Discovery House
Calgary, Alberta, T2A 7R7, Canada
Location status: Recruiting
NCT Number: NCT04235335
Evaluation of Mother's Empowerment Program and Kid's Club Program adapted specifically for Indigenous mothers and children affected by intimate partner violence in Canada
Interested in participating?
Request Info6 year–13 year
All sexes
Interventional
Not applicable
Calgary, Alberta, T2A 7R7, Canada
Location status: Recruiting
Research Goals & Objectives. Our overall goal is to conduct a feasibility study of two successful evidence-based interventions (Mother's Empowerment Program and Kid's Club Program) designed specifically to meet the needs of Indigenous mothers and their children who have experienced intimate partner violence (IPV).
Specifically, our objectives are:
Hypotheses. We will determine if there is an increase, both immediately post-intervention and sustained over 6-8 months, in mothers' and children's mental (e.g., resilience) and physical well-being (e.g., perceived health status), and if there is a reduction in mothers' and children's mental health (e.g., depression, anxiety and traumatic stress symptoms) and physical difficulties (e.g., somatic symptoms such as headaches). For children, analyses will take age, gender and sex into account.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
-
Weekly groups administered to mothers and children simultaneously but separately for 10 weeks
Time frame: Measured immediately post-intervention
Centers for Epidemiological Studies-Depression (CES-D)
Time frame: Measured 6-8 months post-intervention
Centers for Epidemiological Studies-Depression (CES-D)
Time frame: Measured Immediately post-intervention
Child Depression Inventory (CDI)
Time frame: Measured 6-8 months post-intervention
Child Depression Inventory (CDI)
Time frame: Measured Immediately post-intervention
Beck Anxiety Scale
Time frame: Measured 6-8 months post-intervention
Beck Anxiety Scale
Time frame: Measured immediately post-intervention
Revised Children's Manifest Anxiety Scale - 2nd Edition Short Form (RCMAS-2)
Time frame: Measured 6-8 months post-intervention
Revised Children's Manifest Anxiety Scale - 2nd Edition Short Form (RCMAS-2)
Time frame: Measured immediately post-intervention
PTSD Checklist (PCL-5)
Time frame: Measured 6-8 months post-intervention
PTSD Checklist (PCL-5)
Time frame: Measured immediately post-intervention
University of California - Los Angeles (UCLA) Reaction Index
Time frame: Measured 6-8 months post-intervention
University of California - Los Angeles (UCLA) Reaction Index
Time frame: Measured immediately post-intervention
Adult Resilience Measure - revised (ARM-R)
Time frame: Measured 6-8 months post-intervention
Adult Resilience Measure - revised (ARM-R)
Time frame: Measured immediately post-intervention
Child & Youth Resilience Measure - revised (CYRM-R)
Time frame: Measured 6-8 months post-intervention
Child & Youth Resilience Measure - revised (CYRM-R)
Time frame: Measured immediately post-intervention
Inventory of Socially Supportive Behaviors
Time frame: Measured 6-8 months post-intervention
Inventory of Socially Supportive Behaviors
Time frame: Measured immediately post-intervention
Rosenberg Self Esteem Scale
Time frame: Measured 6-8 months post-intervention
Rosenberg Self Esteem Scale
Contact information is provided by the study sponsor or research team.
Caroline Piotrowski, PhD MPH
CONTACT
Nicole Letourneau, PhD RN
CONTACT
University of Manitoba
Other
Healing Circles: An Evaluation of an Intervention for Canadian Indigenous Mothers and Children Affected by Intimate Partner Violence
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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