Effect of Behavioral Intervention on Cannabinoid Receptors in BAD

NCT ID: NCT04168697

Last Updated: 2019-11-20

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-02-01

Study Completion Date

2021-02-01

Brief Summary

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The objective of this study is to determine whether the practice of a non-drug related intervention technique (behavioral modification technique consisting of a combination of breathing exercises, cold exposure and meditation) has an effect on long-term cannabinoid receptor function in a control group as well as in a group of patients suffering from bipolar affective disorder (BAD). Specifically, the objective of this study is to test whether the applied behavioral modification technique is able to alter cannabinoid receptor density in brain areas that modulate mood and motivational drive (such as vmPFC, PAG, VTA, amygdala and OFC). The investigators believe that these studies will form the impetus for a better understanding and deployment of non-drug related treatment methods in patients with various depressive symptoms. In particular, it appears that the proposed behavioral modification technique might be a powerful, currently under-appreciated, method to positively modulate the brain's own cannabinoid system.

Detailed Description

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Bipolar affective disorder (BAD) is often poorly controlled by prescribed drugs. Clinical observations suggest that the endocannabinoid system is dysfunctional in BAD and fails to control the level of cortical excitation and inhibition in the brain. Thus, excessively high endocannabinoid tone (mania) or excessively low endocannabinoid tone (depression) may manifest itself in BAD patients. Interestingly, cannabis use is common in patients with this disorder and anecdotal reports suggest that some patients take it to alleviate symptoms of both mania and depression. The investigators have recently studied brain activations during a cold stress paradigm in a 57 year old Dutch national (Wim Hof), the so-called "Iceman", who has the ability to withstand frequent prolonged periods of extreme cold exposure using a self-developed technique that includes a combination of breathing exercises, cold exposure and meditation (referred to as the WH technique). The WH technique allows the "Iceman" to regulate his own autonomic nervous system in the presence of severe cold and to perform remarkable acts of survival under extreme thermal conditions. Moreover, it has been shown that the WH technique can be successfully taught to novice users. Preliminary studies performed by the investigators have examined CNS mechanisms associated with the practice of the WH technique and the obtained findings unequivocally demonstrated activation of autonomic brainstem areas that are implicated in stress-induced analgesia as well as cognitive cortical areas that are associated with self-reflection (such as the anterior insula). In particular, a strong activation of the periaqueductal gray (PAG) was determined, which is implicated in the release of endogenous opiates/cannabinoids that mediate decreased sensitivity to cold exposure and (via connections to higher-order cortical areas) promote a feeling of euphoria and well-being. This finding suggests that the WH technique might allow practitioners to assert increased level of control over key components of the affective system and as a result might be a viable, non-drug related approach for patients with pathological mood swings. The investigators believe that this method might be particularly effective in patients suffering from BAD, as the practice of the WH technique can be implemented during both remission and at the onset of highly motivational manic episodes, which will then help to limit the effects of negative mood swings during depressive (and manic) episodes. The investigators will study the effects of the WH technique on cannabinoid receptor density using the cannabinoid PET tracer (F18-FMPEP-d2) by determining regional changes in cannabinoid receptor density in various brain regions prior and post behavioral intervention.

Conditions

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Bipolar Affective Disorder, Currently in Remission Bipolar Disorder I Bipolar Disorder II

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Patient group vs a control group
Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

NONE

no masking

Study Groups

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Controls

Control subjects undergoing an 8-week behavioral modification technique consisting of a combination of breathing exercises, cold exposure and meditation

Group Type EXPERIMENTAL

Wim Hof method

Intervention Type BEHAVIORAL

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

Group Type EXPERIMENTAL

Wim Hof method

Intervention Type BEHAVIORAL

8-week behavioral modification intervention instructing the participants in a combination of breathing exercises, cold exposure and meditation

Interventions

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Wim Hof method

8-week behavioral modification intervention instructing the participants in a combination of breathing exercises, cold exposure and meditation

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* BAD type I or II, in clinical remission of acute mood episode at least 3 months prior to study
* 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

* (i) Any acute mood episode in the 12 weeks before the start of the trial
* 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.
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Wayne State University

OTHER

Sponsor Role lead

Responsible Party

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Otto Muzik

Professor of Pediatrics

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Children's Hospital of Michigan

Detroit, Michigan, United States

Site Status

Countries

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United States

Central Contacts

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Otto Muzik

Role: CONTACT

3139932616

Vaibhav Diwadkar

Role: CONTACT

3135770164

Other Identifiers

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19061167

Identifier Type: -

Identifier Source: org_study_id

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