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The Perinatal Synergistic Multi-component Intervention to alLeviate dEpressive Symptoms. A Case Series

Phase 2
Not yet recruiting
Conditions
Postpartum Depression
Interventions
Behavioral: interpersonal psychotherapy (IPT)
Registration Number
NCT06048263
Lead Sponsor
Washington University School of Medicine
Brief Summary

The goal of this open label case series is to learn about the feasibility of conducting a future randomised controlled trial to evaluate how well the Perinatal SMILES intervention works in improving post-cesarean mood in low-income women.

The main questions it aims to answer are:

1. Is it feasible to recruit a sufficient number of participants?

2. Is it feasible to administer Perinatal SMILES and

3. Is it feasible to collect participant outcomes?

To profile EEG in participants at rest and in response to TMS, before and after subcutaneous ketamine

Participants will:

1. Complete five sessions of interpersonal therapy

2. Receive two skin injections of ketamine, approximately 24 hours apart, in the first four postpartum day

3. Receive additional therapy sessions before (to prepare for ketamine) and after (interpersonal therapy) each ketamine injection

4. Undergo assessments of brain electrical activity (at rest and evoked by trans-cranial magnetic stimulation) before and at three timepoints in the 10 hours after each ketamine injection

5. Complete mood assessments over the first 12 postpartum weeks

Detailed Description

The investigators will perform an open-label case series to evaluate the feasibility of performing a trial of a novel intervention to reduce postpartum depression symptoms after cesarean delivery. The intervention, Perinatal SMILES (Synergistic Multi-component Intervention to alLeviate dEpressive Symptoms), combines interpersonal therapy with subcutaneous ketamine therapy. The interpersonal therapy consists of five sessions that will be administered during the antepartum and/or postpartum. The ketamine therapy will be administered as two injections, approximately 24 hours apart, in the first four postpartum days and will be preceded and followed by additional therapy sessions. The investigators will assess brain electronic activity before and after the ketamine injections and mood in the first 12 postpartum weeks. The objective is to determine the feasibility of recruiting participant, administering the intervention and collect the outcome data.

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
Female
Target Recruitment
25
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Intervention Interpersonal psychotherapy plus ketamineinterpersonal psychotherapy (IPT)Five sessions of interpersonal psychotherapy (IPT) and pre-, and post-, ketamine sessions b) Two doses of subcutaneous (SC) ketamine in the first 4 post-cesarean days
Intervention Interpersonal psychotherapy plus ketamineKetamineFive sessions of interpersonal psychotherapy (IPT) and pre-, and post-, ketamine sessions b) Two doses of subcutaneous (SC) ketamine in the first 4 post-cesarean days
Primary Outcome Measures
NameTimeMethod
Depressive symptomsthrough postoperative day 84

These will be assessed using the Edinburgh Postpartum Depression Scale (EDPS) questionnaire.30 The EPDS is a set of ten questions about the subject's mood in the previous seven days. Each symptom is scored on a numeric rating scale of none (0) to severe (3). Commonly employed thresholds for psychiatric referral are 10-13 out of a possible 30 points.

P30 (TMS-evoked potential)4 days

This will be assessed using TMS-EEG. The amplitude of each of component positive (P) and negative (N) deflections in the evoked EEG signal will be recorded before and at 3 timepoints in the 2-10 hours after ketamine. The component deflections are named according to polarity of the deflection (N = negative, P = Positive) and the approximate time in milliseconds after the TMS input. For example N45 is the negative deflection observed approximately 45 ms after the TMS input.

Adverse effects - sedation4 days

Will be assessed on a four point scale (Not present, mild, moderate, severe): sedation.

Adverse effects - diplopia4 days

Will be assessed on a four point scale (Not present, mild, moderate, severe): diplopia.

P60 (TMS-evoked potential)4 days

This will be assessed using TMS-EEG. The amplitude of each of component positive (P) and negative (N) deflections in the evoked EEG signal will be recorded before and at 3 timepoints in the 2-10 hours after ketamine. The component deflections are named according to polarity of the deflection (N = negative, P = Positive) and the approximate time in milliseconds after the TMS input. For example N45 is the negative deflection observed approximately 45 ms after the TMS input.

Cortical evoked activity (CEA)4 days

The CEA will be calculated from the area under the curve of the rectified single pulse TMS-evoked potential

Anxietythrough postoperative day 84

This will be assessed using the General Anxiety Disorder-7 (GAD-7) questionnaire. There are 7 items scored from 0-3. The total score can range from 0 (no anxiety) - 21 (most anxiety).

Psychosocial stressat enrollment 1 day

This will be assessed using the Antenatal Risk Questionnaire (ANRQ). The range of scores is 5-60. A higher score indicates greater psychosocial risk.

Adverse effects - Blurred vision4 days

Will be assessed on a four point scale (Not present, mild, moderate, severe): blurred vision.

N45 (TMS-evoked potential)4 days

This will be assessed using TMS-EEG. The amplitude of each of component positive (P) and negative (N) deflections in the evoked EEG signal will be recorded before and at 3 timepoints in the 2-10 hours after ketamine. The component deflections are named according to polarity of the deflection (N = negative, P = Positive) and the approximate time in milliseconds after the TMS input. For example N45 is the negative deflection observed approximately 45 ms after the TMS input.

N100 (TMS-evoked potential)4 days

This will be assessed using TMS-EEG. The amplitude of each of component positive (P) and negative (N) deflections in the evoked EEG signal will be recorded before and at 3 timepoints in the 2-10 hours after ketamine. The component deflections are named according to polarity of the deflection (N = negative, P = Positive) and the approximate time in milliseconds after the TMS input. For example N45 is the negative deflection observed approximately 45 ms after the TMS input.

Post-Traumatic Stress Disorder (PTSD)through postoperative day 84

The Post-traumatic Stress Disorder Checklist for DSM-5 (PCL-5) questionnaire. Scores range 0 - 80. More severe PTSD scores higher.

Obstetric Quality of Recoverythrough postoperative day 84

(ObsQoR10 score, 10 items, total score 0-100)

Number of participants who successfully breastfeed their newborn baby4 days

Success in any 24-hour period will be defined as when an infant breastfeeds, for 10 minutes or more in a rhythmic suck/swallow/pause/suck pattern, at least eight times in that 24-hour period.

Adverse effects - dizziness4 days

Will be assessed on a four point scale (Not present, mild, moderate, severe): dizziness.

Adverse effects - hallucinations4 days

Will be assessed on a four point scale (Not present, mild, moderate, severe): hallucinations.

Adverse effects - nystamus4 days

Will be assessed on a four point scale (Not present, mild, moderate, severe): nystagmus.

Antidepressant treatmentthrough postoperative day 84

All current pharmacological and psychological therapies will be documented.

Adverse effects - euphoria4 days

Will be assessed on a four point scale (Not present, mild, moderate, severe): euphoria.

Adverse effects - amnesia4 days

Each of the following will be assessed on a four point scale (Not present, mild, moderate, severe): amnesia.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Barnes-Jewish Hospital

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Saint Louis, Missouri, United States

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