Effect of Behavioral Intervention on Cannabinoid Receptors in BAD
NCT ID: NCT04168697
Last Updated: 2019-11-20
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
NA
20 participants
INTERVENTIONAL
2020-02-01
2021-02-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Stress Management in College Students
NCT05392621
Cannabidiol (CBD) and Stress Response: Psychobiological Mechanisms
NCT07069478
Effects of Hemp Oil on Markers of Optimal Wellness, Stress Resilience and Recovery in Healthy Subjects
NCT04294706
Evaluation of a Biofeedback-assisted Meditation Program as a Stress Management Tool for Hospital Nurses
NCT01011790
Mind Body Interventions for the Student Population
NCT03756701
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NON_RANDOMIZED
PARALLEL
BASIC_SCIENCE
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Controls
Control subjects undergoing an 8-week behavioral modification technique consisting of a combination of breathing exercises, cold exposure and meditation
Wim Hof method
8-week behavioral modification intervention instructing the participants in a combination of breathing exercises, cold exposure and meditation
BAD
Patients with bipolar affective disorder (BAD) undergoing an 8-week behavioral modification technique consisting of a combination of breathing exercises, cold exposure and meditation
Wim Hof method
8-week behavioral modification intervention instructing the participants in a combination of breathing exercises, cold exposure and meditation
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Wim Hof method
8-week behavioral modification intervention instructing the participants in a combination of breathing exercises, cold exposure and meditation
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Having experienced an acute affective episode in the past 3 years
* Having suffered at least two lifetime depressive episodes
* Monotherapy or combination with a mood stabilizer (lithium, valproate, carbamazepine or lamotrigine) at optimal doses, quetiapine monotherapy or in combination with the aforementioned stabilizers, any oral atypical antipsychotic in combination with an antidepressant
* Hamilton Depression Rating Scale (HDRS) score (\>8 and \<19) and Young Mania Rating Scale (YMRS) score \<10
* Being able to understand and agree with requirements of study protocol
Exclusion Criteria
* Any current DSM-IV diagnosis different from BAD (including substance or alcohol use disorder at the time of study entry, except if it is under complete remission. Not applicable to nicotine or caffeine)
* Risk of suicide or self/hetero aggressiveness
* Pregnancy
* Severe and unstable medical disease
* Mental retardation.
18 Years
65 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Wayne State University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Otto Muzik
Professor of Pediatrics
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Children's Hospital of Michigan
Detroit, Michigan, United States
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
19061167
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.