Actively Recruiting

Phase Not Applicable
Age: 18Years - 50Years
FEMALE
Healthy Volunteers
NCT05927324

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

Led by University of Lausanne Hospitals · Updated on 2024-08-13

24

Participants Needed

1

Research Sites

78 weeks

Total Duration

On this page

Sponsors

U

University of Lausanne Hospitals

Lead Sponsor

I

International Psychoanalytical Association

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

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

Who Can Participate

Age: 18Years - 50Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • 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
Not Eligible

You will not qualify if you...

  • 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

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Lausanne University Hospital

Lausanne, Canton of Vaud, Switzerland, 1004

Actively Recruiting

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Research Team

D

Daniel S Schechter, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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