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Clinician-Assisted Videofeedback Exposure-Approach Therapy (CAVEAT) Trial (CAVEAT)

Primary Purpose

Post-traumatic Stress Disorder

Status
Not yet recruiting
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
CAVEAT
Sponsored by
University of Lausanne Hospitals
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Post-traumatic Stress Disorder focused on measuring Interpersonal Violence, PTSD, Women, Infants and Children, Attachment

Eligibility Criteria

18 Years - 50 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria: Biological mothers of infants and young children ages 12-54 months Mothers and infants have lived together most of the child's life from the time of birth Exclusion Criteria: Actively psychotic or substance-abusing mothers; Mothers and/or children who are physically or mentally handicapped so as to prevent adequate participation in required research tasks

Sites / Locations

  • University of Geneva Department of Psychiatry--Campus Biotech
  • Lausanne University Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Active treatment

Arm Description

CAVEAT active treatment group

Outcomes

Primary Outcome Measures

Treatment Satisfaction Questionnaire
Parental and Therapist individual self-report questionnaire

Secondary Outcome Measures

Parenting Stress Questionnaire-Short Form
Parental self-report questionnaire
Maternal Attributions Rating Scale
Clinician rating of parental attributions towards the child with scores ranging from 10-50, higher scores representing worse outcome (more negative and age-inappropriate attribution by clinician rating)

Full Information

First Posted
May 30, 2023
Last Updated
July 8, 2023
Sponsor
University of Lausanne Hospitals
Collaborators
International Psychoanalytical Association
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1. Study Identification

Unique Protocol Identification Number
NCT05927324
Brief Title
Clinician-Assisted Videofeedback Exposure-Approach Therapy (CAVEAT) Trial
Acronym
CAVEAT
Official Title
Can Clinician Assisted Videofeedback Exposure Approach Therapy (CAVEAT) Help Post-traumatically Stressed Mothers Change Their Mind About Their Toddlers?
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
September 1, 2023 (Anticipated)
Primary Completion Date
April 30, 2025 (Anticipated)
Study Completion Date
December 31, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Lausanne Hospitals
Collaborators
International Psychoanalytical Association

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The first study proposed is a small (n= 10 to 12 maximum) open feasibility trial of CAVEAT which is a 16-session manualized brief psychotherapy prototcol that is designed to help mothers of infants and young children, whereby the mothers have been exposed to interpersonal violence (i.e. childhood maltreatment and family violence, intimate and non-intimate partner violence, interpersonal combat and or other forms of terrorism or political violence including physical and sexual assault) and who have developed related post-traumatic stress. The treatment uses an integration and extension of evidence-based techniques: Modified Interaction Guidance, Prolonged Exposure Therapy for PTSD, Child-Parent Psychotherapy, and Minding the Baby, in order to help mothers with post-traumatic dysregulation and difficulty in their maintaining sensitivity during challenging parent-child interactions (i.e. when mothers are confronted with child helpless states, emotion dysregulation, negative affect and child aggression). Outcome measures will initially include: maternal attributions towards her child (i.e. perception of child's personality), maternal-child behavior, and maternal-child symptoms of attachment disturbance and PTSD. This feasibility study is meant to perfect the manual and to prepare for an initial open trial with a larger clinical sample including analysis of pre- and post-intervention measures before further randomized control study can be done.
Detailed Description
1. SYNOPSIS OF THE STUDY Sponsor / Sponsor-Investigator Sponsor: Prof. Kerstin von Plessen Sponsor-Investigator: Prof. Daniel S. Schechter Investigator: Mrs. Sandra Rusconi Serpa, MSc, FSP Study Title Feasibility of a brief manualized psychotherapy for traumatized mothers and their young children: Clinician Assisted Videofeedback Exposure Approach Therapy (CAVEAT) Short Title / Study ID CAVEAT Feasibility Study Protocol Version and Date Version 1.0, DATE Study registration Registered on international register (clinicaltrial.gov) provisionally Study category and Rationale This feasibility study conforms to a clinical trial of category A Background and Rationale The present study aims to determine if the manualized brief psychotherapy "Clinician Assisted Videofeedback Exposure-Approach Therapy (CAVEAT)" can be administered to violence-exposed mothers and their young children (ages 1-5 years) in the ambulatory care center of a Swiss public hospital (SUPEA, CHUV) during a psychotherapy of 16 sessions. CAVEAT is based on an amalgam of four existing evidence-based psychotherapy models (Child-Parent psychotherapy, Parental Mentalization, Interaction Guidance, Prolonged Exposure) for parents, infants and young children and traumatized adults that led to the novel, core therapeutic technique developed by Prof. Schechter and colleagues "Clinician Assisted Videofeedback Exposure Session(s) or "CAVES" which has been shown to be successful in positively altering mothers' perception of their young children in two open trials. From the existing literature, the investigataors know that parent-child relationship-based psychotherapies improve significantly maternal sensitivity to their child's communication, which is in part based on maternal capacity to perceive more accurately the young child's emotional communication and to take the child's perspective. Moreover, dyadic psychotherapy models using video-feedback and support of parental mentalization have been shown across models more generally to improve the quality of mother-child interaction. Risk / Benefit Assessment The risks of participating in this study are estimated as minimal (category A). The proposed intervention involves standard, validated psychotherapeutic procedures with the addition of clinician-assisted videofeedback exposure to naturalistic challenges that are typically stressful for young children and that are "in situation" by the clinician in collaboration with the child's mother during the filmed parent-child interaction sessions. This latter technique has been used without complication in both mental health referred and non-referred pediatrics samples with positive clinical effects in both studies. The investigators estimate that the risks of such an intervention are therefore limited. Though, if a matter arises that is severe, urgent or cannot be dealt with in the psychotherapy as conceived in the model, based on the therapist assessment, proper interventions and/or referrals will be made. Regarding the potential benefits An increase in maternal ability to take her very young child's perspective To respond more sensitively to the child's developmental needs and emotional communication, To be aware of what triggers post-traumatic stress during parent-child interactions, Reduction in re-experiencing, avoidance, negative cognitions, and hyperarousal in day-to-day life with one's child Acquisition of increased tools for self and mutual regulation and stress-reduction during are benefits of participating in the study. If this form of manualized psychotherapy proves feasible to administer in a public hospital outpatient mental health clinic for children, it could potentially be implemented for this group of patients in a study that tests its efficacy in terms of improvement in parental stress, maternal sensitivity, and reduction of parent-child relational disturbance, potentially benefitting the larger group of these difficult-to-treat child-parent dyads. Objective(s) The aim of the submitted study is to determine whether the manualized, brief child-parent psychotherapy CAVEAT can be feasibly performed in a child and adolescent psychiatric ambulatory care center at the CHUV, a public university-hospital, this with child and mothers who have experienced IPV and who present to the clinic with concerns about their child's risk for emotional and/or behavior difficulties and/or who note relational disturbances with their very young children ages 1-5 years and/or problems with their parenting. Aim 1: To assess the feasibility of the recruitment procedures and adherence to treatment among patients, mother, and child therapeutic alliance as well as in terms of the mother and child satisfaction. Aim 2: To assess if CAVEAT evaluation measures (questionnaires and observed interactions) will be found appropriate, adequate, and sensitive by patients and therapists to the outcomes targeted Aim 3: To assess if CAVEAT for the therapists is feasible to administer in terms of the application of the psychotherapy manual and the psychotherapy procedures involved to the clinic population. Study Design Open-trial feasibility study. Interim, and post-treatment measures of patient and therapist satisfaction and patient-therapist therapeutic alliance and agreement on treatment goals and realization of treatment objectives. Counts of number of completed sessions and drop-outs before completing the full course of therapy will be noted as well as the clinical supervisor's assessment of therapist adherence to the CAVEAT manual. Statistical Considerations As this is an open feasibility study of 12 participant-dyads only, results will be in terms of descriptive statistics, counts, and percentages. Control Intervention: There is no control group or intervention in this pilot feasibility study. Study procedures As a feasibility study, the present study will implement and check the procedures related to recruitment; inclusion, retention vs drop-out; questionnaire completion and interviews; recording and transcription.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Post-traumatic Stress Disorder
Keywords
Interpersonal Violence, PTSD, Women, Infants and Children, Attachment

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
16 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Active treatment
Arm Type
Experimental
Arm Description
CAVEAT active treatment group
Intervention Type
Behavioral
Intervention Name(s)
CAVEAT
Intervention Description
Brief psychotherapy with mothers of infants and young children, to which infants and young children attend many but not all sessions with mother
Primary Outcome Measure Information:
Title
Treatment Satisfaction Questionnaire
Description
Parental and Therapist individual self-report questionnaire
Time Frame
through study completion, an average of 1 year
Secondary Outcome Measure Information:
Title
Parenting Stress Questionnaire-Short Form
Description
Parental self-report questionnaire
Time Frame
through study completion, an average of 1 year
Title
Maternal Attributions Rating Scale
Description
Clinician rating of parental attributions towards the child with scores ranging from 10-50, higher scores representing worse outcome (more negative and age-inappropriate attribution by clinician rating)
Time Frame
through study completion, an average of 1 year

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Biological mothers of infants and young children ages 12-54 months Mothers and infants have lived together most of the child's life from the time of birth Exclusion Criteria: Actively psychotic or substance-abusing mothers; Mothers and/or children who are physically or mentally handicapped so as to prevent adequate participation in required research tasks
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Daniel S Schechter, MD
Phone
+41213145285
Email
daniel.schechter@unige.ch
Facility Information:
Facility Name
University of Geneva Department of Psychiatry--Campus Biotech
City
Geneva
State/Province
GE
ZIP/Postal Code
1201
Country
Switzerland
Facility Name
Lausanne University Hospital
City
Lausanne
State/Province
VD
ZIP/Postal Code
1004
Country
Switzerland
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Daniel Schechter
Phone
0213148558
Email
daniel.schechter@chuv.ch

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Yes
Citations:
PubMed Identifier
24553738
Citation
Schechter DS, Moser DA, Reliford A, McCaw JE, Coates SW, Turner JB, Serpa SR, Willheim E. Negative and distorted attributions towards child, self, and primary attachment figure among posttraumatically stressed mothers: what changes with Clinician Assisted Videofeedback Exposure Sessions (CAVES). Child Psychiatry Hum Dev. 2015 Feb;46(1):10-20. doi: 10.1007/s10578-014-0447-5.
Results Reference
background
PubMed Identifier
18007960
Citation
Schechter DS, Myers MM, Brunelli SA, Coates SW, Zeanah CH, Davies M, Grienenberger JF, Marshall RD, McCaw JE, Trabka KA, Liebowitz MR. Traumatized mothers can change their minds about their toddlers: Understanding how a novel use of videofeedback supports positive change of maternal attributions. Infant Ment Health J. 2006 Sep;27(5):429-447. doi: 10.1002/imhj.20101.
Results Reference
background
Links:
URL
https://serval.unil.ch/fr/notice/serval:BIB_E777AA5BB11D
Description
Link to CAVEAT concept introduction article (in German)

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Clinician-Assisted Videofeedback Exposure-Approach Therapy (CAVEAT) Trial

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