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: 2025-12-25 @ 2:51 AM
Ignite Modification Date: 2025-12-25 @ 2:51 AM
NCT ID: NCT07240233
Eligibility Criteria: Inclusion Criteria: * Adults receiving care at the university-affiliated dental clinic, legally able to consent and willing to participate voluntarily. * Ability to read and independently complete brief self-report questionnaires before and after the visit. Exclusion Criteria: * Self-reported hearing impairment, current use of hearing aids, or other auditory conditions that interfere with safe headphone use or outcome validity. * Use of sedative medication prior to the visit for the current appointment, or acute intoxication that may alter anxiety ratings. * Cognitive impairment or other condition that limits capacity to provide informed consent or to complete study questionnaires reliably. * Unwillingness to wear headphones during the procedure if randomized to a headphone arm, or refusal to participate/withdrawal of consent at any time. * Any urgent clinical indication that, in the clinician's judgment, precludes headphone use (for example, need for uninterrupted verbal interaction or imaging incompatible with wearing the device). * Reported history of severe adverse reactions to headphone use (for example, marked discomfort, vertigo) or skin sensitivity incompatible with device contact points. * Inability to protect privacy or comply with basic study procedures (for example, cannot complete pre- and post-visit questionnaires within the clinic workflow)
Healthy Volunteers: True
Sex: ALL
Minimum Age: 18 Years
Study: NCT07240233
Study Brief:
Protocol Section: NCT07240233