Hello, a study being conducted through Hofstra University is currently seeking participants. The purpose of this study is to further our understanding of the use of online social networking tools among people experiencing social anhedonia. This is a symptom commonly seen in disorders like schizophrenia, wherein a person reports taking little or no pleasure from interacting with others.
Participation in this study is estimated to take one hour. In exchange for your time, you will be entered into a drawing for one of three gift cards to Amazon.com valued at $100.00. You will also be contributing to a greater body of knowledge concerning the behavior of individuals with social anhedonia and their utilization of social networking services.
In order to be eligible to participate, you must meet the following requirements:
You must have been previously diagnosed with schizophrenia or schizoaffective disorder by a psychiatrist or psychologist.
You must be between the ages of 18 and 65.
You must be a resident of the United States and fluent in English.
Does it ask for personally identifiable information - like your name? I think these types of things are typically anonymous - so you don’t need to worry about anonymity.
I encourage people to participate to help move research forward.
Hi everyone! The reason that I ask for name and contact info is in case you win the drawing. Other than that, I don’t really have any need for it, so you can give false info if you want. Otherwise, I keep all the information I collect confidential and the identifying parts will be destroyed after the drawing is over.
Thanks for your interest, let me know if you have any other questions and I’ll be happy to answer!
HI everyone, I’m just posting to give this a bump. I’m still looking for a few more participants, so if anyone is willing to give me a hand, I’d greatly appreciate it.
There were some concerns before about giving your name, but I’ve been told it’s OK to remove that question, so I have. Let me know if you have any other questions or concerns!
Unfortunately, yes. I’m also collecting data at the hospital where I work, so in order to keep the sample somewhat consistent, I have to limit participation to people who live in the US.
I refuse to fill out surveys asking for info that personally identifies me. 99% of the stuff asking for this online is bad news. If there was a version that didn’t request this, sure, but I’m not going anywhere near it in its current form.
I wish that I could, but there isn’t really any way that’s both practical and ethical to have people sharing that information with me. So, I have to rely on people being honest about their diagnosis.