Depression and Anxiety Trial, Recruiting
voxsanity.com.au · Eligibility summary from public government registries · 18 August 2026 · not medical advice
Who may and may not be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who may be able to join
- People who have been diagnosed with both ADHD and bipolar disorder (type I or II), with the bipolar disorder considered stable and in remission.
- People who have had no active depressive, manic, or psychotic episodes for at least 2 years.
- People who have not taken any psychiatric or brain-related medications — including mood stabilizers, antidepressants, antipsychotics, or ADHD medications — for at least 2 years.
- People who do not have any long-term physical health conditions, including neurological, heart, or metabolic disorders.
- People who have had a regular, consistent sleep and wake schedule during the week before the study.
- People who do not smoke.
- People who have not worked night shifts during the week before the study.
Who may not be able to join
Each point below is a reason the trial team may not be able to accept someone. It is not a list of requirements to meet.
- People who have an active or acute physical health condition that could affect how the study is carried out.
- People who have taken medications in the past 3 months that affect heart or brain function.
- People who have consumed alcohol or any mind-altering substances on the day before or the day of the study.
- People who have done intense physical exercise on the day before or the day of the study.
- People for whom moderate-intensity cycling exercise would not be medically appropriate — for example, due to a recent injury or an ongoing muscle or joint condition.
- People for whom an EEG brain activity recording would not be possible or appropriate — for example, due to a skin condition on the scalp that prevents proper electrode placement, or a sensitivity to the gels or pastes used during the procedure.
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Ida Laudańska-Krzemińska, Poznan University of Physical Education
Phone: (61) 835 53 49
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Mean EEG spectral power in theta, alpha, low beta, high beta, gamma frequency bands during resting-state (eyes-open and eyes-closed); Heart Rate Variability (HRV)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 17 August 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.