Clinical trial Recruiting at 1 site Interventional Ages 18 and up

A program to improve emotional awareness and mental health in parents of young children

Official title: Implementing BEAM: An mHealth Tool to Prevent Mental Health Problems and Improve Developmental Outcomes in Young Children

Run by University of Manitoba · NCT06455397 · Data updated 2026-11-12

This study tests a new program that helps parents of young children with depression and anxiety feel better and improve their parenting skills.

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Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment400 (estimated)
SponsorUniversity of Manitoba
Academic / other
Locations1 site (Winnipeg, Manitoba)
StatusRecruiting
StartedMarch 11, 2024
Main results expectedDecember 2026
Study endsJune 2027
Registry record updatedJune 18, 2025
Trial IDNCT06455397 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this program are parents or primary caregivers of children aged 2 to 5 years who are experiencing moderate to severe mental health symptoms.

Probably not a fit

Patients who do not exhibit moderate to severe symptoms of depression, anxiety, or parenting stress may not benefit from this program.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The Building Emotional Awareness and Mental Health (BEAM) program is designed to support parents of young children aged 2 to 5 years who are experiencing moderate to severe symptoms of depression, anxiety, and parenting stress. This innovative mobile health solution aims to improve parental mental health and parenting practices through a combination of virtual check-ins and psychoeducation. The program's effectiveness will be evaluated through an effectiveness-implementation hybrid design, focusing on both the outcomes for parents and the broader impacts on child development. Previous trials have shown promising results in reducing negative mental health symptoms and improving parenting behaviors.

Why it matters

Potential benefit: If successful, this program could significantly enhance the mental health and parenting skills of participants, leading to better developmental outcomes for their children.

How similar studies have gone: Previous studies evaluating similar interventions have shown promising results, indicating that this approach is supported by existing evidence.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Moderate to severe symptoms of depression, anxiety, parenting stress, and/or anger (as measured by the PHQ-9, GAD-7, PSI, and PROMIS-Anger). Those who do not have moderate to severe symptoms will meet with a member of the program research team to determine eligibility. This eligibility decision will be based on clinical judgement, ensuring that those with need can participate.
2. Being a parent or primary caregiver of any gender to an 24- to 71-month-old (i.e., 2-5 year old) child.
3. Living in Manitoba.
4. Able to participate in check ins (15 to 60 minutes) via Zoom, phone, direct messaging with a parent peer coach.
5. 18 years or older.
6. Able to understand/read/speak in English.
7. Willing to complete four 45-min questionnaires.
8. At eligibility screening, a question asks if participants have access to an electronic device for viewing videos and participating in Zoom meetings. Participants who do not have access will be asked to contact the research team. The team may be able to accommodate a limited number of participants by providing relevant devices for the duration of the study.
9. Participants have IP addresses within Manitoba, Canada, as determined by IP address in REDCap at time of eligibility screener questionnaire completion. Participants will be required to securely upload a photo that includes both a valid piece of Manitoba government identification and the participant's face (i.e., a 'selfie').

Exclusion Criteria:

1. Living outside of Manitoba.
2. Being a parent or primary caregiver to a child outside of the ages of 24- to 71-months (i.e., 2-5 years).
3. Previously participated in an earlier BEAM trial.
4. Parents who report self-harm that required medical attention within the past six months or a suicide attempt within the past year will be ineligible to participate in BEAM unless the participant is engaged in individual therapy that attends to this acute risk level with one of the following professionals for the duration of the BEAM program: psychiatrist, psychologist, social worker, or psychotherapist. The research team will email all prospective participants who are pending eligibility to schedule a phone call. This call will determine whether it is feasible to connect the participant with an individual therapist to manage specific needs before engaging in the BEAM program, and discuss if the BEAM program is the right fit for the participant's present needs.

Co-parents will be permitted to participate in BEAM regardless of current mental health challenges. Therefore, co-parents are only subject to inclusion criterion (3) and criteria (5-9). Instead of meeting inclusion criteria (2), parenting partners must be a "co-parent (e.g., the child's mom, dad, step-parent) or other primary caregiver (e.g., the child's grandma, cousin, uncle, auntie)" to the corresponding participant's 24- to 71-month-old (i.e., 2-5 year old) child. Co-parents will not receive the same pre-trial screening as parent participants, and thus will not be subject to exclusion criteria.

Where it's running

  • University of Manitoba - Department of Psychology & Pediatrics
    Winnipeg, Manitoba, Canada
    Recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.