Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-24 @ 2:49 PM
Ignite Modification Date: 2025-12-24 @ 2:49 PM
NCT ID: NCT06488859
Eligibility Criteria: Inclusion Criteria: * English-speaking * Low positive affect indexed by less than or equal to 24 on the positive affect subscale of the PANAS (i.e., PANAS-P); and scores of greater than or equal to 11 for depression and greater to or equal to 6 for anxiety on the Depression, Anxiety, and Stress Scale. * Score of greater than or equal to 4 on any WSAS subscale * Willingness to refrain from starting other psychosocial or pharmacological treatments until study completion. Exclusion Criteria: * Patient report of serious medical conditions - such as history of serious, uncontrolled medical illness, or instability (including significant cardio-pulmonary disease, organic brain syndrome, seizure disorder, cerebrovascular disease, thyroid dysfunction, and diabetes) * Current active suicidal ideation * Lifetime history of bipolar disorder, psychosis, cognitive impairment, or organic brain damage * Substance use disorder (including smoking) within the last 6 months. History of cocaine or stimulate use (e.g., amphetamine, cocaine, methamphetamine) * Greater than 11 cigarettes per week or nicotine equivalent * History of marijuana, cocaine or stimulant use 5-7 times/week or more before age 15 (e.g., amphetamine, cocaine, methamphetamine) * Willingness to refrain from marijuana use 1 week before laboratory assessments * Pregnancy * Bupropion, dopaminergic or neuroleptic medications use in the past 6 months * Heterocyclics and SSRIs are permitted if stabilized (3 months) and PRN benzodiazepines and beta-blockers are permitted but discouraged on laboratory assessment visits * Refusal of video/audio-taping * Prior participation in previous waves of this study
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Maximum Age: 65 Years
Study: NCT06488859
Study Brief:
Protocol Section: NCT06488859