University Hospital of Psychiatry Zurich, University of Zurich
Zurich, 8032, Switzerland
NCT Number: NCT05902819
An investigation of the effect of matrix-metalloproteinase-(MMP)-9 inhibition with minocycline on the reconsolidation of trauma- or cocaine-related memories
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Notify Me18 year–60 year
All sexes
Interventional
Not applicable
Zurich, 8032, Switzerland
Intrusive memories are involuntary recollections of past emotional events that can become pathological and persist over time, particularly in post-traumatic stress disorder (PTSD) and cocaine use disorders (CUD). Both PTSD and CUD are characterised by a hypersensitivity and -reactivity to cue-elicited memory reactivation and exhibit common neurological alterations, suggesting shared underlying mechanisms. As intrusive memories significantly contribute to maintaining the cycle of relapse in both disorders, it is important to find a way to attenuate them successfully. Research on memory reconsolidation has led to the development of different (pharmacological) approaches to disrupt the process, which have, however, yielded mixed and unspecific effects so far.
The present project aims to investigate the effect of MMP-9 inhibition with minocycline on the reconsolidation of intrusive memories in individuals with CUD or PTSD. Participants will be randomly assigned to a minocycline or placebo group. The study comprises a total of 5 visits during 3 weeks and one follow-up online survey (3 months after the intervention). Participants will receive the study medication before two imagery script-guided memory activation sessions. An ecological momentary assessment (EMA) approach will be employed to track intrusive memories, and glutamate concentration and neural activation will be measured with magnetic resonance spectroscopy (MRS) and functional magnetic resonance (fMRI), respectively, before and after the two imagery sessions.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
General Inclusion Criteria:
Inclusion criteria
for the PTSD group:
Inclusion criteria
for the CUD group:
Inclusion criteria
for the Clinical Controls (PTSD+CUD group):
Exclusion criteria
for the HC, PTSD, CUD, and PTSD+CUD groups:
Exclusion criteria
for Healthy Controls:
Exclusion criteria
for both the PTSD and CUD groups:
Exclusion criteria
for only the PTSD group:
Exclusion criteria
for only the CUD group:
Exclusion criteria
for Clinical Controls (PTSD+CUD group):
Guided imagery of personal trauma- or cocaine-related memory approximately 120min after study medication was given.
Single dose of minocycline (200mg) at each of two imagery sessions; Minocycline is given orally in form of a capsule.
Single dose of mannitol (100%) at each of two imagery sessions; Placebo is given orally in form of a capsule.
Time frame: Changes from baseline intrusive memories frequency and features after both 9 to 39 days (follow-up 1) and approx. 3.5 months (follow-up 2)
Measured with the Intrusion Questionnaire, containing various items on intrusive memories frequency, arousal and distress as well as triggers, and responses.
Time frame: EMA will be conducted for an average of 12 to 42 days (through study participation from baseline to 3 days after follow-up 1).
Captured with a short version of the Intrusion Questionnaire implemented as smartphone-based ecological momentary assessment (EMA), containing items on arousal and distress from self-reported intrusive memories.
Time frame: Change from baseline MRS-measured glutamate concentrations after 9 to max. 39 days (follow-up 1).
Glutamate concentrations are measured using MRS in the amygdala in the PTSD group and in the nucleus accumbens in the CUD group.
Time frame: Changes from baseline fMRI BOLD contrasts after 9 to max. 39 days (follow-up 1).
fMRI BOLD contrasts between conditions (neutral/stress/trauma for the PTSD group; neutral/reward/drug for the CUD group) and between groups.
Time frame: Change from baseline HRV after 9 to max. 39 days (follow-up 1).
HRV will be measured during the fMRI cue-reactivity paradigm (listening to trauma- or cocaine-related narratives compared to trauma- and cocaine-unrelated narratives).
Time frame: Change from baseline respiratory rate after 9 to max. 39 days (follow-up 1).
Respiratory rate will be measured during the fMRI cue-reactivity paradigm (listening to trauma- or cocaine-related narratives compared to trauma- and cocaine-unrelated narratives).
Time frame: Change from baseline subjective distress after 9 to max. 39 days (follow-up 1).
Current subjective distress will be measured with a visual analogue scale before and after listening to trauma- and cocaine-related narratives compared to trauma- and cocaine-unrelated narratives.
Time frame: Change from baseline craving after 9 to max. 39 days (follow-up 1).
Current subjective craving will be measured with the Cocaine Craving Questionnaire (containing ten questions on current craving scaled from 0 to 10) before and after listening to cocaine-related narratives compared to cocaine-unrelated narratives.
Time frame: Change from baseline NfL levels after 9 to max. 39 days (follow-up 1).
NfL levels will be measured in serum samples.
Time frame: Change from baseline sphingolipid levels after 9 to max. 39 days (follow-up 1).
Sphingolipid levels will be measured in plasma samples.
Time frame: Change from baseline inflammatory levels after 9 to max. 39 days (follow-up 1).
Inflammatory biomarker levels will be measured in serum samples.
Time frame: Change from baseline MMP-9 protein levels after 9 to max. 39 days (follow-up 1).
MMP-9 protein levels will be measured in plasma samples.
Time frame: Change from baseline MMP-9 gene expression after 9 to max. 39 days (follow-up 1).
MMP-9 gene expression will be measured in blood samples.
Time frame: Will be measured during 9 to max. 39 days, from baseline until follow-up 1.
Heartrate variability (measured with a wearable (Fitbit)) predicted by the number and quality of intrusive memories experienced. Overall variability per person, in relation to overall health measured at Screening and Baseline as well as pre- and post-intervention variability will be assessed.
Time frame: Will be measured during 9 to max. 39 days, from baseline until follow-up 1.
Sleep duration (in minutes), trajectories over the course of the study periods, clusters of variations in duration and sleep quality (as averaged by the algorithm of Fitbit), according to medication/placebo, number of intrusions and overall health measured at Screening and Baseline.
Time frame: Change from baseline OCCUS score after both 9 to 39 days (follow-up 1) and approx. 3.5 months (follow-up 2).
A 14-item self-report measure that assesses the current inability to control or resist cocaine-related thoughts and behaviors, frequency and impact of thoughts and impulses related to cocaine use, and the degree of interference caused by cocaine related thoughts and behaviors.
Time frame: Change from baseline PCL-5 score after both 9 to 39 days (follow-up 1) and approx. 3.5 months (follow-up 2).
A 20-item self-report measure that assesses the 20 DSM-5 symptoms of PTSD in the last 2 weeks prior to the visit.
Time frame: Change from baseline BDI-II score after both 9 to 39 days (follow-up 1) and approx. 3.5 months (follow-up 2).
A 21-item self-report measure for assessing the severity of depression in the last 2 weeks prior to the visit.
Time frame: Change from baseline PSQI score after both 9 to 39 days (follow-up 1) and approx. 3.5 months (follow-up 2).
A 19-item self-report measure which assesses sleep quality and disturbances in the last 2 weeks prior to the visit.
Time frame: Change from screening GAF score after both 10 to 50 days (follow-up 1) and approx. 4 months (follow-up 2).
A numeric scale used by the investigators to rate the current social, occupational, and psychological functioning of a participants. Scores range from 100 (extremely high functioning) to 1 (severely impaired).
Time frame: Change from screening CAPS-5 score after approx. 4 months (follow-up 2).
A 30-item structured interview that is used to assess the 20 DSM-5 PTSD symptoms, subjective distress, impact of symptoms on social and occupational functioning, improvement in symptoms since the previous CAPS administration, and overall PTSD severity, and specifications for the dissociative subtype.
Time frame: Change from screening IPDC after approx. 4 months (follow-up 2).
A structured interview assessing self-reported patterns of use of common licit and illicit substances during the most representative month of the past year and, in the case of regular cocaine use, also specifically during the past month.
Time frame: Assessed at screening
Voice features and text-based features of reported autobiographical memories recorded during the screening to predict symptoms, with a primary focus on the prediction of intrusion-related features.
Psychiatric University Hospital, Zurich
Other
An Investigation of the Effect of MMP-9 Inhibition With Minocycline on the Reconsolidation of Intrusive Trauma- or Cocaine-related Memories
Acronym: Memocycline
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