Phase
Condition
Insomnia
Sleep Disorders
Treatment
Neurofeedback
Clinical Study ID
Ages 18-35 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Male or female aged between 18 and 35 years old,
Healthy subject, no pathology reported at the interview
Absence of EDS complaints (total ESS score<11) and sleep complaints (total InsomniaSeverity Indexscore <15)
Presence of an objective EDS measured by a mean sleep latency of less than 30minutes on the wakefulness maintenance test performed after a night of total sleepdeprivation under controlled conditions (at the inclusion visit),
Motivated to carry out the program of 8 neurofeedback sessions,
Body mass index < 25 kg/m2,
Affiliated with the social security (beneficiary or entitled person),
Having been informed and having signed an informed consent.
Exclusion
Exclusion Criteria:
All pathologies that may induce excessive daytime sleepiness: untreated narcolepsyor idiopathic hypersomnia, untreated sleep apnea syndrome, untreated restless legssyndrome, untreated periodic leg movement syndrome, unstabilized psychiatricdisorders of the characterized depressive disorder type, anxiety disorders, bipolardisorder, addictive disorders (alcohol and drugs), obesity having undergone surgicaltreatment for less than 3 months.
Chronic insomnia disorder
Excessive consumption of coffee, tea, or caffeinated cola type beverages (> 5cups/day)
All pathologies making interaction with the neurofeedback device potentiallyproblematic: intellectual, visual, auditory or motor impairment, psychoticdisorders, unstable cardio-respiratory diseases, neurological disease of the centralnervous system, confusion, dementia,
Any situation or treatment modifying the EEG spectral power: psychotropictreatments, night or shift work, chrono-biological disorders interfering with thelevel of daytime alertness, history of cranial surgery, epilepsy,
Pregnant or breastfeeding woman,
Persons placed under the safeguard of justice,
A person participating in another research study with an exclusion period still inprogress,
Person whose physical and/or psychological health is severely impaired
Study Design
Study Description
Connect with a study center
CHU de Bordeaux
Bordeaux, 33000
FranceSite Not Available

Not the study for you?
Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.