NCT07676110 The Impact of Enhanced Music & Natural Visuals on Emotional Health
| NCT ID | NCT07676110 |
| Status | Recruiting |
| Phase | — |
| Sponsor | soundBrilliance LLC |
| Condition | Emotion Management Skills |
| Study Type | INTERVENTIONAL |
| Enrollment | 200 participants |
| Start Date | 2026-05-25 |
| Primary Completion | 2026-12 |
Eligibility & Interventions
Eligibility Fast-Check
Enter your details for a quick preliminary check. This does not replace medical advice.
What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 200 participants in total. It began in 2026-05-25 with a primary completion date of 2026-12.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
The investigators are conducting research on factors related to the self-regulation of mood and arousal states across a range of everyday activities as well as different levels of stress. Behavioral interventions-such as meditation, listening to music, or visualizing art or nature-offer important alternatives and/or adjunctive strategies to pharmaceutical tools or other mechanisms supporting physical and emotional well-being. This research will expand on the knowledge base regarding the impact of biophysical stimulation and/or frame of mind on an individual's self-directed management of physical and emotional health. Motivation, confidence, and composure are critical aspects of self-efficacy, framing a person's mindset to make healthy choices across daily activities. The research in this protocol is carried out across multiple sites and studies by means of digital tools and a consistent participant experience workflow. Together, these resources are intended to support individuals across multiple self-directed experiences utilized in the maintenance of their basic health. Before, during, and after session experiences, the participant provides objective (physiological) responses and/or subjective (self-report) responses and reflections; some studies also include interviews or focus groups. The combined set of responses can be summarized, connected to other measures, and input to machine learning models to improve personalization of stimuli. By studying the effects of soundBrilliance experiences across a variety of contexts and participant samples, the investigators can better refine each element of the stimulus to improve satisfaction, tolerance, and targeted outcomes.
Eligibility Criteria
Inclusion Criteria: * You are 13 years of age or older * You can read, write, and speak English at a 5th-grade level or higher * You are legally capable of providing informed consent (adult participants) or capable of providing assent (child participants) * To the best of your knowledge, you are willing and able to commit to the session(s) and activities of this study * You are willing and able to use the sound-delivery and data-collection apparatus of this study * You are willing to use your own personal equipment. Depending on the study, you may need to have your own ear buds/headphones and/or a "smart" device with internet and/or Bluetooth access (e.g., smartphone, iPad). * You have normal hearing in both ears. * You never experience ringing noises or buzzing sensations in your ears (tinnitus) * You do not use a heart/cardiac pacemaker and do not have any history of cardiac rhythm disturbances, such as cardiac conduction delays or blocks * You have no known history of fainting, fainting, spells or seizures, spinning sensations, or trouble with balance (medical terms include epilepsy, seizures, syncope, vertigo, nystagmus) * You do not use of any of the following medications: Beta blockers, steroids, ephedrine, acute anti-anxiety medication (e.g., benzodiazepines such as diazepam/Valium, lorazepam/Ativan or clonazepam/Klonopin), or acute or chronic pain medications (including narcotics and codeine) * For any study session, you will not be under the influence of any substances that could prevent safe participation and will not have consumed e.g., alcohol, THC, Psilocybin, or other mood-altering drugs in the 12 hours preceding the session. Exclusion Criteria: \-
Contact & Investigator
Robert Mele (VP of Clinical Research & Testing Operations), B.Eng
✉ rob.mele@soundBrilliance.com📞 7752444866
Jason S Doescher, MD
PRINCIPAL INVESTIGATOR
soundBrilliance LLC
Frequently Asked Questions
Who can join the NCT07676110 clinical trial?
This trial is open to participants of all sexes, aged 13 Years or older, studying Emotion Management Skills. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07676110 currently recruiting?
Yes, NCT07676110 is actively recruiting participants. Contact the research team at rob.mele@soundBrilliance.com for enrollment information.
Where is the NCT07676110 trial being conducted?
This trial is being conducted at Fort Collins, United States, Omaha, United States, Reno, United States.
Who is sponsoring the NCT07676110 clinical trial?
NCT07676110 is sponsored by soundBrilliance LLC. The principal investigator is Jason S Doescher, MD at soundBrilliance LLC. The trial plans to enroll 200 participants.