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Parenting Programs for Substance Abuse-related Parent-Child Relationship Issues
N/A
Recruiting
Research Sponsored by University of Ottawa
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up change from pre-intervention to 12 months after engagement and 24 months after engagement
Awards & highlights
No Placebo-Only Group
Summary
This trial will compare two programs for substance-involved mothers to determine if one is more effective in enhancing infant mental health, decreasing child ACEs, and improving parenting attitudes & mother-child relationship.
Who is the study for?
This trial is for English-speaking mothers with a child under 6 years old, who are receiving services at either the Breaking the Cycle (BTC) or Maxxine Wright (MW) programs due to substance involvement.
What is being tested?
The study compares two programs: BTC, which includes infant mental health care, and MW, focusing on mothers. It evaluates effects on children's mental health and mother-child relationships over a period of up to 2 years post-intervention.
What are the potential side effects?
Since this trial involves social and educational interventions rather than medical treatments, traditional physical side effects are not applicable. However, participants may experience emotional or psychological discomfort.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ change from pre-intervention to 12 months after engagement and 24 months after engagement
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~change from pre-intervention to 12 months after engagement and 24 months after engagement
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Children's developmental functioning will be measured using the Ages and Stages Questionnaire-Third Edition (ASQ-3)
Children's socio-emotional functioning will be measured using the Ages and Stages Questionnaire-Social Emotional (ASQ-SE-2)
Secondary study objectives
Children's exposure to risk and protective factors will be measured using a cumulative risk measure (Bondi et al., 2020)
Maternal adverse childhood experiences (ACEs) will be measured using a Maternal ACEs Measure (Felitti et al., 1998; Dube et al., 2003)
Maternal anxiety will be measured using the Beck Anxiety Inventory (BAI)
+8 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Breaking the Cycle Intervention groupExperimental Treatment1 Intervention
Group II: Maxxine Wright Intervention groupActive Control1 Intervention
Find a Location
Who is running the clinical trial?
University of OttawaLead Sponsor
221 Previous Clinical Trials
269,549 Total Patients Enrolled
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Eligibility Criteria:
This trial includes the following eligibility criteria:- I have a child who is under 6 years old.
Research Study Groups:
This trial has the following groups:- Group 1: Breaking the Cycle Intervention group
- Group 2: Maxxine Wright Intervention group
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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