RECRUITING

BTL-699-2 for the Improvement of Sleep Quality and Reduction of Stress

Description

The goal of this clinical trial is to evaluate whether the treatment with BTL-699-2 device is able to improve sleep quality and reduce stress in adults above the age of 22 years. The main questions it aims to answer are: Does the treatment with BTL-699-2 device improve sleep quality? Does the treatment with BTL-699-2 device reduce stress? Participants will be asked to: * Undergo six treatments * Complete the Pittsburgh Sleep Quality Index * Complete the Perceived Stress Scale Questionnaire * Complete the Sleep and Stress Assessment Questionnaire * Complete the Therapy Comfort and Subject Satisfaction Questionnaire

Study Overview

Study Details

Study overview

The goal of this clinical trial is to evaluate whether the treatment with BTL-699-2 device is able to improve sleep quality and reduce stress in adults above the age of 22 years. The main questions it aims to answer are: Does the treatment with BTL-699-2 device improve sleep quality? Does the treatment with BTL-699-2 device reduce stress? Participants will be asked to: * Undergo six treatments * Complete the Pittsburgh Sleep Quality Index * Complete the Perceived Stress Scale Questionnaire * Complete the Sleep and Stress Assessment Questionnaire * Complete the Therapy Comfort and Subject Satisfaction Questionnaire

Safety and Efficacy of BTL-699-2 for the Improvement of Sleep Quality and Reduction of Stress

BTL-699-2 for the Improvement of Sleep Quality and Reduction of Stress

Condition
Sleep Quality
Intervention / Treatment

-

Contacts and Locations

Chula Vista

AntiAging and Wellness, Chula Vista, California, United States, 91914

Encinitas

Kind Health Group, Encinitas, California, United States, 92024

Minooka

Minooka Healthcare Center, Minooka, Illinois, United States, 60447

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Age \> 22 years
  • * The minimal pre-treatment PSQI score of \>= 5 points
  • * Ability to determine the motor threshold of the participant. The participant's motor threshold could be established as the minimum stimulus required to induce contraction of the right thumb
  • * Subjects willing and able to abstain from partaking in any treatments other than the study procedure for the improvement in sleep quality and reduction of stress, including non-invasive brain stimulation treatments other than the study procedure during study participation
  • * Subjects willing and able to maintain their regular (pre-procedure) diet and exercise regimen without affecting significant change in either direction during study participation
  • * Willingness to comply with study instructions and to return to the clinic for the required visits
  • * Women of child-bearing potential\* are required to use birth control measures during the whole duration of the study
  • * If applicable, subjects will be maintained on pre-study prescribed medications at a stable therapeutic dosage for at least 2 months prior to study entry
  • * Subject is not using any sleeping medication or is using over-the-counter pills (except Valerian and St. John's Wort) no more than 4 times a week
  • * Electronic implants in or near the head - rTMS devices are contraindicated for use in patients who have active or inactive implants in or near the head including device leads, deep brain stimulators, cochlear implants, ocular implants, and vagus nerve stimulators, implanted devices such as cardiac pacemakers, defibrillators, and neurostimulators
  • * Metallic, ferromagnetic or other magnetic-sensitive implants/objects in or near the head - rTMS devices are contraindicated for use in patients who have conductive, ferromagnetic or other magnetic-sensitive metals implanted in their head (with some exceptions in the mouth - see Operator's Manual) or within 12 in (30 cm) of the therapy coil. (Examples include implanted electrodes/stimulators, aneurysm clips or coils, stents, bullet fragments, jewelry, hair barrettes and tattoos with metallic ink),
  • * Drug pumps (within 12 in (30 cm) of the therapy coil)
  • * Application in the heart area
  • * Persons with a tendency to seizure (hypotonic, epileptic)
  • * Ongoing anticoagulation therapy
  • * Ongoing severe or life-threatening condition
  • * Pulmonary insufficiency
  • * Heart disorders
  • * Renal insufficiency
  • * Decompensated\* hemorrhagic conditions, blood coagulation disorders, cardiovascular diseases
  • * Malignant tumor, benign tumor
  • * Fever
  • * Ongoing pregnancy
  • * Suicidal tendencies or recent attempt to commit suicide
  • * Concurrent use of electroconvulsive therapy or vagus nerve stimulation
  • * Substance-induced depression or depression secondary to a general medical condition
  • * Seasonal affective disorder
  • * Substance abuse, obsessive compulsive disorder or post-traumatic stress disorder, major depression
  • * Psychotic disorder including schizoaffective disorder, bipolar disease or major depression with psychotic features
  • * Neurological disorders, including a history of seizures, cerebrovascular disease, primary or secondary tumors in CNS, cerebral aneurysm, dementia or movement disorders
  • * History of increased intracranial pressure or head trauma
  • * Nursing
  • * Usage of prescription sleep medication, Valerian of St. John's Wort in the past 2 months
  • * Usage of over-the-counter pills 5 or more times a week

Ages Eligible for Study

22 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

Yes

Collaborators and Investigators

BTL Industries Ltd.,

Study Record Dates

2026-08-02