Paid Mental Health Clinical Trials in Austin

Inclusion Criteria:

• Has Generalized Anxiety Disorder as defined by DSM-5-TR
• If female is not pregnant or planning to become pregnant. If male is not planning to make a partner pregnant.
• Is willing and able to comply with the conditions and requirements of the study

Exclusion Criteria:

• Has a significant risk of suicide
• Has an active or medical history of bipolar disorder, schizophrenia, schizoaffective disorder, psychotic disorder and/or borderline personality disorder, or first-degree family history of psychosis or bipolar disorder
• Has other concurrent psychiatric disorders that is the primary disorder.
• Has other medically significant conditions rendering unsuitability for the study
• Has used or will need to use prohibited medications or therapies
• Has a known sensitivity or intolerance to study intervention or potential rescue medications

Inclusion Criteria:

• Has a primary diagnosis of fibromyalgia based on the 2016 ACR diagnostic criteria.
• Male or female, ≥18 years of age.
• Provides written informed consent to participate in the study before conducting any study procedures.

Exclusion Criteria:

• Previous participation in a clinical trial with reboxetine or esreboxetine or currently receiving treatment with reboxetine for any condition.
• Unable to comply with study procedures.
• Medically inappropriate for study participation in the opinion of the investigator.

• Access innovative study medications, study-related assessments, labs, and exams from board-certified clinicians—at no cost.
• Ages 18-65
• No cost to participate
• Studies typically compensate $100+ for each on-site visit. (range varies, ~$1000-1600 for full study completion)
• Travel reimbursement may be available. 
• Receive care from board-certified, psychiatrists and clinicians.
• Receive study-related lab evaluations and examinations.

• Access innovative study medications, study-related assessments, labs, and exams from board-certified clinicians—at no cost.
• Ages 18-65
• No cost to participate
• Studies typically compensate $100+ for each on-site visit. (range varies,  ~$1000-1600 for full study completion)
• Travel reimbursement may be available. 
• Receive care from board-certified, psychiatrists and clinicians.
• Receive study-related lab evaluations and examinations.

Access innovative study medications, study-related assessments, labs, and exams from board-certified clinicians—at no cost.

• Ages 18-74
• No cost to participate
• Studies typically compensate $100+ for each on-site visit. (range varies,  ~$1000-1600 for full study completion)
• Travel reimbursement may be available. 
• Receive care from board-certified, psychiatrists and clinicians.
• Receive study-related lab evaluations and examinations.

Inclusion Criteria:

• Primary diagnosis of BED according to DSM-5 criteria.
• Provides written informed consent to participate in the study before the conduct of any study procedures.
• Male or female, aged 18 to 55 inclusive.

Exclusion Criteria:

• Prior exposure to solriamfetol/Sunosi, through either a clinical study or prescription.
• Unable to comply with study procedures.
• Medically inappropriate for study participation in the opinion of the investigator.