Post-traumatic Stress Disorder Clinical Trial
— CAVEATOfficial title:
Can Clinician Assisted Videofeedback Exposure Approach Therapy (CAVEAT) Help Post-traumatically Stressed Mothers Change Their Mind About Their Toddlers?
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.
| Status | Not yet recruiting |
| Enrollment | 16 |
| Est. completion date | December 31, 2025 |
| Est. primary completion date | April 30, 2025 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | Female |
| Age group | 18 Years to 50 Years |
| Eligibility | 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 |
| Country | Name | City | State |
|---|---|---|---|
| Switzerland | University of Geneva Department of Psychiatry--Campus Biotech | Geneva | GE |
| Switzerland | Lausanne University Hospital | Lausanne | VD |
| Lead Sponsor | Collaborator |
|---|---|
| University of Lausanne Hospitals | International Psychoanalytical Association |
Switzerland,
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. — View 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. — View Citation
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Treatment Satisfaction Questionnaire | Parental and Therapist individual self-report questionnaire | through study completion, an average of 1 year | |
| Secondary | Parenting Stress Questionnaire-Short Form | Parental self-report questionnaire | through study completion, an average of 1 year | |
| Secondary | 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) | through study completion, an average of 1 year |
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