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= MDMA-assisted psychotherapy = From Wikipedia, the free encyclopedia Jump to navigationJump to search MDMA-assisted psychotherapy is the use of prescribed doses of MDMA as an adjunct to psychotherapy sessions. The study of MDMA as an enhancer for psychotherapy has been constrained since 1985 when the drug was classified in the United States as a Schedule I controlled substance. Research by the Multidisciplinary Association for Psychedelic Studies (MAPS) has provided evidence that MDMA can help address trauma-related disease, in particular post-traumatic stress disorder. In 2017, a Phase II clinical trial led to a designation of breakthrough therapy status by the US Food and Drug Administration (FDA).

The research is controversial due to the risks of taking MDMA, made evident by the illegal and unregulated use of MDMA in the form of ecstasy. There were 50 MDMA related deaths in the UK in 2014, and 10,000 hospitalizations for MDMA related illness/injury in 2011 in the US. The use of psychedelics for therapy has been characterized as 'countercultural' in Western cultures.

Contents

 * 1Post-traumatic stress disorder
 * 1.1Rationale for MDMA treatment
 * 1.2Procedure
 * 1.3Breakthrough therapy designation
 * 2Social anxiety disorder
 * 3Other research
 * 4Society and culture
 * 4.1Legality
 * 4.2Controversy
 * 5See also
 * 6References
 * 7External links

Post-traumatic stress disorder[edit]
Post-traumatic stress disorder (PTSD) is most commonly treated by cognitive behavioral therapy (particularly prolonged exposure and cognitive processing therapy), eye movement desensitization and reprocessing, and psychodynamic psychotherapy. However, over half of these patients continue to suffer from PTSD after completing therapy, with results from military PTSD being especially poor.

PTSD is best treated when a patient is in the ‘optimal arousal zone’. This is the zone in which emotions are engaged, yet not overwhelming. In this zone, the three key symptoms of PTSD are sedated. These are:

1.    Hyper-arousal: hyper-vigilance, insomnia, and aggression

2.    Intrusion: flashbacks and nightmares

3.    Avoidance: avoiding all trauma-related stimuli and social withdrawal

Subjects with PTSD exhibit extreme emotional numbing or anxiety and struggle to remain in the optimal arousal zone during conservative therapies. Threatening interpretations of memories are reinforced when patients are in low emotional states. If traumatic memories are revisited in therapy when a patient is not within the optimal arousal state, therapy for PTSD can actually increase the patient's trauma.

When used in therapy MDMA has been reported to increase empathy, closeness between patient and therapist, relaxation, motivation to engage with therapy and introspective thought, and to reduce depression and anxiety. MDMA makes it easier for a patient to stay in the optimal arousal zone by decreasing feelings of anxiety and defensiveness when revisiting traumatic memories. It also increases feelings of closeness and empathy, improving the patient's trust in the therapist, and encourages introspective thought to reassess memories and actions. These factors may increase the success rate of psychotherapy.

Side effects, which can last from a few hours to several days, include impaired balance, depression, fatigue, low mood, headache, nausea, loss of appetite, tightness and feeling cold.

Rationale for MDMA treatment[edit]
PTSD inhibits a subject’s ability to respond appropriately to trauma-related stimuli. The current model of PTSD proposes that it results from amplified and uncontrolled responses from the amygdala to trauma-specific cues. Treatment with MDMA has been shown to reduce blood flow to the amygdala, while increasing blood flow to the occipital cortex and ventromedial prefrontal cortex. This state reduces fear while enhances consciousness. MDMA also increases levels of the hormones serotonin, oxytocin, prolactin, and cortisol. Serotonin helps to regulate mood, while oxytocin has been found to increase trust and emotional awareness and reduce amygdala response. It has been proposed that these effects foster memory reconsolidation by allowing the patient to access the traumatic memory while feeling detached from the sense of imminent threat. MDMA reduces the activity of the amygdala

Procedure[edit]
In current studies of MDMA therapy a 125mg capsule of MDMA is orally administered. The subject is monitored, listens to emotionally provocative music, and engages in conversation with the therapist. After 2 hours, a supplemental 62.5mg dose of MDMA is administered orally. The therapist works with the patient for 6 hours, or until the psychedelic effects of the drug have worn off. Therapists encourage the patients to reach their own introspective conclusions, punctuated by discussion and collective reconsolidation of the memory. The patient stays in the clinic overnight to be monitored.

The following morning, the patient and therapist hold an integration session where they discuss the experimental session and process emotions. Three 90-minute integration sessions are held in the subsequent month. This process is repeated two or three times.

Breakthrough therapy designation[edit]
In 2017, the treatment was granted breakthrough therapy status by the FDA, a designation that indicates that there is preliminary evidence that an intervention offers a substantial improvement over other options for a serious health condition. In the Phase II trial, 61% of the 107 participants no longer qualified for PTSD two months after they underwent three sessions of MDMA-assisted psychotherapy, according to MAPS. The participants had all suffered from chronic, treatment-resistant PTSD for an average of 17.8 years. MAPS and the FDA have agreed on the design for the Phase III trial, and if the trial is successful the treatment could be approved as early as 2021.

In trials, the drug has been administered solely in clinics designed for MDMA psychotherapy. If the drug is approved, decisions will need to be made on what qualifications physicians will need in order to prescribe and administer the drug, and how the drug will be produced and stored.

Currently MDMA is being looked at for the treatment of other diseases. Things like anxiety related to life threatening diseases, and other psychological diseases.

Social anxiety disorder[edit]
Researchers at the Los Angeles BioMedical Research Institute reported a study of MDMA-assisted psychotherapy for autistic adults with social anxiety disorder in 2018. The goal of the study was to explore the feasibility of treating the patients' social anxiety with MDMA-assisted therapy, rather than to reduce atypical responses associated with autism. The study used the same procedure as the MDMA-assisted psychotherapy treatment for PTSD. The study also included mindfulness therapies, and was held in a room that included natural elements (e.g. fresh flowers), fidget objects, and other items that are helpful for many autistic adults. Enrollment in the study was contingent on a score of more than 60 on the Liebowitz social anxiety scale - a score that indicates 'difficulties functioning socially and distress'.This study compared the MDMA group with a placebo group. The MDMA group's reduction in anxiety was considerably greater than that for the placebo group, and was retained at 6-month follow up sessions. Side effects of anxiety, difficulty in concentrating, headache, fatigue and depression were noted, however.

Alcohol Use Disorder
There is currently an ongoing study at Bristol Imperial that is using MDMA assisted psychotherapy for people dealing with Alcohol Use Disorder. The study will have two MDMA assisted psychotherapy sessions for the estimated 20 participants. The participants in the study will be given 125mg of MDMA and be offered an additional dose of 62.5mg 2 hours later. The participants in the clinical trial are patients with alcohol use disorder post-detoxification. The study's estimated date of completion is June 12, 2020, but there have not been any updates on the results of the study.

Other research[edit]
MDMA has been proposed as an adjunct for other psychiatric disorders. For example, MDMA-assisted psychotherapy has been tested in a pilot study of anxiety related to advanced stage cancer. This study was terminated due to lack of funding and insufficient patient enrollment. Recreational users have published personal testimonies recounting positive body image experiences both during and following their use of MDMA, and MDMA-assisted psychotherapy has been proposed as a potential treatment for eating disorders. MDMA molecular structure

Legality[edit]
MDMA was first synthesized by German pharmaceutical company Merck KGaA in the early 1900s as an intermediate in the synthesis of another compound. Its psychedelic effects were not noted until the early 1960s. In the 1960s and 1970s, the drug was used in psychotherapy, although it was not an approved drug and no clinical trials had been performed. The drug was studied in Switzerland for use in individual, couple, and group therapies until 1993.

In 1985, MDMA was given Schedule I status in the United States due to its high potential for abuse, and most research was stopped. Researchers interested in MDMA for use in psychotherapy founded and funded the Multidisciplinary Association for Psychedelic Studies (MAPS) in response. The US Food and Drug Administration (FDA) and Drug Enforcement Administration (DEA) granted approval for researching MDMA’s efficacy as an adjunct to psychotherapy in 2004, and the first trial was carried out in 2011. Recently in January of 2020, the FDA approved a MAPS request for an Extended Access Program for MDMA-assisted psychotherapy for people with PTSD. ☃☃☃☃

In society the drug has been looked at as a rave drug. Something for concert goers, ravers, and people just looking for a good time. As research has devolved it seems the drug can also be good for crippling psychological diseases.

Controversy[edit]
MDMA is unpredictable and produces different responses in different people. The drug causes neurotransmitter activation across the main neural pathways (including serotonin and dopamine, noradrenaline) that can result in large mood swings and changes. The memories that emerge under the influence of MDMA can evoke unwanted emotions. Side effects of MDMA use by recreational users include appetite fluctuations, food cravings, and disordered eating.

Once the effects of MDMA wear off, there is a "period of neurochemical depletion" that invokes anhedonia, lethargy, anger, depression, irritability, brooding, greater everyday stress, altered pain thresholds, changes in sleep, and bad dreams, especially in female participants. The symptoms are thought to be due to depletion of serotonin, as a result of the large release of serotonin triggered by MDMA, and have been called "neurotoxic in terms of causing serotonergic dysfunction".

There are also concerns surrounding "drug-dependent learning" — the theory that patients will return to the drug to access the state they were in when on the drug in therapy. However, MDMA is described as a “self-limiting” drug as the intensity of the positive effects decreases with increased use, while negative effects increase. Dependency rates are low compared to other illicit drugs, at 1% of users.

See also[edit]
''I didn't see an article evaluated in your sandbox. If you decide to complete this assignment for partial credit - please let me know. --Liz''