Enrolling studies: Internet-Based Participation

Share on facebook
Share on twitter
Share on email

What: Researchers at Southern Connecticut State University are currently enrolling individuals in a study that will examine an intervention app for people living with ME/CFS. This app monitors daily perceived and expended energy and fatigue levels. Participants will be asked to complete an online survey about their health history, ME/CFS symptomology, as well as current perceived and expended energy and fatigue levels. Next, an online meeting will be established to review the app and participant opinions will be considered in future iterations of the intervention app.

Who: To qualify for this study, participants must have a ME/CFS diagnosis and read/speak English. A total of 20 individuals with and 20 individuals without ME/CFS will be recruited.

Where: Internet access is all that is required to participate in this study.

Additional Information: Participants can follow this link to the survey https://scsu.iad1.qualtrics.com/jfe/form/SV_6DtEvLJVUfYE0vP  or email Jemel at [email protected].

Share on facebook
Facebook
Share on twitter
Twitter
Share on whatsapp
WhatsApp
Share on google
Google+
Share on email
Email

4 thoughts on “Enrolling studies: Internet-Based Participation”

  1. Autumn Spires Smith

    I have ME/CFS. I live in SC. I’m 35 yrs old, female, Caucasian. I participated in one of Dr. jose Montoya’s research programs at Stanford University May of 2019. I live in SC USA. I speak English & I have internet access. I am interested in taking part if chosen.
    Thank You So Kindly!
    Autumn

  2. Do you know who the researchers are? I always am a bit leery of studies that don’t tell you who is doing it and don’t provide a link to the full study description

  3. I desperately need help with a diagnosis. Not one of my many doctors know anything about this illness, not even the rheumatologist i talked to. Her solution was the same as all the others….excercise therapy which I cannot handle.

Leave a Comment

Your email address will not be published. Required fields are marked *

Latest News

CDC website in browser tab

Sign on to #MEAction’s response to flawed CDC review

MEAction Response to CDC #MEAction has released a draft response to the CDC’s flawed systematic evidence review on ME/CFS treatments. Sign our form by August 15, 2021 to have your name added to #MEAction’s response before we formally submit it as a public comment on August 16. We need to demonstrate strong community opposition in

Read More »

Connecting Black People with ME and/or long Covid in the UK

Darren Randon, a poet, qualified teacher, community builder, facilitator, host and co-founder of Well Versed Ink from Thornton Heath, is launching a new group aimed at supporting Black and Black-mixed people with ME and/or long Covid in the UK. The group plans to create a safe space to share experiences and create community with the

Read More »

Help keep our work going

We rely on donations from people like you to keep fighting for equality for people with ME.

Donate

Get actions alerts and news direct to your inbox

You can choose what you want to be kept up to date on.

Subscribe
Scroll to Top