TIMBER Psychotherapy and Ketamine Single Infusion in Chronic PTSD

NCT02766192 | Unknown DMC

• 1 other identifier: 13-078
• Study Type: interventional
• Target: 50
• Locations: 1 country
• Sites: 1

Brief Summary

Background: The poor prognosis and public health burden of PTSD necessitates the development of more effective and broader treatment approaches. In the etiopathogenesis of PTSD, trauma memories become ingrained into key brain areas through conditioned learning and are triggered by various situations of daily life. The brain glutamate system plays a key role in the process of trauma learning and trauma memories via long-term potentiation. Ketamine administration modulates the glutamate system and has been used in the treatment of depression and PTSD. Previous studies demonstrate that a single low dose of ketamine rapidly improves symptoms of refractory PTSD and treatment resistant depression. Unfortunately the observed response is short-lived (4-7 days, maximum up to 2 weeks) and multiple doses often produce unacceptable side effects. TIMBER (Trauma Interventions using Mindfulness Based Extinction and Reconsolidation for trauma memory) psychotherapy, is a manualized and translational mindfulness based cognitive behavioral therapy specifically designed to target trauma memories and their expressions in PTSD patients. The placebo controlled pilot study examined the efficacy of a protocol combining a single infusion of low dose ketamine (0.5mg/kg) and TIMBER psychotherapy in subjects suffering from chronic PTSD. The objective of this pilot study was to optimize and individualize treatment of chronic PTSD using a rapid, effective, trauma specific, user friendly and inexpensive approach that uses cutting edge psychopharmacological combined with novel psychotherapeutic approaches. Methodology: The randomized, double blind, placebo-controlled pilot study used a crossover design. Ten subjects with refractory PTSD were assigned to one of two arms: one arm (n=5) received combined ketamine infusion and TIMBER therapy (TIMBER-K arm) and the second (n=5) received combined placebo (normal saline) infusion and TIMBER therapy (TIMBER-P arm). All 10 subjects received a short version of TIMBER therapy after 10 minutes of onset of the infusion in which reactivation of trauma memories was initiated in a controlled manner using standardized scales and scripted narrative of the index trauma. This was followed by a standardized mindfulness based cognitive therapy module to quickly de-escalate the arousal symptoms followed by induction of detached observation and reappraisal of the trauma experience. After completion of the 40-min infusion, all subjects were trained on the full version of TIMBER therapy using methods of mindfulness based graded exposure therapy and a twice-daily schedule of home practice was initiated. The investigators are currently in a process of recruiting fifty more subjects to examine the effects in a larger sample.

Conditions

PTSD

Keywords

ketamine; mindfulness based cognitive therapy; PTSD; trauma memory; memory extinction; memory re-consolidation; metabolomics; TIMBER (Trauma Intervention using Mindfulness Based Extinction and Re-consolidation of trauma memories)

Outcome Measures

Primary Outcomes (2)

• Change from baseline scores on the Clinician Administered PTSD Scale (CAPS) at 25th hours post-infusion

  Response (or Relapse status) was assessed by determining the change from baseline scores on the Clinician Administered PTSD Scale (CAPS) at Days-1 (25th hour post-infusion), 7, 14, 21, 28, 35, 42 and 49 and so on following the initiation of the protocol. This was done in this weekly fashion till 3 months after the infusion. A subject was considered to have relapsed when his/her scores were \>50 in the CAPS scale and \>51 in PTSD Symptom Checklist (PCL) scale respectively. A subject was considered to be a 'Responder' when there was a reduction of 20 or more points of these scores at 25th hours post-infusion compared to his/her baseline scores on CAPS and PCL. To be considered a responder, the response needed to be sustained for 7 days or more.

  For CAPS, change in scores at 25th hour post-infusion compared to the baseline were measured

• Change from baseline scores on the PTSD Symptom Checklist (PCL, self-reported) at 25th hours post-infusion

  Response (or Relapse status) was assessed by determining the change from baseline scores on the PTSD Symptom Checklist (PCL) at Days-1 (25th hour post-infusion), 7, 14, 21, 28, 35, 42 and 49 and so on following the initiation of the protocol. This was done in this weekly fashion till 3 months after the infusion. Both CAPS and PCL scales are used in this study to ensure accuracy and objectivity.

  For PCL, change in scores at 25th hour post-infusion compared to the baseline were measured

Secondary Outcomes (2)

• Change from baseline scores on the Hamilton depression rating scale (17-item version) at 25th hours post-infusion

  For Hamilton depression rating scale, change in scores at 25th hour post-infusion compared to the baseline were measured

• Change from baseline scores on the Beck Anxiety Scale at 25th hours post-infusion

  For Beck Anxiety Scale, change in scores at 25th hour post-infusion compared to the baseline were measured

Study Arms (2)

TIMBER-Ketamine arm

EXPERIMENTAL

This arm received TIMBER psychotherapy and ketamine infusion.

Drug: Ketamine; Behavioral: TIMBER Psychotherapy

TIMBER-placebo arm

PLACEBO COMPARATOR

This arm received TIMBER psychotherapy and placebo (normal saline) infusion.

Behavioral: TIMBER Psychotherapy; Drug: Placebo (normal saline)

Interventions

Ketamine DRUG

TIMBER-Ketamine arm

TIMBER Psychotherapy BEHAVIORAL

TIMBER-Ketamine arm; TIMBER-placebo arm

Placebo (normal saline) DRUG

TIMBER-placebo arm

Eligibility Criteria

• Age: 21 Years - 60 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64)

You may qualify if:

• Men or women, 21-60 years of age;
• Patients attending the outpatient psychiatry clinic of Cooper University Hospital will be screened for this study using DSM-IV diagnostic criteria for PTSD.
• Participants must have a level of understanding sufficient to agree to all tests and examinations required by the protocol and must sign a written informed consent document;
• Participants must fulfill DSM-IV criteria for current civilian or combat-related PTSD, based on clinical assessment by a study psychiatrist, on the self-rated PTSD Check list (PCL-C scores must be at least 51and CAPS score must be at least 50 at screening on the first 17 items of the scale).
• Women must be using a medically accepted reliable means of contraception (oral contraceptive medication etc.) or not be of childbearing potential (i.e., surgically sterile, postmenopausal for at least one year);
• Women of childbearing potential must have a negative pregnancy test at screening and pre-infusion;
• Throughout this study, the participants will be on stable dosage(s) of medication(s).

You may not qualify if:

• Meet criteria for psychotic disorders, e.g. schizophrenia/ schizoaffective disorder.
• Women who are pregnant or are breast-feeding (because the medical risk of using ketamine during pregnancy and breast-feeding are unknown);
• Serious, unstable medical illnesses such as hepatic, renal, gastroenterologic, respiratory, cardiovascular, endocrinologic, neurologic, immunologic, or hematologic disease (including obstructive sleep apnea, history of difficulty with airway management during previous anesthetics, ischemic heart disease and uncontrolled hypertension, and history of severe head injury);
• Clinically significant abnormal findings of laboratory parameters, or physical examination;
• Patients with uncorrected hypothyroidism or hyperthyroidism;
• Histories of mental retardation
• History of one or more seizures without a clear and resolved etiology;
• Drug or alcohol abuse or dependence within the preceding 3 months: phencyclidine (PCP) is especially important in this context because of its resemblance with ketamine not only in structure but also its pharmacodynamic effects on NMDA receptors.
• Previous recreational use of ketamine;
• Diagnosis of schizotypal or antisocial personality disorder (since these are known to reduce the possibility of study completion; other Axis II diagnoses will be allowed).

Sponsors & Collaborators

• The Cooper Health System: lead

Study Sites (1)

Cooper University Hospital

Camden, New Jersey, United States

RECRUITING

Related Publications (2)

• Pradhan B, Kluewer D'Amico J, Makani R, Parikh T. Nonconventional interventions for chronic post-traumatic stress disorder: Ketamine, repetitive trans-cranial magnetic stimulation (rTMS), and alternative approaches. J Trauma Dissociation. 2016;17(1):35-54. doi: 10.1080/15299732.2015.1046101. Epub 2015 Jul 10.

  PMID: 26162001 RESULT

• Pradhan B, Parikh T, Makani R, Sahoo M. Ketamine, Transcranial Magnetic Stimulation, and Depression Specific Yoga and Mindfulness Based Cognitive Therapy in Management of Treatment Resistant Depression: Review and Some Data on Efficacy. Depress Res Treat. 2015;2015:842817. doi: 10.1155/2015/842817. Epub 2015 Oct 5.

  PMID: 26509083 RESULT

Related Links

• Depression Specific Yoga and Mindfulness Based Cognitive Therapy in Management of Treatment Resistant Depression: Review and Some Data on Efficacy.

MeSH Terms

Conditions

Stress Disorders, Post-Traumatic

Interventions

Ketamine; Saline Solution

Condition Hierarchy (Ancestors)

Stress Disorders, Traumatic; Trauma and Stressor Related Disorders; Mental Disorders

Intervention Hierarchy (Ancestors)

Cyclohexanes; Cycloparaffins; Hydrocarbons, Alicyclic; Hydrocarbons, Cyclic; Hydrocarbons; Organic Chemicals; Crystalloid Solutions; Isotonic Solutions; Solutions; Pharmaceutical Preparations

Study Officials

• Basant Pradhan, MD

  Cooper Health System

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Jean Smith, PhD

CONTACT

856-757-7814; jean-smith@cooperhealth.edu

Jean Smith, PhD

CONTACT

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: QUADRUPLE
• Who Masked: PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
• Purpose: TREATMENT
• Intervention Model: CROSSOVER
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: April 11, 2016
• First Posted: May 9, 2016
• Study Start: August 1, 2013
• Primary Completion: December 1, 2017
• Last Updated: May 9, 2016

Record last verified: 2016-05

Locations

US (1)