Actively Recruiting
Attachment and Child Health (ATTACH2) Program Adaptation and Pilot Testing Using Web and Mobile Interfaces
Led by University of Calgary · Updated on 2024-05-10
100
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
The trial investigates the adaptation and pilot testing of the ATTACH2 parenting program, originally designed for in-person delivery, to an online web and mobile format. The program aims to improve children's mental, emotional, and behavioral health by strengthening the parent-child relationship, particularly for families affected by stressors like depression, addiction, domestic violence, and poverty. This transition responds to challenges posed by the COVID-19 pandemic limiting in-person services and seeks to provide safe, user-friendly virtual mental health support to vulnerable families. The ATTACH2 program consists of 10 to 12 weekly sessions, each about 45 minutes, delivered by trained facilitators such as nurses or social workers. The study involves co-designing virtual interfaces with parents and service providers through four phases: user engagement and design exploration, prototyping, software development, and pilot beta testing. The goal is to create a reliable minimum viable product for virtual delivery that incorporates user feedback and meets the needs of families and facilitators. Participants will be involved in pilot testing the virtual program, with assessments conducted before and after the intervention to measure changes in children's mental, emotional, and behavioral health using age-appropriate tools. Parent-child interaction quality will be assessed using the Parent Child Interaction Teaching Scale. Data will be collected through surveys and focus groups, and refinements will be made based on participant feedback. The study also includes dried blood sample collection for participating families in specific locations, and the total intervention period spans about 10 to 12 weeks.
CONDITIONS
Brief Title
Adaptation and Pilot Testing of Web and Mobile Interface for the ATTACH™ Intervention
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Parent of a child between birth and 32 months of age
- Agree to participate in 10 to 12 weekly parent training sessions lasting about one hour each
- Agree to bring a co-parent to 2 to 3 of the sessions when possible
- Agree to provide dried blood samples from self and child (if participating in Calgary agencies)
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person or virtual)
Duration - 10 to 12 weeks
Participants engage in weekly parent training sessions designed to improve Reflective Function (RF) and parent-child interactions using the ATTACH™ program delivered via web and mobile interfaces.
10 to 12 weekly sessions lasting about one hour each, including 2 to 3 sessions with a co-parent
Trial Site Locations
Total: 1 location
1
University of Calgary
Calgary, Alberta, Canada, T2N 1N4
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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