Effects of Psilocybin in Post-Treatment Lyme Disease

Sponsor

Johns Hopkins University (Other)

Overall Status

Enrolling by invitation

CT.gov ID

NCT05305105

Collaborator

Steven and Alexandra Cohen Foundation (Other)

Enrollment

Location

Arm

Anticipated Duration (Months)

0.7

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

This study will examine the effects of psilocybin on Lyme disease symptom burden and quality of life in people with Post-Treatment Lyme Disease (PTLD).

Condition or Disease	Intervention/Treatment	Phase
Post-Treatment Lyme Disease Chronic Lyme Disease Lyme Disease, Chronic	Drug: Psilocybin	Phase 1

Detailed Description

This pilot study will evaluate the therapeutic potential of psilocybin in people with well-documented current Post-Treatment Lyme Disease (PTLD). Study measures will assess the impact of psilocybin-assisted treatment on overall symptom burden and quality of life in 20 people with PTLD. This is an open-label proof-of-concept trial in which participants will complete an 8-week course of study treatment including two psilocybin sessions (15mg in week 4 and 15 or 25mg in week 6) with psychological support, and follow-up assessments 1, 3, and 6 months after the final psilocybin session.

Study Design

Study Type:

Interventional

Anticipated Enrollment :

20 participants

Allocation:

N/A

Intervention Model:

Single Group Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

Effects of Psilocybin in Post-Treatment Lyme Disease

Actual Study Start Date :

Jul 1, 2022

Anticipated Primary Completion Date :

Sep 30, 2024

Anticipated Study Completion Date :

Dec 31, 2024

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Psilocybin Participants will complete an 8-week course of study treatment including two doses of psilocybin with psychological support administered approximately 2 weeks apart.	Drug: Psilocybin Dosing at the first session will be 15mg. For the second session participants will either remain at the initial dose, or increase to 25mg.

Arm

Intervention/Treatment

Experimental: Psilocybin

Participants will complete an 8-week course of study treatment including two doses of psilocybin with psychological support administered approximately 2 weeks apart.

Drug: Psilocybin

Dosing at the first session will be 15mg. For the second session participants will either remain at the initial dose, or increase to 25mg.

Outcome Measures

Primary Outcome Measures

Change in multi-system symptom burden as assessed by the General Symptom Questionnaire (GSQ-30) score [Baseline, 2 weeks after final psilocybin dose, 1 month after final psilocybin dose]
The GSQ-30 is a validated and reliable instrument developed to assess multi-system symptom burden among patients with Lyme Disease. Total score ranges from 0 to 120, with higher scores indicating greater symptom burden.
Change in functional health and well-being as assessed by the Short Health Form, Version 2 (SF-36v2) score [Baseline, 2 weeks after final psilocybin dose, 1 month after final psilocybin dose]
The SF-36, version 2 (SF-36v2) is a multi-purpose, short form health survey that yields an 8-domain profile of functional health and well-being scores as well as psychometrically-based physical and mental health summary measures. The number of questions contributing to each domain varies from 2 to 10. Domain scores range from 0 (poorest health status) to 100 (best health status).

Secondary Outcome Measures

Change in fatigue as assessed by the Fatigue Severity Scale (FSS) score [Baseline, 1 week after final psilocybin dose, 1 month after final psilocybin dose]
The FSS was designed to detect and evaluate changes in fatigue over time in persons with chronic illness. Its research utility rests with its ability to measure fatigue severity and identify features that distinguish fatigue between other clinical features of chronic medical disorders, such as depression. Scores on the FSS range from a minimum of 9 to a maximum of 63, with higher scores indicating greater fatigue severity.
Change in pain as assessed by the Short-Form McGill Pain Questionnaire (SF-MPQ) [Baseline, 1 week after final psilocybin dose, 1 month after final psilocybin dose]
The Short-Form McGill Pain Questionnaire (SF-MPQ) was designed to provide a quantitative measure of pain that can be tested statistically and includes major classes of word descriptors used by patients to specify subjective pain experience. The SF-MPQ 15-item pain metric has summary scores ranging from 0 to 45 with a higher score indicating worse pain.

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

≥ 18 years of age.
Capable of providing written informed consent for participation into the study.
Willingness to allow the study team to review past medical records.
At least one current PTLD-defining symptom (widespread pain, fatigue, or neurocognitive dysfunction) following completion of standard, recommended antibiotic therapy for treatment of Lyme disease, and that appeared in the first two years following first evidence of Lyme disease.
Medical record documentation of meeting the Centers for Disease Control (CDC) case definition for clear diagnosis and treatment of early or late Lyme disease while living in a Lyme-endemic area. In other words, a history of physician-documented single or disseminated erythema migrans rash, late Lyme arthritis, or late Lyme neuropathy, OR Medical record documentation of meeting the CDC case definition for probable early or late Lyme disease. In other words, a history of abrupt onset of flu-like symptoms with or without a misdiagnosed rash, and concurrent positive serology while living in a Lyme-endemic area.
Received treatment with a recommended course of antibiotics.
Be medically stable as determined by screening for medical problems via a personal interview, a medical questionnaire, a physical examination, an electrocardiogram (ECG), and routine medical blood and urinalysis laboratory tests.

Exclusion Criteria:

Meeting Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) criteria for moderate or severe substance use disorder (excluding tobacco) within the past 5 years.
Currently taking antidepressants of any drug class, antipsychotics, or Monoamine oxidase inhibitors (MAOIs).
Currently taking lithium or other primary centrally-acting serotonergic medications, whether over-the-counter or prescription (e.g., efavirenz, 5-hydroxytryptophan, St. John's wort).
Cardiovascular conditions: angina, a clinically significant ECG abnormality (e.g. atrial fibrillation or QTc >450msec), transient ischaemic attack (TIA) in the last 6 months, stroke, artificial heart valves, or uncontrolled hypertension with resting blood pressure systolic >139 or diastolic >89, or heart rate >90 bpm.
Renal disease (creatinine clearance < 40 ml/min using the Cockcroft-Gault equation).
Current or past history of meeting DSM-5 criteria for Schizophrenia, Psychotic Disorder (unless substance-induced or due to a medical condition), or Bipolar I or II Disorder.
Family (i.e., 1st degree relative) history of Schizophrenia, Psychotic Disorder (unless substance-induced or due to a medical condition), or Bipolar I Disorder.
Received the Lyme vaccine when it was available (1998-2002).
Development of unexplained chronic pain, chronic fatigue syndrome, fibromyalgia, autoimmune disease, or unexplained neurologic symptoms before first evidence of Lyme disease.
Cancer or malignancy in the past 2 years.
Epilepsy with history of seizures.
Insulin-dependent diabetes; if taking oral hypoglycemic agent, then no history of hypoglycemia.
Current dementia or related disorders including but not limited to, Alzheimer's Disease, vascular dementia, Lewy body dementia, and frontotemporal disorders.
Current or past major immunosuppressive illness or medications.
Currently pregnant or nursing.
Currently of childbearing potential and not using effective methods of contraception.
Not fluent in English.
High risk for suicidal ideation or behavior (i.e., individuals who report suicidal ideation with intent or behavior on the Columbia-Suicide Severity Rating Scale [C-SSRS] at screening, or individuals with a suicide attempt within the past 3 years).