Recover SLEEP
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StatusAccepting Candidates
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Age18 Years - 75 Years
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SexesAll
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Healthy Volunteers
Description
Researchers are studying possible treatments for adults who have Long COVID, which is when a person has symptoms months after getting COVID. Symptoms can include trouble breathing, a cough, trouble sleeping, feeling weak and tired, and problems with certain organs, such as the heart or kidneys. We want to enroll adults from many different backgrounds in this clinical trial to learn if study drugs, devices, or other approaches may work to improve sleep quality, daytime tiredness, or excessive sleepiness in people who have long COVID.
Details
Protocol number | CED000000937 |
Eligibility
You may be a good fit for this study if:
You are an adult who had COVID You do not have an active COVID infectio
You still have 1 or more of these symptoms:
Problems falling asleep or staying asleep Poor sleep quality Trouble staying awake or feeling very tired during the day Insomnia or problems with your sleep-wake schedule
You are not pregnant or breastfeeding
Lead researcher
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Carmen Isache, MDInternal Medicine Physician (Internist), Infectious Disease Physician
Participate in a study
Here are some general steps to consider when participating in a research study:
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Step1
Contact the research team
Call or email the research team listed within the specific clinical trial or study to let them know that you're interested. A member of the research team, such as the researcher or study coordinator, will be available to tell you more about the study and to answer any questions or concerns you may have.
Primary contact
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Step2
Get screened to confirm eligibility
You may be asked to take part in prescreening to make sure you are eligible for a study. The prescreening process ensures it is safe for you to participate. During the prescreening process, you will be asked some questions and you may also be asked to schedule tests or procedures to confirm your eligibility.
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Step3
Provide your consent to participate
If you are eligible and want to join the clinical trial or study, a member of the research team will ask for your consent to participate. To give consent, you will be asked to read and sign a consent form for the study. This consent form explains the study's purpose, procedures, risks, benefits and provides other important information, such as the study team's contact information.
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Step4
Participate
If you decide to participate in a clinical trial or study, the research team will keep you informed of the study requirements and what you will need to do to throughout the study. For some trials or studies, your health care provider may work with the research team to ensure there are no conflicts with other medications or treatments.