Healing Circles: An Intervention for Canadian Indigenous Mothers & Children Affected by IPV

Sponsor
University of Manitoba (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT04235335
Collaborator
Canadian Institutes of Health Research (CIHR) (Other)
160
1
39

Study Details

Study Description

Brief Summary

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

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Indigenous Mother's Empowerment Program & Indigenous Kid's Club Program
N/A

Detailed Description

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:
  1. To successfully adapt two existing effective evidence-based interventions for mothers and children who have experienced IPV for Indigenous mothers and children who have experienced IPV. Our adaptation process reflects our overall integrated knowledge translation (iKT) approach, undertaken in close partnership with our Community Advisory Council (CAC) and in consultation with Elders at both sites. As outlined by the Canadian Institutes of Health Research (CIHR), it follows a two-eyed seeing approach, incorporating Western and Indigenous knowledge, ways of knowing and being.

  2. To pilot and evaluate our adapted interventions with mothers and children recruited from our community partners (Wahbung Abinoonjiiag, an Indigenous non-profit organization in Winnipeg and Discovery House, a crisis shelter and second stage housing facility for women in Calgary). We plan to evaluate our adapted programs using a two-eyed seeing approach that combines Western (quantitative) and Indigenous (qualitative) methodologies. As part of our iKT approach, our mixed methods evaluation will rely upon ongoing engagement and feedback from our CAC. Quantitative methods (e.g., standardized questionnaires) will be used to assess changes in the mental and physical health and well-being of mothers and their children over time. Qualitative methods (e.g., semi-structured interviews, narratives) will be used to evaluate the intervention experience and perceived changes in self perceptions (e.g., resilience).

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
160 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Healing Circles: An Evaluation of an Intervention for Canadian Indigenous Mothers and Children Affected by Intimate Partner Violence
Anticipated Study Start Date :
Jun 1, 2022
Anticipated Primary Completion Date :
Aug 30, 2024
Anticipated Study Completion Date :
Aug 30, 2025

Arms and Interventions

Arm Intervention/Treatment
Other: Wait List Control

Participants receive intervention after 12 week delay

Behavioral: Indigenous Mother's Empowerment Program & Indigenous Kid's Club Program
Weekly groups administered to mothers and children simultaneously but separately for 10 weeks

Outcome Measures

Primary Outcome Measures

  1. Maternal Depression [Measured immediately post-intervention]

    Centers for Epidemiological Studies-Depression (CES-D)

  2. Maternal Depression [Measured 6-8 months post-intervention]

    Centers for Epidemiological Studies-Depression (CES-D)

  3. Child Depression [Measured Immediately post-intervention]

    Child Depression Inventory (CDI)

  4. Child Depression [Measured 6-8 months post-intervention]

    Child Depression Inventory (CDI)

  5. Maternal Anxiety [Measured Immediately post-intervention]

    Beck Anxiety Scale

  6. Maternal Anxiety [Measured 6-8 months post-intervention]

    Beck Anxiety Scale

  7. Child Anxiety [Measured immediately post-intervention]

    Revised Children's Manifest Anxiety Scale - 2nd Edition Short Form (RCMAS-2)

  8. Child Anxiety [Measured 6-8 months post-intervention]

    Revised Children's Manifest Anxiety Scale - 2nd Edition Short Form (RCMAS-2)

  9. Maternal trauma symptoms [Measured immediately post-intervention]

    PTSD Checklist (PCL-5)

  10. Maternal trauma symptoms [Measured 6-8 months post-intervention]

    PTSD Checklist (PCL-5)

  11. Child trauma symptoms [Measured immediately post-intervention]

    University of California - Los Angeles (UCLA) Reaction Index

  12. Child trauma symptoms [Measured 6-8 months post-intervention]

    University of California - Los Angeles (UCLA) Reaction Index

Secondary Outcome Measures

  1. Maternal resilience [Measured immediately post-intervention]

    Adult Resilience Measure - revised (ARM-R)

  2. Maternal resilience [Measured 6-8 months post-intervention]

    Adult Resilience Measure - revised (ARM-R)

  3. Child resilience [Measured immediately post-intervention]

    Child & Youth Resilience Measure - revised (CYRM-R)

  4. Child resilience [Measured 6-8 months post-intervention]

    Child & Youth Resilience Measure - revised (CYRM-R)

  5. Maternal social support [Measured immediately post-intervention]

    Inventory of Socially Supportive Behaviors

  6. Maternal social support [Measured 6-8 months post-intervention]

    Inventory of Socially Supportive Behaviors

  7. Maternal self esteem [Measured immediately post-intervention]

    Rosenberg Self Esteem Scale

  8. Maternal self esteem [Measured 6-8 months post-intervention]

    Rosenberg Self Esteem Scale

Eligibility Criteria

Criteria

Ages Eligible for Study:
6 Years to 13 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • mothers self-reported experience of past intimate partner violence, English-speaking, with at least one school-aged child
Exclusion Criteria:

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • University of Manitoba
  • Canadian Institutes of Health Research (CIHR)

Investigators

  • Principal Investigator: Caroline Piotrowski, PhD MPH, University of Manitoba

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Caroline Piotrowski, Associate Professor, University of Manitoba
ClinicalTrials.gov Identifier:
NCT04235335
Other Study ID Numbers:
  • H2019:501
First Posted:
Jan 21, 2020
Last Update Posted:
Jan 4, 2022
Last Verified:
Dec 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Caroline Piotrowski, Associate Professor, University of Manitoba

Study Results

No Results Posted as of Jan 4, 2022