety throughout the trial. This role is held by Dr Vicky Evans. To ensure the day-to-day running of the clinic there are the Study coordinators who liaise with all relevant staff members, agencies, and departments, maintaining documentation, preparing the study drug, stock control of study and non-study materials and the welfare of patients.

This role is held by Hannah Palmer and Sarah Legg.