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NCT Number: NCT06639061

Neuromodulation of the Hippocampus to Reduce Intrusive Re-Experiencing in PTSD: A Randomized Controlled Trial

The goal of this clinical trial is to learn if non-invasive neurostimulation of memory-related brain areas works to treat intrusive memory symptoms in adults patients with posttraumatic stress disorder (PTSD). It will also learn about the effect of this neuromodulation procedure on reorganization of memory-related brain networks. The main questions it aims to answer are:

Does neuromodulation lower the number of times and the emotional severity participants intrusive memories? Does neuromodulation reduces the overall severity of PTSD? Researchers will compare neuromodulation targeting the hippocampus (a memory-related brain structure) to a control stimulation in an area not related to memory processes to see if hippocampus neuromodulation works to treat intrusive trauma memories and PTSD.

Participants will:

1. Undergo magnetic resonance imaging (MRI) scans before and after neuromodulation to: a) determine a personalized neuromodulation target; and b) to measure changes in brain function from before to after treatment. 2. Receive hippocampus neuromodulation or a control neuromodulation once a week for 5 weeks.

Keep a daily diary of their symptoms and the number of times they experience intrusive trauma memories.

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Key information

Age range

20 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

About this study

Intrusive trauma memories are a hallmark of posttraumatic stress disorder (PTSD), and the least treatment responsive. Thus, revealing neurocognitive mechanisms associated with intrusive trauma memories has been indexed a priority. Prior work shows that targeting hippocampal circuitry modulates functional connectivity among distributed cortical-hippocampal network regions and alters memory performance in healthy participants. In the current clinical trial we test hypotheses on the clinical effects of such stimulation in a two-arms randomized controlled trial: Trauma memory reactivation + targeted hippocampal transcranial magnetic stimulation TMS (R-H-TMS) and Trauma memory reactivation + Control TMS (over the SMA; R-C-TMS). We will test a) Hippocampus seed-based connectivity patterns - revealing the impact of the targeted stimulation on extended memory brain networks; and b) frequency and severity of intrusive memory symptoms. The R-H-TMS vs. R-C-TMS contrast will speak to specificity of the noted effects to hippocampal stimulation.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Aged of 20-65 years.
  • Meet a diagnosis of PTSD according to DSM-5 as tested by a structured clinical interview (Clinician-Administered PTSD Scale for DSM-5 - CAPS-5).
  • CAPS-5 total score greater or equal to 33.
  • Endorsement of intrusive symptoms (flashbacks, nightmares, or intrusive memories) with a frequency of at least 3 times a week.
  • Meeting the accepted criteria for inclusion in an MRI examination.

Exclusion criteria

  • Meeting a diagnosis of Complex PTSD or personality disorder.
  • Psychotic disorder, bipolar disorder, or a developmental neuropsychological disorder (autism, mental retardation).
  • Use of psychiatric medications (except for the medications listed in section 4.a of the study protocol if the medication dosage is stable in the last three months and does not change during the study.
  • Exclusion rules in TMS research (see guidelines).
  • Use of the following drugs: imipramine, amitriptyline, doxepin, nortriptyline, maprotiline, chlorpromazine, clozapine, foscarnet, ganciclovir, ritonavir, amphetamines, cocaine, (MDMA, ecstasy), phencyclidine (PCP, angel's dust), ketamine, gamma- hydroxybutyrate (GHB), alcohol, theophylline
  • Epilepsy or use of anti-epileptic drugs.
  • Traumatic head injuries or head surgery.
  • Implanted metallic body (except fillings/amalgam bites/orthodontic fixations approved for MRI), electrodes or a pacemaker.
  • Migraines
  • Pregnant women
  • Hearing problems
  • Drinking alcohol 24 hours before the TMS session
  • Repeated episodes of fainting with loss of consciousness and/or an event of fainting with loss of consciousness in the past year.
  • The accepted exclusion criteria for an MRI examination

Treatment and study plan

Hippocampal stimulation using repetitive transcranial magnetic stimulation (rTMS)

Device

We will use fMRI resting state data to personalize a TMS inhibitory stimulation to a cortical location that is the most strongly connected to a deeper left hippocampal target.

5 once a week sessions of rTMS will be delivered at 1-Hz stimulation frequency for 15 minutes following trauma memory reactivation.

Other names: TMS, MRI

Sham stimulation using repetitive transcranial magnetic stimulation (rTMS)

Device

We will use fMRI resting state data to personalize a TMS sham stimulation to a cortical location with near zero connectivity to a deeper left hippocampal target. 5 once a week sessions of rTMS will be delivered at 1-Hz stimulation frequency for 15 minutes following trauma memory reactivation.

Other names: TMS, MRI

Primary outcomes

  1. Clinician-Administered PTSD Scale for DSM-5 (CAPS-5) Total score

    Time frame: Baseline, 6 weeks, 3-months

    The CAPS-5 is a 30-item structured interview that can be used to make current (past month or week) diagnosis of PTSD & make lifetime diagnosis of PTSD.

Secondary outcomes

  1. PTSD Checklist for DSM-5 (PCL-5)

    Time frame: Baseline, 6 weeks, 3-months

    The PCL-5 is a 20-item self-reported measured based on the DSM-5 PTSD symptoms and assessing PTSD symptoms endorsement and severity.

  2. Intrusive trauma memories diary

    Time frame: Through study completion, an average of 8 weeks

    The amount, frequency and emotional effect of intrusive traumatic memories, measured by a daily self-report digital diary.

  3. Patient Health Questionnaire - 9 (PHQ-9)

    Time frame: Baseline, 6 weeks, 3-months

    Measures severity of depression symptoms as listed in the DSM-5

Other outcomes

  1. credibility/expectancy questionnaire (CEQ)

    Time frame: Baseline

    Measures treatment expectancies and credibility

  2. fMRI Neuroimaging

    Time frame: Baseline, 6 weeks

    Functional connectivity, indicating the level of synchronous activity of certain brain regions during rest (temporal correlation is usually expressed as a Pearson's r). Derived from the fMRI scans, and compared between the two groups as a function of time.

Study contacts

Contact information is provided by the study sponsor or research team.

Nitzan Censor, PhD

CONTACT

[email protected]

972-3-6406105

Yair Bar-Haim, PhD

CONTACT

[email protected]

972-3-6405465

Sponsors and collaborators

Lead sponsor

Tel Aviv University

Other

Registry information

Official study title

Characterization and Modulation of Traumatic Memories in PTSD Patients Using Transcranial Magnetic Stimulation (TMS)

Important dates

Study start
2024
Primary completion
2027
Study completion
2028
First posted
Oct 15, 2024
Registry last updated
Nov 1, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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