| Literature DB >> 35756295 |
Mauro Cavarra1,2, Alessandra Falzone1, Johannes G Ramaekers2, Kim P C Kuypers2, Carmela Mento3.
Abstract
Modern clinical research on psychedelics is generating interesting outcomes in a wide array of clinical conditions when psychedelic-assisted psychotherapy is delivered to appropriately screened participants and in controlled settings. Still, a number of patients relapse or are less responsive to such treatments. Individual and contextual factors (i.e., set and setting) seem to play a role in shaping the psychedelic experience and in determining clinical outcomes. These findings, coupled with data from literature on the effectiveness of psychotherapy, frame the therapeutic context as a potential moderator of clinical efficacy, highlighting the need to investigate how to functionally employ environmental and relational factors. In this review, we performed a structured search through two databases (i.e., PubMed/Medline and Scopus) to identify records of clinical studies on psychedelics which used and described a structured associated psychotherapeutic intervention. The aim is to construct a picture of what models of psychedelic-assisted psychotherapy are currently adopted in clinical research and to report on their clinical outcomes. Ad-hoc and adapted therapeutic methods were identified. Common principles, points of divergence and future directions are highlighted and discussed with special attention toward therapeutic stance, degree of directiveness and the potential suggestive effects of information provided to patients.Entities:
Keywords: psychedelic-assisted psychotherapy; psychedelics; review; set and setting; theoretical models
Year: 2022 PMID: 35756295 PMCID: PMC9226617 DOI: 10.3389/fpsyg.2022.887255
Source DB: PubMed Journal: Front Psychol ISSN: 1664-1078
Figure 1PRISMA flowchart.
Summary of included studies.
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| Wagner et al. ( | 6 couples | Pre-post | 2, MDMA (75, 100 mg) | CBCT | None | End of treatment and 6-month follow up | CAPS-5, PCL-5, CSI | Improved symptomatology and couple satisfaction |
| Wilkinson et al. ( | 40, TRD | RCT | 28 responders to previous course of 6 ketamine infusion sessions (0.5 mg/kg) randomized to either CBT ( | CBT | TAU | 14 weeks after last infusion | MÅDRS, QIDS | Significantly lower QIDS in CBT group. Significantly lower MÅDRS for the whole sample. |
| Ocker et al. ( | 1, opioid addiction | Case study | 5-day ketamine infusion (10 mg/h,0.09 mg/kg/h−70 mg/h, 0.6 mg/ kg/h) | CBT | None | 30-day follow up | NRS, opioid use | Pain-free and no reported opioid use |
| Wilkinson et al. ( | 16, TRD | Open-label | 4, ketamine (0.5 mg/kg) | CBT | None | End of treatment and 12 weeks after last ketamine session | MÅDRS, relapse rate | Most relapses occurred after the completion of the CBT course. Ketamine non-responders did not seem to benefit from CBT. |
| Johnson et al. ( | 12, tobacco addiction | Open-label | 2 or 3, psilocybin (20 mg/70 kg, 30 mg/70 kg) | CBT for smoking cessation | None | 6-month follow up, 12-month follow up | Biomarkers of smoking status and self-report measures of smoking behavior | 80 and 67% abstinence |
| Bowen et al. ( | 81, AUD; 59, AUD | Open-label clinical trial | 1, LSD (500 or 25 μg) | HRTL | No drug or “low” dose. | 1 year after end of treatment | Custom adjustment level measure | No significant differences. |
| Kolp et al. ( | ~70, AUD | Case series | 1 or 2 | KEP | None | 1 year | Abstinence rates | 25–70% |
| Kolp et al. ( | 2, LTI | Case study | 1 (150 mg i.m.) | KET | None | End of life | Qualitative reports | Case 1: remission from panic attacks, relief from pain, discontinuation of painkillers. Case 2: no reported improvements. |
| Krupitsky et al. ( | 59, heroin addiction | RCT, single vs. repeated ketamine doses | 1 or 3, Ketamine (2.0 mg/kg im) | KPT | Single ketamine dose | 1-year follow up | Abstinence rates | Greater abstinence rate in the repeated dose group |
| Krupitsky et al. ( | 70, heroin addiction | RCT | 1, ketamine (2.0 mg/kg im) | KPT | Ketamine, low dose (0.20 mg/kg im) | 2-year follow up | Abstinence rates, Craving VAS | Greater abstinence rate and lower craving scores |
| Krupitsky and Grinenko ( | 111, AUD | Non-randomized controlled trial | 1, ketamine (2.5 mg/kg, im) | KPT | TAU | 1-year follow up | Abstinence rate | Greater abstinence rate |
| Ross et al. ( | 29, life-threatening cancer | RCT | 1, psilocybin (0.3 mg/kg, p.o.) | MAP | Niacin | 7, 6.5, 4.2 years | HADS, BDI, STAI | Improved depression and anxiety scores |
| Pahnke et al. ( | 31, life-threatening cancer | Pre-post | 1, LSD (200–500 μg) | MAP | None | End of treatment | Custom rating scale filled by external observers (e.g., relatives, clinical staff) | Improved scores of emotional and physical distress |
| Kurland ( | 4, life-threatening cancer | Case series | 1–4, LSD (100–400 μg) | MAP | None | End of treatment | Unstructured clinical evaluation | Improvement in mood, optimism and pain management |
| Danforth et al. ( | 12, autistic adults | RCT | 2, MDMA (75–125 mg) | MDMA-assisted therapy and mindfulness for adult autistic individuals | Inactive placebo | 6-month follow up | LSAS | Improvements in social anxiety |
| Jardim et al. ( | 3, PTSD | Case series | 3, MDMA (75, 75, 125 mg) | MDMAAP | None | 2 months after treatment | CAPS-4 | Improvements in symptoms, depression Clinically significant CAPS score reductions; improvements in BDI, PTGI and GAF |
| Mithoefer et al. ( | 105 (pooled), PTSD | RCT | 2, MDMA (75–125 mg) | MDMAAP | Inactive placebo or active control (40 mg MDMA) | End of treatment, 12-month follow-up (minimum) | CAPS-4 | Improvements in CAPS-4 scores between baseline and end of treatment and between end of treatment and follow up |
| Bouso et al. ( | 6, PTSD | RCT | 1, MDMA (50 or 75 mg) | MDMAAP | Inactive placebo | End of treatment | SSSPTSD, STAI, BDI, HAM-D, MSF, MS, SE/R | Reduced symptomatology |
| Mitchell et al. ( | 90, PTSD | RCT | 3, MDMA (80–120 mg each) | MDMAAP | Inactive placebo | 2 months after treatment | CAPS-5, SDS | Reduced symptomatology and disability |
| Wolfson et al. ( | 18, LTI | RCT | 3, MDMA (125 mg) | MDMAAP | Inactive placebo | 1 month after second MDMA session | STAI | Reduced trait anxiety |
| Sessa et al. ( | 4, AUD | Pre-post | 2, MDMA (187.5 mg for each session) | MDMAAP plus elements from MET and third wave CBT | None | 9 months | PHQ-9, GAD-7, SADQ, SIP | Improved psychosocial functioning, reduced in alcohol consumption |
| Dakwar et al. ( | 40, AUD | RCT, pilot | 1, ketamine ( | MET | Midazolam | 21 days after infusion | Abstinence, time to relapse, heavy drinking days, | Significantly better abstinence rate, time to relapse, heavy drinking days in ketamine group |
| Bogenschutz et al. ( | 10, AUD | Open label | 1 or 2, psilocybin (0.3 mg/kg, 0.4 mg/kg) | MET plus preparation and integration | None | 9-month follow up | Abstinence rates and % of drinking and heavy drinking days | Improved abstinence rates after psilocybin session (s) and reduced drinking and heavy drinking days |
| Carhart-Harris et al. ( | 20, TRD | Open-label | 2, psilocybin (10 mg, 25 mg) | PSI | None | 1 week, 3 and 6 months | QIDS | Improved depression at all timepoints |
| Anderson et al. ( | 18, demoralization | Open-label | 1, psilocybin (0.3 mg/kg) | SEGT | None | End of treatment and 3-month follow up | DS-II | Improved demoralization at the 3-month follow up |
| Pradhan et al. ( | 20, PTSD | RCT | 1, ketamine (0.5 mg/kg) | TIMBER | Inactive placebo | 3 months after drug session | PCL, CAPS | Better and more sustained response |
AUD, Alcohol Use Disorder; BDI, Beck Depression Inventory; BDI, Beck Depression Inventory; CAPS, Clinician Administered PTSD Scale; CBCT, Cognitive Behavioral Conjoint Therapy; CBT, Cognitive Behavioral Therapy; CSI, Couples Satisfaction Index; DS-II, Demoralization Scale II; GAD-7, Generalized Health Questionnaire-7; GAF, Global Assessment of Functioning; HADS, Hospital Anxiety and Depression Scale; HAM-D, Hamilton Rating Scale-Depression; HRTL, Human Relations Training Laboratory; KET, Ketamine Enhanced Therapy; LTI, Life Threatening Illness; MDMAAP, MDMA-Assisted Psychotherapy; MÅDRS, Montgomery-Åsberg Depression Rating Scale; MAP, Medication Assisted Psychotherapy; MDF, Modified Fear Scale; MET, Motivation Enhancement Therapy; MS, Maladjustment Scale; NEO-PI-R, Revised NEO Personality Inventory; PCL, PTSD Checklist; PHQ-9, Patient Health Questionnaire-9; PSI, Preparation Support Integration; PTGI, Post-Traumatic Growth Inventory; QIDS, Quick Inventory of Depressive Symptoms; QIDS, Quick Inventory of Depressive Symptoms; RCT, Randomized Controlled Trial; SADQ, Severity of Alcohol Dependence Questionnaire; SDS, Sheenan Disability Scale; SE/R, Rosenberg Self-Esteem Scale; SEGT, Supportive Expressive Group Therapy; SIP, Short Inventory of Problems for Alcohol; SSSPTSD, Sever-ity of Symptoms Scale for Post-traumatic Stress Disorder; STAI, State-Trait Anxiety Inventory; TAU, Treatment As Usual; TIMBER, Trauma Interventions using Mindfulness Based Extinction and Reconsolidation; TRD, Treatment Resistant Depression.